Breast cancer is a cancer type that develops from breast cells. It emerges from the inner lining of the milk ducts or the lobules that render them with milk. The growth of the malignant tumor can spread to other body parts. The vast majority of breast cancer mostly occurs among females. It should be noted that the majority of cases of breast cancer examined until now are because of iodine absence in the breast cells. For females, about 20% of iodine is required and 70% in the thyroid, and the remaining 5% for the rest of the body.
When we talk about the importance of iodine in females, devouring a lot of salt isn’t the right step. As iodized salt is practically the world’s long source of plentiful iodine. When the iodine level reduces, the iodine receptors are blocked by an increased rate of fluoride, chlorine, and bromides present in the water, food, and the environment, resulting in breast cancer.
According to a recent study, researchers have found that molecular iodine determines how it helps to protect women from fibrocystic breast condition, and it’s proven how it attacks breast cancer. Historically, several studies have suggested iodine supplementation to improve breast health, but none of them focused on how it works on FBC cells. Researchers are working their way to recognize the specific MOA that made molecular iodine effective.
The preclinical investigations have proven the MOA and the medical community a reason to revisit the historic research for hints on utilizing molecular iodine to cure and protect women.
Researchers conducted in vitro studies to observe the biochemical interaction on how the molecular iodine affects breast cancer cells and the cells from the fibrocystic breast tissue. Using an MCF10A, a human immortalized mammary epithelial cell line from the fibrocystic breast tissues of a 36-year-old female caucasian, the FBC study used molecular iodine at multiple doses and the growth or the production of the cells were measured. This followed by a gene expression analysis of major valid markers, that are accountable for cell growth and cell death. In this study also, primary human mammary epithelial cells were used from a healthy female donor.
This breast cancer study used the two most common breast cancer subtypes, using fixed breast cancer lines, MCF7 (luminal A subtype) and MDA-MB231 (triple-negative subtype). All of these cells were treated with molecular iodine at different concentrations to calculate the growth of the cells and their death. This is later followed by gene expression analysis of major valid molecular markers, that are primarily accountable for cell growth and death. Primary human mammary epithelial cells were utilized from a healthy female donor.
The results from both of these studies indicate that molecular iodine has significant inhibitory effects on cell growth in both breast cancer and FBC. The new research results also showcase a rapid increase in cell death in breast cancer lines utilized in the study and from the cells of fibrocystic breast tissue.
In the FBC study, gene expression analysis using a quantitative RT-PCR established that cell cycle genes controlling the G1-S phase transition were up-regulated ( meaning an increase in the number of cellular components, such as RNA or protein).
There were so noticeable changes in Cyclin B expression levels that, again, indicated that cells were arrested before entry into cell division. The expression of nuclear hormone receptors PPAR-α and PPAR-γ was up-regulated. The BCL-2, inhibitor of cell death was more, while expression of caspase-3 was reduced, therefore indicating molecular iodine do incite cell death by activating caspase – a cysteine protease that plays a vital role in independent apoptosis.
While in the breast cancer cell line study, gene expression analysis using a quantitative RT-PCR also established that cell cycle genes controlling G1-S phase transition were majorly up-regulated. There were no changes noticed in Cyclin B expression levels, which further suggests that cells were arrested before entry into cell division.
Upregulation is seen in BLC-2, PPAR-α, and PPAR-γ with down-regulation of caspase-3 indicating molecular iodine causes cell death by activating the caspase-independent apoptosis pathway. The mesenchymal-epithelial transition or MET occurrence are recognized by molecular iodine treatment as shown by a sharp increase of GATA3 and E-cadherin and major down-regulation of vimentin in invasive MDA-MB231 cells.
The preclinical research allowed the researcher to under the mechanism that controls the tumor cells’ growth and showcases the significant cellular effects of molecular iodine on breast cancer cell lines. The results indicate a promising effect of molecular iodine on regulating breast cancer EMT differentiation program required for tumor initiation and metastasis.
More studies are to determine the possible impact of molecular iodine in the breast cancer subtypes using the in vitro 3D models. In conclusion, the preclinical data results suggest that administration of molecular iodine must improve the traditional therapies for the treatment of breast cancer and FBC.
Although the use of iodine supplementation has long been used and recognized in clinics across the world, the treatment effects haven’t been successful. It’s mostly because of iodine supplements being either unstable or containing iodine salts, both of which have been said to be ineffective and contain severe harmful side effects.
Only molecular iodine is significantly effective in improving breast health consistently. Using molecular iodine regularly has shown to decrease the sensitivity of breast cells to the proliferative effects of estrogen, resulting in the normalization of breast tissue.
The complication or challenge with molecular iodine is its instability and oxidizing abilities, which prove ineffective to be useful for breast health. At present, we’ve only one formula of I2 that target breast cell is commercially available to all. It is made up of iodide and iodate salts that when exposed to gastric pH react to form molecular iodine.
To a certain extent, it can cause metastasis. Radioactive iodine, however, is an effective cancer treatment type effective for cancer of the thyroid gland. It’s effective as the radioactive iodine from the drink or capsule is soaked into your body and picked up by the thyroid cancer cells, even if it’s spread all across the body. The radiation causes the death of many cancer cells.
Yes! Iodine is required in the body for producing hydrochloric acid (HCL) and reducing HCL acids has been indicated in the development of these cancers. Iodine causes apoptosis (cancer cell death), removal of precancerous and virus-infected cells.
Yes, too much iodine can be harmful to the body. Taking high levels of iodine can lead to similar symptoms of iodine deficiency, including goiter (an enlarged thyroid gland). Increased levels of iodine intake can cause thyroid inflammation and thyroid cancer.
Here are some of the most common symptoms of iodine levels:
After a review of clinical studies, it’s been found that iodine replacement therapy, mostly for people with low levels of iodine, might enhance the tenderness associated with fibrocystic breast tissue. Women who taken iodine have met with very few side effects.
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Hiccups are an unexpectedly common symptom seen in patients having cancer, whether during cancer treatment or in the palliative care setting. Hiiccups causes these sounds due by involuntary clonic spasms of the diaphragm and intercostal muscles due to sudden closure of the glottis. In most cases, they are annoying and usually stop within a few minutes. However, some patients may experience continuing periods of greater than 24-48 hours, these are persistent/chronic/intractable hiccups that last more than 2 months, and up to 10% of the patients having advanced cancer deal with it. These are more common in men compared to women.
Prolonged or persistent may have undesirable effects. These may include:
There are no medical treatments for treating hiccups as these are temporary and get away easily without treatment. Many old and home remedies for hiccups are said to be efficient but may not work on the patient having persistent hiccups, these remedies include:
Other treatments include Chlorpromazine, Chlorpromazine is a dimethylamine derivative of phenothiazine. It acts peripherally by dopamine antagonism in the hypothalamus. It is the only medication approved for the treatment of hiccups by the US Food and Drug Administration, and for many years it has been in use.
Unfortunately, it doesn’t apply to everyone and has adverse reactions like confusion, hypotension, tiredness, nausea, urinary retention, and excessive sleep even in a single dose.
Baclofen is also an effective drug for people suffering from persistent hiccups and has initiation of baclofen resulted in the proper resolution of hiccups in 6 out of 10 patients and showed remarkable improvement in 2 patients. It is suggested to take an amount of 5gm-20gm of baclofen, three times a day.
Gabapentin is also a medication that has shown significant improvement and the hiccups were relieved by oral gabapentin. Baclofen is a gamma-aminobutyric acid (GABA) analog that activates an inhibitory neurotransmitter is thought to help in blocking the hiccup stimulus. It is recommended to take 100 mg of gabapentin three to four times a day.
Nifedipine, a calcium channel blocker, may play a role in reversing the abnormal depolarization in the hiccup reflex arc.1 It has been reported to put an end to persistent hiccups but tends to induce hypotension, which may be especially severe in volume contracted patients or those receiving opioids. A daily dose of 30 to 60 mg of this drug had a significant effect on patients’ hiccups and even stopped the hiccups in 24 hours.
Your doctors would be the best expert to help treat the hiccups directly based on your condition. The most common medication for treating hiccups in cancer patients would be the anti-sickness drug metoclopramide (Maxolon) or a sedative such as haloperidol or chlorpromazine.
Hiccups occur mostly due to irritation of the nerve that controls the diaphragm which can have different reasons behind it. Those might be due to a certain chemotherapy drug used for treating cancer. Other medications that can or cannot be used for cancer-related problems, such as steroids, antibiotics, or anti-nausea medicines.
Medications that are effective in treating long-term hiccups are the following:
Hiccups are one of the side effects of chemotherapy. Intractable hiccups severely affect a person’s resting and eating habits while reducing their quality of life.
Here are some effective tips for curing hiccups-
Here are some of the most common drugs that set our triggering hiccups:
Yes, hiccups can be a sign of serious illness. Make an immediate appointment to see the doctor if your hiccups last more than 48 hours or if the hiccups turn so bothering that they can cause problems with eating, sleeping, or breathing.
Hiccups can happen if a person nears death if they have an underlying health condition or taking a specific medication. Hiccups are a major complication of severe illness due to the effects of treatment medication.
Sugar is a distraction technique that’s effective in treating hiccups, mostly mild ones. Take a spoonful of sugar and let it dissolve on your tongue or tickle the roof of your mouth with a Q-tip or stick your finger in your ears to stimulate branches of the vagus nerve. The overload on other vagus endings will get rid of hiccups.
Yes! The hiccups have a significant tendency to fade away at sleep onset.
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Myeloid Leukaemia (AML) is a rare but intense type of cancer of myeloid cells (white blood cells responsible for strengthening our immune system and fighting infection). The new standard of care for acute myeloid leukaemia is being tested all around the world for effective treatment of its patients.
The latest results from the VIALE-A phase III clinical trial from this summer revealed a 34% decrease in the death risk, by cementing a drug combination that’s been tested around the work. Phase III was a large multicenter clinical trial that was created to establish whether the combination of “Venetoclax ” and “azacitidine” is superior to azacitidine alone. It was a confirmatory study for the patients diagnosed with AML that we’re unable to tolerate intensive chemotherapy.
As Courtney DiNardo, MD, MSCE, Clinical Researcher in the Department of Leukaemia explained that most of the patients with AML are over the age of 65, which is an age where standard chemotherapies are not an ideal option. It has an increasing rate of toxicity and proves less effective. The main intentions of the phases III VIALE-A trail were to have better overall survival (OS) rate. Fortunately, the study was successful in showcasing it.
The response rate was 66% high, which explained that the majority of the people responded better with the regimen of “venetoclax” and “azacitidine”. The overall survival rate improved significantly in patients that have taken this combination. Even the timing of the response, people who studied and went into remission were excessively higher.
The majority of people who received venetoclax and azacitidine together achieved a diminution of severity of AML within the first cycle of the treatment. Or it was several months faster than the prior existing standard of care.
The new medication is completely different and live-changing in the treatment of cancer, especially AML. It’s the first confirmatory, phase II study that’s evident in showing something better from the previous standard of care, from azacitidine or a low dose of chemotherapy. The new treatment has proved that the drug combination has upgraded the outcomes in both remission rates and OS.
There’s been numerous research and study done over the past few decades to improve the outcomes of people with AML. And various other treatments have tried treating the disease but the result has been elusive. AML has remained to be the most common kind of leukaemia in the world with a 5-year survival rate of 28%.
The combination of venetoclax, a first-in-class medicine added with azacitidine showed a great deal of improvement in older patients with AML. Backed with intensive research evidence and real-time effectiveness, this approach suggested being a potent drug combination.
Venetoclax is effective in treating adults with chronic lymphocytic leukaemia or small lymphocytic lymphoma. This medication targets the B-cell lymphoma-2 (BCL-2) protein that prevents some blood cancer cells from dying naturally from the process of apoptosis. It selectively binds to the BCL-2 protein and hinders it from coming in contact with cancer cells, which helps to restore apoptosis.
While Azacitidine is a chemotherapy drug that functions by allowing the bone marrow to grow normal blood cells, decrease the requirement for blood transfusions and kill abnormal blood cells. It’s placed in a class of medications, known as demethylating agents that are designed to target aberrations of DNA methylation patterns linked with cancer onset and progression.
In the double-blind, placebo-controlled, phase III VIALE-A clinical trial, about 433 people who haven’t received any treatment beforehand with AML and ineligible for intensive chemotherapy were randomized to take either a combination of venetoclax (n=286) arm or azacitidine in combination with a placebo arm (n=145).
The final results expected were primarily the overall survival (OS) rate and complete remission rate along with incomplete hematologic recovery in the United States, China, Japan, the European Union, and EU countries. While the secondary results were complete remission (CR) and CR with partial hematologic recovery (CR + CRH).
According to the researchers, people assigned with venetoclax and azacitidine arm combination in the VIALE-A trial have a median survival rate of 14.7 months against 9.6 months for people with the placebo arm.
Moreover, about 66.4% of people who received venetoclax plus azacitidine achieved CR+CRi against 28.3% for the azacitidine plus placebo group.
The safety of the procedure was mostly consistent among the patients with previous studies of venetoclax and azacitidine combination. The most adverse complication of the combined medication was the following:
The most common and severe reactions happened with less than 10% of patients given venetoclax and azacitidine are febrile neutropenia (30%) and pneumonia (17%).
Tumour lysis syndrome (TLS) was recognized during ramp-up in three patients in the venetoclax arm, but none in the placebo arm. As we all know, TLS is a severe complication of venetoclax due to the fast breakdown of cancer cells, often causing kidney failure, death, dialysis, and death.
Complications caused in the trial, however, were temporary, biochemical changes resolved with uricosuric agents and calcium supplements without treatment interruption.
The biggest problem associated with the venetoclax and azacitidine regimen is its toxicity. It’s quite concerning according to the researchers. There’s already more myelosuppression due to lower white blood cell count due to this regimen. If you have neutropenia and neutropenia-related fever, then you must inform your doctors or physicians. But the toxicity is possible to be reduced at its lowest by the physicians.
The management of patients is the key importance when given the combination of the medication. Historically, patience with azacitidine alone didn’t go into remission until the fourth or sixth cycle of therapy. So researchers didn’t do routinely early bone marrows and required no major interventions and kept the patients on cycle due to their low blood counts when they still had leukaemia.
The combination, however, is different as the vast majority of patients go into remission within the first cycle, meaning it’s important to do bone marrow in the first cycle itself. Older patients with AML often have multiple medical conditions at the same time so physicians have to modify the treatment regimen down. Instead of the standard 4 weeks, physicians spread the 21-day regimen over 5 weeks. Doctors have to stop the therapy in between and wait for a week or two for counts to recover, then modify the treatment accordingly.
Monitoring guidelines are developed as a part of the study and available to help the physicians with the management of AML patients acquiring the venetoclax and azacitidine regimen. This drug combination is an incredibly effective regimen that’s well-tolerable if the patients are appropriately managed.
The drug has turned into becoming standard care for older patients with AML, all over the USA. The FDA has also approved the regimen use in 2018, after the phase, I study that gave impressive response rates and the possibility of improvements to overall survival (OS).
After racing the phase III VIALE-A study, the results of the drug combination, this newfound regimen has rapidly adopted the standards of care across the world. There’s still a clinical implication, not just in US citizens but globally. But, this regimen is seen as a practice-changing new therapy globally where the complications can be reduced.
This regime is still an improved standard of care that’s not the same as eliminating the disease. We still need additional research for a new standard of care for AML. This regimen is not helpful for the majority of patients with AML.
Future research sources on the identity of patients with AML that aren’t likely to respond with the combination of venetoclax and azacitidine regimen. Hopefully, it works on people with certain gene mutations that have proved to respond poorly to the regimen.
In the care of TP53 mutations (TP53 is a gene that helps to cease the tumor growth. It acts and is known as a tumor suppressor), effective TP52-treatment to azacitidine and venetoclax that responds safely is still being worked upon.
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Coping with a cancer diagnosis: Emotional & psychosocial effects
A cancer diagnosis is a life-changing event in anyone’s life. It is a destructive disease-causing vita psychological problems among the patients and their family and friends. Psychological agony is a significant and continuing problem for those suffering from cancer who are heavily affected by the time of diagnosis, in the first year after the diagnosis, and commonly during their treatment.
Their mental health needs should be handled with care, but are often ignored as they are not always properly recognized and understood. In the past ten years, there has been a growth in implementing and spreading screening methods for the psychological outcomes of cancer, including depression, anxiety, post-traumatic stress, isolation, hopelessness, distress, and demoralization. Also, guidelines and agencies dedicated to the management of the psychological consequences have been developed and supported by several scientific cancer associations.
By just hearing the word “cancer” said the doctor can have a major effect on a person’s mental and physical health, and relationships with our loved ones. While treating the physical consequences, patients should not ignore the emotional issues related to cancer. One can improve their life by learning more about cancer which may help to make the disease seem less frightening and mysterious.
A patient’s financial, psychological, and social situation may all change due to cancer and its treatment. Here are some of the most common mental effects on a cancer patient:
All of these aspects may be shown in the different phases of the disease from diagnosis to treatment or medical care. Patients tend to adopt variable emotional, cognitive, and behavior toward the disease.
Psychological distress and disorders have magnificent negative effects on the patients and even on their families and loved ones.
TLS usually develops within a few hours to 2-3 days after the start of the chemotherapy. The mortality rate of patients suffering from tumor lysis syndrome is less the 20%
A good social support network has always been associated with an increased and improved quality of life for those patients who are suffering from cancer and undergoing treatment and its distress. Knowing about cancer can make the patient feel less scared and more empowered. Nearly all studies have shown an improvement in physiology for cancer, attending support groups. Social groups help patients in reducing their pain and anxiety.
Screening should be part of care and clinical practice guidelines, these were developed a few years ago and are extremely helpful to clinicians in providing wide-ranging care for cancer patients and their families.
The patient should try to talk openly with the doctors, one of the main reasons why the doctors are unable to distinguish between the general sadness and the severe distress as the patient doesn’t talk openly to the doctors or their caretakers. One-third of cancer patients experience severe distress but about 5-6% can get through it. There is no shame in sharing the problems openly and asking what you need and lack.
Patients should be provided with a healthy and nutritious diet, these improve the physical condition of their body exercise, when possible is important. Studies show that this helps to keep the mind calm, improving memory and concentration, and strengthens the body. This also allows the patient to spend time with others.
It’s okay to feel a certain way at a point in your life. But it’s also healthy and common to express how you feel to your loved ones. Don’t fear expressing strong feelings like anger or sadness, let go of them as much as possible. Talk about your feelings to a close member of your family or friends, or with other cancer survivors and support groups. If you still find it difficult to discuss your condition with others, express your feelings by thinking about why you feel them or write them down.
You are strong and brave. Don’t let any condition weaken your spirit and question your mental health. Most cancer patients tend to blame themselves for getting cancer. Although it’s completely incorrect, even scientists don’t know how a person gets cancer and how someone else doesn’t. All bodies are different and cancer can happen to anyone, from a triathlete to a programmer. It’s not up to us.
It’s always easy to come across a negative when a condition worsens or you are under a problem. It might sound cliche, but life has both dark and light moments. Try to look for the good part of all things even in a bad time or be hopeful rather than thinking the worst. How we perceive the world, the world also becomes the same for us. So try to focus your energy on getting better, and staying healthy as much as possible. Express love to your loved ones for being there with you in misery and fortune. When you start to think of the good, you’ll get many reasons to be happy about in life.
Just because you’ve got cancer doesn’t mean you are helpless. You can completely control and take charge of your life like you did before. Stay involved in your health care, try to learn about the medicines, keep up with your appointments and make good lifestyle changes to turn things better accordingly. Scheduling your day daily is a power move, it gives you a great sense of control. Not just physically, controlling your thoughts can help. Although you can’t control every thought, try not to think about the worse or fearful ones, instead try to look up for the positive things like someones’ birthday, anniversary, next picnic, or a good book.
Don’t try too hard to follow the rules as well. Staying positive and thinking for the best is an ideal way to live but it’s completely normal to feel sad or gloomy once in a while. Have freedom over your feelings.
Cancer is still very unknown to people and often they tend to talk to you about your conditions. It can be overwhelming and tiring to discuss cancer so frequently with every relative or well-wisher you meet. Even when the loved ones mean well, you must let them know what and how you feel about the subject. If you don’t want to discuss them, politely express to them that you are not comfortable talking about them.
Hobbies are always fun to explore. Bring back your old hobbies such as woodworking, reading, art & crafts, paintings, photography, or watching movies, listening to music, or dancing all night. Look for things to enjoy with kids in your family, take your mind off on a fun and interactive tasks.
Relaxing by yourself or doing an activity that helps you unwind and enjoy silence can be a great escape from the chaos that comes with cancer. Try to do relaxing activities such as meditation, exercises, guided imagery, and others to help your body and mind relax and release stress.
Don’t just lie on your bed all day. That won’t help with anything in life. Getting out of your house and going for a little jog, or doing exercise or gentle yoga can keep you fit and active.
Book an appointment with the Best Cancer Specialist at Oncoplus Hospital.
Tumor lysis syndrome ( TLS ) refers to the condition of metabolic disturbance which occurs when a large number of tumor cells or neoplastic cells are killed briskly within a short period, leading to the release of intracellular components in the blood. This syndrome is characterized by the quick development of hyperkalemia, hyperuricemia, hyperphosphatemia, hypocalcemia, with acute kidney injury and is hazardous.
TLS is common in people having blood-related cancer and lymphoma( lymphatic cancer). It initially rises through chemotherapy. Risk factors include tumors with rapid cell growth and movement, hematologic cancers like acute leukemia, or tumors with a high sensitivity to chemotherapy.
Patients with high levels of lactate dehydrogenase (greater than 1,000 U/L) and people with damaged renal function are also at risk. Various chemotherapy agents like cisplatin, etoposide, cytarabine, and paclitaxel are also connected with this syndrome.
Not all cancer patients have an equal rate of developing this syndrome. TLS is most likely to happen when blood disorders and cancer are treated with chemotherapy. In highly reproducing cancer acute leukemia, few cells die before the treatment as it’s the end of their life cycle.
If a huge amount of these cells lyse and die, TLS may grow before the beginning of the treatment. However, a huge amount of intracellular substances are released in the bloodstream as most of the neoplastic cells in the bone marrow and bloodstream of patients suffering from acute leukemia are destroyed through chemotherapy.
These cells get destroyed and die, a large amount of phosphate and potassium are released including purine nucleic acids.
Patients with huge “tumor burdens” (number of cancer cells in the body) or have rapidly dividing cells that respond well with treatment are at high risk. These include:
TLS usually develops within a few hours to 2-3 days after the start of the chemotherapy. The mortality rate of patients suffering from tumor lysis syndrome is less the 20%
The symptoms of these syndromes may be lenient at first, but become hazardous over time due to the mixing of several substances in your systemic circulation. Symptoms of TLS include:
If TLS left untreated, it eventually leads to severe outcomes, these include:
Generally, the first sign of TLS is hyperkalemia and the most dangerous component of this syndrome as potassium tends to leave the cell before they rupture. Hyperkalemia is defined as a medical condition of the body when it has too much potassium in the blood. Potassium is an important nutrient and helps in building nerves, muscles, and the heart.
Mild hyperkalemia is usually asymptomatic but chronic ones can cause a threat to life, cardiac arrhythmias, muscle weakness, or paralysis. This electrolyte can cause lethal dysrhythmias and damage normal cardiac functions. The kidneys aren’t able to excrete enough potassium to remunerate for the hyperkalemia as it is submerged by excess potassium.
Hyperphosphatemia is known as having a high level of phosphate in the blood released from the cancerous cells, phosphate is an electrolyte i.e. electrically charged substance that has phosphorus in it. The kidneys try to get rid of the excess amount of phosphorus in the bloodstream by increasing urine output and decreasing the amount of phosphorus reabsorption, but in the end, it reaches its limits where they can no longer payback, and phosphorus piles up in the blood. Generally, Hyperphosphatemia develops 1-2 days after the treatment.
As phosphate levels increase, phosphate ions (negatively charged) merge with calcium ions (positively charged) eventually leading to decreased serum calcium level. A condition where the body has really less than enough calcium is known as Hypocalcemia. It is also a sign of TLS. These calcium-phosphate complexes cause tubular obstruction and acute renal damage.
Neoplastic cells also release purine nucleic acid. Usually, purines are metabolized to hypoxanthine, converted to xanthine, and then to uric acid by the enzyme xanthine. An excess amount of purines are released rapidly in the blood during this syndrome. The kidneys are unable to excrete the overwhelming amount and results in hyperuricemia and uric acid formation in the kidneys. Hyperuricemia is seen 48 to 72 hours after the beginning of chemotherapy.
Due to these circumstances, the kidneys are submerged by excess phosphorus, potassium, uric acid crystals, and calcium phosphate precipitate leading to acute renal failure. The kidney tries to compensate for the increased electrolyte and uric acid by increasing the urine output, but can’t, due to uric acid nephropathy and volume depletion.
Lab work is carried out every 6 hours for the first 24 hours after chemotherapy started if a patient is in danger due to tumor lysis syndrome.
Clinical signs, lab tests, and symptoms are used in diagnosing the tumor lysis syndrome.
The Cairo-bishop grading system, used in classifying and grading TLS, states lab anomalies in serum uric acid, phosphorus, potassium levels 25% increased over baseline, and serum calcium levels were decreased by 25% from baseline.
This system contemplates lab value alters that occur in patients from 3 days before to 7 days after the beginning of chemotherapy. The lab irregularity organized by the system is categorized based on cardiac dysrhythmias, seizures, severity including age-adjusted serum creatinine.
Tumor lysis syndrome is generally diagnosed by:
One can recover from this life-threatening problem of cancer treatment if they are promptly able to recognize the signs and symptoms of tumor lysis syndrome and take preventive measures.
To help prevent TLS, the following steps you should be taken:
It stops the conversion of xanthine to uric acid and hypoxanthine to xanthine by inhibiting xanthine oxidase. Ideally, it starts 1-2 days before the starting of chemotherapy.
Monitors patients for any fever, allergies, or skin rash including nausea, vomiting, and chills. Common unfavorable results from the intake of allopurinol headache and drowsiness.
Allopurinol therapy is done before chemotherapy as it helps to prevent excess uric acid. It has no effect on patients suffering from hyperuricemia and it increases the level of xanthine that could damage the kidney.
It is never operated with capecitabine because allopurinol may deteriorate its effectiveness.
Rasburicase is a drug that cures hyperuricemia, changes uric acid to allantoin. allantoin is more soluble than uric acid in urine. This drug decreases the level of uric acid and manages the amount of serum potassium, calcium, phosphate, and creatinine.
Also, it works quickly and takes 4-5 hours to show effectiveness. Patients should be well hydrated before taking this drug. Patients with large tumor burdens tend to take longer therapy (up to seven days or twice/day) while for other patients it is effective in 1-2 days.
Pay attention to the patient taking rasburicase while sending lab specimens for the uric acid level test. To maintain approx uric results, the blood samples must be kept on ice after being taken. Poorly ensured samples will give false results because any uric acid of the sample being reduced by rasburicase at room temperature.
Patients receiving this drug should not be supplied with allopurinol as it can interfere in the work of rasburicase and may decrease its effectiveness. Rasburicase should never be given to patients suffering from glucose-6-phosphate dehydrogenase deficiency due to the risk of critical hemolysis.
Stop giving this drug to the patient if it shows a sign of hypersensitivity. Signs of hypersensitivity reactions include bronchospasm, urticaria, dyspnea, chest discomfort, hypoxia, and hypotension. The most common unfavorable reactions of patients related to one dose of this drug infusion are headache, vomiting, and fever. But eventually results in urticaria pruritus, dyspnea, increased liver enzymes, and chest and back pain with increased or repeated dosing.
One can recover from this life-threatening problem of cancer treatment if they are promptly able to recognize the signs and symptoms of tumor lysis syndrome and take preventive measures.
A list of medication, patients suffering from TLS must avoid or there would worsen the effects of this syndrome:
Book an appointment with the Best Cancer Specialist at Oncoplus Hospital.
Covid-19 has shaken the world around us. In these unprecedented times when there’s danger from every side, being a cancer patient can be terrifying. Many cancer patients have suffered from a higher risk of coronavirus due to their withering immunity system. The growing fear, anxiety, and unawareness have taken a toll on everyone’s life, not just on people with cancers. However, we are in this together and united, we can make each other’s life a lot better.
Today, we’ll uncover all the essential information you need to understand between COVID-19 and cancer. And the impacts of covid-19 on cancer patients, caregivers, and treatment options we can take to uncomplicate things.
After reading thousands of articles each claiming to hold new data about this newborn fatal disease, coronavirus isn’t a mystery anymore. It’s an infectious disease caused by a new type of coronavirus. A coronavirus is a group of viruses, each causing some or other health problems. Some cause cold, and flu while the other result in severe damage to breathing or respiratory systems. Depending on your immunity, the virus can or can’t hinder your health.
The most prominent factor of this deadly disease is that it’s contagious, spreading from person to person. It spreads through a sneeze, cough, or by talking or singing loudly. Any type of physical contact with a coronavirus-positive person can lead to spreading to you.
Covid-19 isn’t a piece of good news to anyone, especially not for people with cancers. You are at a higher risk of getting covid-19 if you suffer from cancer. It has a lot to do with the weakened immune system resulting from cancer. Our immune system is highly essential for the protection of the body from foreign damage like viruses, bacteria, and other germs. It battles out numerous infections, and diseases if the immunity is powerful.
More than 89 cancer patients have been subjected to ICU due to covid-19 with a mortality rate of 36%, according to Michael Dang, MD at Memorial Sloan Kettering Cancer Center in New York City. However, there’s a ray of hope, cancer with coronavirus is SURVIVABLE.
The symptoms of COVID-19 to a cancer patient are nothing sort of different from the general population. Here are the symptoms associated with cancer:
If you notice such symptoms in your body, then immediately contact your chemotherapy helpline or the oncology service.
Cancer patients at a higher stage or the most vulnerable ones are extremely at great risk of developing COVID-19. Known as the most vulnerable group. If you identify with it, then as per the government instruction, you must take special preventive measures to ensure your health and immunity strength.
People who are the most vulnerable includes:
Wash your hands: Cleanliness must be the top priority against the covid-19 spread. Regularly wash your hands and at consistent hours. Don’t use soaps, use the hand wash bottles as it’s a much cleaner and safer option. Wash your hands for at least 20 seconds each day and finish it by using a sanitiser.
Avoid Touch: Get rid of touching your face, nose or eyes, as much as it is possible. Public places and areas are equally contagious, like the metro, bus, auto or restaurants while things like elevators, doorknobs require touching, so try to limit it.
Maintain distance: The two meters of long-distance must continue for a long period. Despite it’s at home or a workplace, coming in close contact with anyone can promote the spread of the disease.
Stay Indoors: We can understand the quarantine period was extremely exhausting, both mentally and physically. But to overcome the global pandemic, we must continue staying indoors while protecting each other. So, cancel all non-importance travels and tour plans including your holidays to prioritize your health and safety of others.
Wear a mask: Nothing’s more important than sealing the entrance of the viruses entering your body – the mouth and the nose. You must wear a mask that covers your mouth and nose, properly while stepping out for mandatory work.
The onset of COVID-19 forced various medicare centres to shut. It resulted in a great reduction in cancer screening all this while. Even mandatory measures like cancer screening have ceased to reduce the risk of coronavirus spread among each other. Although for good cause, screening must be done. Fortunately, with things dissolving back to normal and businesses are reopening along with less restriction, you can visit places to do a cancer screening test.
If you’ve missed your screening test then reschedule or talk to your healthcare professionals for better timing. Discussing with your healthcare provider, over a phone call or video chat indicates the risk and benefits of getting a screening in the current environment. Depending on the situation of people and calculating the risk to step outside, helps to decide if you’d want to postpone it or not.
Be careful about your decision as cancer screening is a life saviour, it’s important to get a checkup. Not right now, but after a while, opting for cancer screening must be your top-most priority.
Globally, the only threat to billions of lives is the coronavirus, no matter what weight, race, gender or country you are from. People with cancer are at great risk of getting Covid due to their weakened immunity from cancer and it’s treatment.
If your cancer treatment is complete, then your immune system would take time to recover from its weak condition. People who’ve suffered from cancer in history, are equally, in fact extremely vulnerable groups to acquire COVID-19.
If you notice similar symptoms of COVID-19 in your body, then reach out to your treatment of cancer or oncologist to report and state your condition. There’s no need to panic or worry. Once the doctor comes to know about your situation, you’ll be recommended with the right solution tailored to your needs.
The answer to opting or delaying cancer treatment depends on your situation. Discussing and calculating the risk of COVID-19 with the risk of cancer progression would paint a bigger picture of the importance of seeking treatment. When you weigh the risk and benefits of your situation, treatment timing won’t be a problem anymore.
While calculating the risk, your cancer diagnosis, health, and age play a major factor. If you’re an older adult, that has a slow progression of cancer, then holding off the cancer is a sensible decision, only if you have a communal spread of the virus. But, if you’re much younger and have aggressive cancer development then immediate treatment is the right decision.
Book an appointment with the Best Cancer Specialist at Oncoplus Hospital.
Cancer in children or pediatric cancer is relatively uncommon. Less than 13,500 cases and about 1,500 deaths are reported among kids aged between 0 to 14 years. While more than 1.4 million cases and 575,000 deaths are noted in adults annually. In spite of rare cases, cancer among children remains the 2nd most leading cause of death.
Cancer types that also occur in adults are:
Most common cancers include:
Cancer in children and adults starts when the cell starts to grow out of control and fails to die naturally. These cells further spread to the rest of the body and cause cancer in different areas. The root cause for cancer in both adults and children is the same, but there’s a difference in the type of cancer caused in children and its treatment procedure.
Cancer types in adults differ from the cancers that develop in children. Most cancers develop in adults due to their unhealthy lifestyle and environmental risk which doesn’t happen with children. Only a small number of cancers in children develop due to gene mutation, passed from their parents.
Treatment is most likely to be successful
Most cancers in children respond successfully to certain treatments. It’s a result of different cancer types or due to intense treatments offered to children. In addition, children are free of other health problems than adults that can complicate or worsen with treatment.
Severe long-term complications
There’s an increased risk of side effects on children’s bodies after some types of treatment. For instance, young kids are under a high risk of radiation therapy, and long-term side effects as they are growing.
Here are some of the most common risk factors and causes of cancer in children –
Lifestyle and environmental factors
Unlike adults, lifestyle risk factors like smoking, obesity, lack of exercise, excessive alcohol consumption, and unhealthy eating habits can increase the chances of cancer. It doesn’t apply to children. However, lifestyle factors can take a few years to increase the risk of cancer.
Environmental factors, such as radiation exposure is more lily to increase the risk of cancer in children. Studies also suggest that coming under second-hand exposure to smoking (parental exposure) also increases the children’s risk of developing cancer. Though, there aren’t enough cases that develop from detrimental environmental factors.
Gene Mutation
With extensive studies in gene behavior, scientists have understood the reason behind some changes in the DNA inside our cells that causes it to turn cancerous. DNA is the chemical that makes up our genes and orders the cells on how to function. DNA formation also makes us look similar to our parents. DNA also influences the risk of developing a few diseases, including cancer.
Genes control how our cells grow, reproduce and die. Those genes that help in cell growth division, and keeping them alive are known as oncogenes. While Tumor suppressor genes help to slow down cell division, repair error in cell’s DNA, and cause them to die at the right time. Cancer takes place when the DNA changes by turning on the oncogenes or turning off tumor suppressor genes.
Inherited or acquired gene changes
DNA changes can be inherited from the parents that increase the risk of developing cancer. Gene mutations are present in every cell of children’s body and can be tested through blood tests or other body cells. Any type of DNA change is somewhat linked with the risk of cancer, while others can also cause other health and development issues in children.
Inherited DNA changes aren’t the only cause of pediatric cancer, it can be also acquired in the early stages of the child’s life. Gene changes can develop at infancy or even before birth. When cells divide into two new cells, the DNA is copied to offer the same characteristics. Many times, the cell division doesn’t go correct, and errors take place when the cells are growing rapidly. This kind of gene mutation occurs naturally and at any time of life, known as acquired mutation. Acquired mutation takes place in only individual cancer cells, and will not be inherited by their children.
At certain times, cancer-causing gene changes in adults can be identified, in cause such as cancer-causing chemicals in cigarette smoke. But the cause of DNA changes is still not discovered in pediatric cancer. Some causes like radiation exposure and other types show their causes, but there are still to be discovered.
In children, lifestyle changes and other risk factors like smoking don’t play as a significant risk factor, resulting in cancer. Some of the environmental factors like radiation exposure are somewhat associated with increasing the risk of pediatric cancer. In cases of mandatory exposure to radiation is simply required, for instance, to treat a child’s cancer through radiation therapy.
In conclusion, there’s very little chance of preventing cancer in children.
It’s extremely rare to inherit a gene mutation that increases the risk of a certain type of cancer. In those cases, doctors recommend preventive surgery to remove an organ to stop the chances of cancer development in that particular area. But again, this is very infrequent.
Here are some of the well-known measures to detect growing cancer in children.
Going for regular testing or screen in spite of any visible symptoms or not helps to catch an early disease like cancer. Since childhood cancer is very rare, there aren’t enough screening tests available for children to catch cancer, if there are no chances of increased risk.
Inherited gene mutations from parents increase the chance of developing certain kinds of cancer in children. So those kids must be put under careful consideration, and visit regular medical check-ups to become aware of early signs and symptoms.
Cancer in children is mostly recognized in the early stages, either by the kids’ doctor or by the family members. Identifying any signs or symptoms of growing cancer in children is extremely difficult. On top of that, children are most likely to get sick or develop bumps or bruises that conceal the early signs of cancer.
Cancer in children is extremely rare, in spite of that, we must take kids to routine checkups and screen if any unusual signs and symptoms are found. Here are some unusual symptoms found in childhood cancer:
These symptoms are also common among other illnesses such as injury and infection. Still, you must take these signs into consideration and see a doctor know the exact cause.
Pediatric cancer treatment involves the type and stage of cancer. Here is the major type of childhood cancer treatment:
Some type of cancer treatment also has to go with high-dose of chemotherapy, followed by a stem cell transplant. Targeted therapy drugs and immunotherapy, are the new option in cancer treatment in children that are becoming effective in treating some type of cancer.
Palliative cancer helps to resolve symptoms caused by cancer and restore the healthy life of the patient and their families. Cancer in children is never easy to undergo, in the family, there are a growing concern and sensitivity attached to the child. In most cases, cancer in children isn’t cured but the suffering could be resolved.
In such a condition, pediatric palliative care helps greatly with taking comprehensive care, starting from the diagnosis to the treatment. These care programs help with various communities and can be operated at home. It helps families with psychosocial support and pain relief.
Brain cancer affects severely out of cancers in children. More than 500 children are diagnosed with brain tumors annually, leading to 34% of death.
The chances of cancer in children can’t be determined, though cancer is the second most cause of death in children.
The most common symptoms of leukemia are:
The real cause of cancer in children is still unknown. However, environmental factors and inheritance play a big role.
What is the survival rate of childhood cancer?
Survival rates are determined based on cancer types and various other factors. The survival rate of pediatric cancer has increased, about 84% of children survive for 5 years and more.
Book an appointment with the Best Cancer Specialist at Oncoplus Hospital.
To understand cancer start, growth, and spread, we’ve got to study the smallest constituent first of the body – the cell. We constitute up to trillions of cells formed together into tissue and organs. The cells divide, work, grow, and die from the instruction of the genes present inside the nucleus of each cell. If our cells continue to follow the timely routine of division, growth, and death then we continue to stay healthy.
If there’s any change or damage done to the DNA, our genes can mutate. The damaged genes don’t function properly as the instruction from their DNA is all mismatched. That leads to abnormal changes in the cell, causing the cells to divide and grow out of control that can lead to cancer. Though our immune system handles abnormal smell growth in the body, once cell DNA is damaged, it rapidly reproduces and spreads all over the body. The cancerous cells don’t die when it’s the right time, and continue to grow and divide, forming tumors. Their out-of-control rise affects the surrounding tissues causing complete havoc in the body.
When there’s a proper gene development, our cells are instructed to grow and divide timely. We get the same companies of cells when cells tend to divide. There are 2 identical cells from one cell, then those 2 cells divide into 4, and so on. For cells to normally grow and device into more cells takes place when the body requires them, to replace damaged or replace aging cells.
Cancer cells are however different. These cells have gene mutations that turn the normal cell into cancerous cells. The gene mutation in the cells can be inherited, developed over time as we turn old, or happens when you come in contact with things that are capable of damaging the genes like cigarette smoke, the sun’s ultraviolet (UV) radiation, or alcohol consumption.
Cancerous cells are indifferent to normal cells in terms of growth and division. These cells start to grow and divide abnormally, without any control instead of dying and growing to replace those. These cells also remain immature as they don’t tend to mature as much as normal cells. The most primary reason for cancer is mostly due to cells out of control and inadequate growth and vision. Cancer can take place in any cell of the body.
Due to gene mutations in cancer cells, the cells don’t tend to grow normally as they should rather they grow out of control and don’t die at the right time. Which causes unwanted cells to grow all over the body. Normal cells grow sufficiently and die when they mature while cancer cells continue to grow despite enough cells present.
Here’s how cancer cells differ from normal cells:
The wild growth of cancerous cells forms into a tumor. Similar to normal cells, cancer cells also share the same needs. A regular blood supply brings oxygen and nutrients that help the cells to grow and survive. In the case of a tumor, when it’s very small, it tends to grow easily and soaks oxygen and nutrients from the surrounding blood vessels. But when the tumor turns big, it requires oxygen and other nutrients for the cancer cells in abundance.
In need of more oxygen, the cancer cells indicate a tumor to create new blood vessels. The process is known as angiogenesis and it is a significant reason why the tumor grows and expands all over the body. It also creates a tract for the cancer cells to get into the blood and spread effortlessly to the rest of the body. Studies and ongoing research help to cease the growth of blood vessels using drugs and other medication, called angiogenesis inhibitors, prompting the tumor to stop growing or possibly shrink.
As the tumor grows bigger, the cancerous cells takeover the surrounding tissues and structures by forcing a normal tissue beside the tumor. These cells also produce enzymes that collapse the normals cells and tissues from growth. When cancer affects the nearby or surrounding tissue, it’s known as local invasion or invasive cancer.
Cancer can also travel to the rest of the body from one single spot. It is called metastasis. It happens when the cancer cells detach themselves from the tumor and travel to new areas of the body through the blood and lymphatic system.
Does cancer have any specific area of spread? Yes, most cancers tend to spread to a certain location of the body. Which proves quite helpful to medical practitioners to work out the staging system. Different stages in cancer suggest the spread of cancer from where it started to where it is at presently. Most cancers categories the staging system into 1 to 4 stages, known and written in the Roman numerals I, II, III, and IV.
Understanding how and where cancer spreads helps the doctor examine where it grows further. Ultimately, helping them to plan a full-proof treatment and offer proper support to the patient. Though cancer can originate at any location of the body, it is most likely to spread to the bones, lymph nodes, brain, liver, or lungs.
As mentioned earlier, cancers are classified into different stages based on the size of the tumor and how far it has made into the body. Once you identify the stage of cancer, it helps to break down the suitable treatment for the patient.
However, there’s a different staging process known for certain types of cancer than the I, II, III, and IV type. Here are the basic stages are known in cancer:
In situ stage tells that the cancer is confined to its original site and hasn’t yet invaded the surrounding tissue or spread elsewhere.
Or
Now, the more advanced staging system of TNM is used to articulate the cancer stage. Here’s what your pathology report contains key letters denoting the following message:
Your report would be written by the observation noticed in your body using the above letters. It is more detailed and informative about the cancer growth that helps with seeking timely treatment and care.
Cancer is also likely to make a comeback, even long after it’s gone. This phase is known as recurrence. Even if a single cancer cell survives in the body post-treatment, the cells proceed to grow and divide rapidly and form a new tumor once again. Cancer can begin at the spot it initially started or spread through the blood or lymphatic system to the rest of the body, forming a new tumor around.
For this reason, doctors perform another treatment right after the first one to ensure complete eradication of cancer, by giving chemotherapy after surgery. It is known as adjuvant therapy. It focuses on treating cancer thoroughly to avoid the risk of it returning. In a few cases, the provided treatment stops working or shows it affects the cancer cells to become more active.
Now, the cancer cells that were on the verge of disappearing or shrinking begin to grow and spread, rapidly. It happens when the genes present in the cancer cells mutate. Treatments like chemotherapy work no longer on mutated genes of cancer cells. If you are unaffected by cancer treatment, your doctor would recommend another treatment that’ll suit your case.
The cycle of cancer starts, growth and spread to the body is extremely rapid. By classifying itself into different stages, doctors can identify cancer development in the body, thereby coming up with befitting treatment. If you notice any early changes in your body, it is highly recommended to get an instant check-up or consult a doctor.
Book an appointment with the Best Cancer Specialist at Oncoplus Hospital.
Which is worse, cancer or chemo? Cancer in itself is a life-altering disease but despite the danger of this disease, its treatment is considered much worse. Is chemotherapy tougher than cancer? Although the treatment is always a better choice than none increasing evidence shows up about chemotherapy not being the right choice. What makes chemotherapy not an ideal choice of treatment anymore, is it unbearable? Let’s find out.
Chemotherapy is one vital treatment procedure for many types of cancer around the world. It includes the use of drugs to kill cancerous cells. It is useful in stopping the growth, division, and reproduction of cancer cells in the body. Just like other cancer treatments, chemotherapy also has significant side effects that are difficult to deal with for most people. Side effects of chemotherapy vary from person to person.
The drugs of chemotherapy are used on active cells. Active cells are cells that are continuously growing and dividing at the same time. When cancer affects the cell, the cells become more active and reproduce rapidly. The cells are from all parts of the body including your blood, mouth, hair follicles, and digestive system. Chemotherapy drugs are used to destroy the fast-growing cells but these drugs travel throughout the body and also damages the healthy, normal cells that grow fast, too. When healthy cells are affected, it leads to a growing number of side effects in the body.
We can successfully treat and overcome the side effects of chemotherapy. With a medical professional, you can prevent side effects. Nowadays, medications are available of all different kinds to effectively cure the situation. Getting rid of chemotherapy complications is called palliative care or supportive care that is a substantial part of cancer treatment. With the ongoing research and advancement in medical science, scientists are constantly working on developing drugs and treatment ways with fewer complications. Only certain types of chemotherapy cause a greater number of side effects while many other types of chemotherapy side effects are easier to tolerate.
All drugs have their type of side effects. Chemotherapy also involves different side effects varying from person to person. Your side effects can be different from the other place, we’ve mentioned the most common types of chemotherapy side effects. Consult your doctor immediately if you ever experience side effects.
Chemotherapy causes a handful of physical problems for a short period. It includes:
Body pain such as muscle, stomach, or headache fades away after a while but nerve damage worsens with every dose. It turns so extreme that the drug responsible for nerve damage is put to stop use. It can take months, even years for nerve damage to come to end, in a few cases, it never goes away.
To treat the side effects, treatments differ based on the problem that is causing it. It’s vital to discuss the pain with your oncologist while you are taking chemotherapy. Sometimes, the problem can arise from cancer itself, not the treatment side effects. If the pain is associated with chemotherapy, the doctor would give pain-killing medication, regulate chemotherapy doses or block pain signals from the nerves to the brains with nerve blocks or spinal treatment.
Your body tunes extremely tired or exhausted most of the time. It’s one of the most common side effects of chemotherapy. From experiencing muscle pain to feeling worn out easily, fatigue causes a lack of concentration and challenges to perform daily tasks. Tiredness is a recurring event even after treatment and lasts about three to four weeks but can go on to two to three months, too.
Loose and watery bowel movements are also an adverse effect of chemotherapy in certain cases. Treating diarrhea at its initial stages can help you from getting dehydrated and also prevent other health problems.
Constipation is also a part of chemotherapy. Lack of optimal bowel movement or difficulty in bowel movement leads to constipation. Use of pain medications or other medicines can also constipate. You can prevent or get rid of constipation by keeping yourself hydrated (drink enough fluids), eat a balanced meal, and do some exercise.
Cells present inside the mouth and throat are also affected by chemotherapy. It develops into hurtful sores in the mouth and throat area, a condition called mucositis. It stays for about 5 to 14 days after the treatment completion. The sores can get infected so don’t share food or come in constant with your family, friends, or children. You can prevent these sores by eating a healthy diet and keeping your mouth and teeth clean. It doesn’t last long, only for a few days, and goes away permanently.
Throwing up and feeling sick to your stomach is a common occurrence in chemotherapy. Such side effects depend mostly on the usage of certain drugs and doses. Intake of dose before and after chemotherapy helps put a stop to nausea and vomiting.
Certain drugs used in chemotherapy can also aim nerve damage. The following symptoms in nerve or muscle indicate damage occurred:
With a lower chemotherapy dose, these symptoms can ease and fade out. However, damage can sometimes be permanent.
Losing hair all over the body is a common part of chemotherapy. Starting from little amounts or in larger chumps, the hair starts to fall out of the scalp. It takes in the first few weeks of chemotherapy and increases rapidly into 1 to 2 months of treatment. Usage of certain drugs and doses cause the risk of hair loss so a decrease in its use can cause hair regrowth.
Certain chemotherapy side effects travel to your heart. It’s always recommended to check the heart before starting the treatment. If there is an existing heart problem, then the treatment can cause additional problems. Echocardiogram, a common test that used ultrasound waves to create a moving picture of the heart.
Many side effects improve with time. However, some complications also return or develop after a while. For example, chemotherapy is prone to cause permanent damage to the heart, kidneys, liver, lung, or reproductive system. While others face cognitive problems, such as difficulty in thinking, focusing, and memory loss for months or years after the treatment.
Many times, kids don’t experience or develop side effects in the month of the year after treatment but these side effects reoccur. Known as late effects, cancer is also likely to return later in life in cancer survivors.
Chemotherapy affects the bone marrow, responsible for making new blood cells in the body. It is characterized as a spongy tissue inside the bones. Chemotherapy causes a shortage of blood cells. Though the blood cell number returns to normal once the treatment stops, the complication caused by fewer blood cells creates a lot of problems in the meantime.
To check any blood disorder, here are the following test done by doctors:
Complete blood count (CBC): This test helps to identify the levels of the red blood cells and white blood cells in the blood. You can develop anemia if your body doesn’t have enough red blood cells. Its symptoms include fatigue, shortness of breath, and dizziness. While a shortage of white blood cells leads to a condition called leukopenia. That increases the risk of developing infections, especially severe ones. Use antibodies immediately if you notice any signs of this condition.
This test includes measuring the number of platelets in the blood. Platelets are very vital for the body as it helps the body against excessive bleeding. By plugging damaged blood vessels and forming clots, platelets are effective in sealing any cut. Shortage of platelets causes a condition called thrombocytopenia that involves excessive bleeding and bruising than normal.
Low blood counts are a risk but can be prevented by adjusting doses of chemotherapy. Medications are also available for treating blood disorders that help to increase the blood cell count in the bone marrow. Thereby preventing leukopenia or anemia in people resolving any type of higher risk.
Chemotherapy also causes cognitive problems such as trouble in focusing or concentrating on things. This phase is known as chemo brain that doesn’t work normally, scientifically known as cognitive changes or cognitive dysfunction.
You won’t feel hungry as you did usually and would eat less. If appetite loss continues after the treatment then you’d lose a lot of weight and turn weak. Lack of nutrition in these difficult times can cause muscle loss and strength and make it difficult to cope up with daily activity.
Cancer treatment can also impact your fertility. In women, the ability to get pregnant and carry a pregnancy while the men’s ability to make a woman pregnant is reduced. Exhaustion and lack of enthusiasm from cancer treatment also affect the ability to enjoy sexual activity. Consider undergoing a Pap test for women before starting chemotherapy that helps to collect a sample of cells from the cervix. An infant or an unborn baby can also be under harm from chemotherapy. In the first 3 months of pregnancy, when the baby’s organs are still forming, the effects can be seen. So, if you become pregnant amid chemotherapy, use effective birth control to survive the severe side effects.
Book an appointment with the Best Cancer Specialist at Oncoplus Hospital.
Our immune system and cancer are correlated and interdependent in times of need. Just like the immune system, other organs work together in our body to maintain its proper functioning and health. The immune system, out of all, is vital for the protection of our body against numerous diseases and foreign bodies like pathogens.
For fighting cancer, our immune system plays a critical role. It is designed in a way to identify native and non-native cells in our body that can cause harm. The system is efficient in protecting from millions of germs and fights viruses and infection. However, the immune system is more than about fighting diseases. Here’s what you need to know about cancer and the immune system.
The immune system works as a “defense” to our body, protecting it against illness and infection caused by bacteria, fungi, viruses, and parasites. When a foreign particle comes in contact with our body, our immune system responds and reacts to it. By restricting it from entering the human body and protecting it from further damage, the immune system is the body’s first line of defense. It is also known as immune response.
The immune system is highly essential to people with cancer. Here are the reasons why:
Certain cells present in the immune system are likely to identify cancerous cells and kill them immediately before their growth. It’s very rare and still not enough to fight cancer altogether. Some treatments use the immune system to fight cancer. Using the two different parts of the immune system, the fight against cancer can be successful. They are:
Also known as innate immunity, this mechanism always comes into play to defunct the body from harmful damage. Innate immunity reacts immediately to a foreign body and remains always prepared for instant action. Their response involves physical, chemicals, and cellular attack against the pathogens, using natural killer cells, dendritic cells, basophils, mast cells, eosinophils, and neutrophils,
Ways of Inbuilt immune protection
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Innate protection can be changed with various defects in our body disturbing the shield. Here’s how complications can occur to damage these natural protection mechanisms.
Certain cancer treatments can also cause such complications and disrupt these protection mechanisms. You can temporarily experience a decrease in the number of neutrophils in the body due to chemotherapy. While radiotherapy to the lungs can damage the mucus and hair-producing cells responsible for destroying bacteria.
It is a type of white blood cell vital for eradicating infection. Neutrophils move to the areas of infection and attach themselves to the attacking bacteria, viruses, or fungi and swallow them up and kill them with chemicals present in their body. Lack of neutrophils in your blood makes you neutropenic.
Cancer treatment like chemotherapy, radiotherapy, and targeted cancer drugs can reduce the number of neutrophils in our blood. Shortage of neutropenic makes you prone to bacterial and fungal infections after cancer treatments.
After cancer treatment, it’s very important to keep these useful points in mind:
Bacterial infections after cancer treatment are quite prevalent and spread from one another. So you must avoid interaction with your family, children, and friends after treatment and take precautions to fight them easily.
This type of immune protection is acquired when the body has already fought its battle with other diseases. Our body becomes prepared and can easily recognize each kind of bacteria, fungus, or virus that steps into the body for the very first time. When a certain type of infection harms your body for the first time, the body finds it easy to fight it when it occurs again. Infectious diseases like measles and chickenpox are the perfect example of diseases that occur to us only once as our body fights it effectively the second time.
Vaccinations are used in this type of immunity. The vaccine is composed of a small amount of protein from a disease, not a harmful one. Using it in the body allows the immune system to identify the disease when it enters again and the immune response acts to immediately stop from getting an infection with any disease or viral infection.
Few vaccines include small amounts of live bacteria or viruses in them. These are live attenuated vaccines. Scientists use advanced viruses and bacteria that stimulate the immune system in making antibodies. Infections don’t occur with a live vaccine.
There are two main types of lymphocytes in the body called B cells and T cells. They are a type of white blood cells involved in the acquired immune response. B and T lymphocytes cells are made from the bone marrow. Similar to other blood cells, these blood cells become completely mature to help the immune system to fight infection and diseases. B cells age in the bone marrow while the T cells mature in the thymus gland. Once they are completely grown, the B and T cells reach the spleen and the mumps nodes to fight infection.
B cells produce proteins called antibodies to fight the invading bacteria and viruses in the body. There’s a different antibody produced to fight different types of germs invading the body. The antibodies attach themselves to the harmful bacteria and viruses which marks it as an invader to the body. Marking it helps the body to identify the danger and plans it for killing it. Antibodies are also equipped in finding and killing damaged cells. B cells are a significant part of the immune system. B cells are fast and react quickly by making antibodies against the invading virus or bacteria when it enters the body again.
Antibodies contain two ends. One end attaches the protein to the outside of the white blood cells. While on the other end attaches itself to the germ or damaged cells to catch and destroy it. The ends of the antibody that sticks to the white blood cells always remain the same, known as the constant end. But the other end of the antibody that sticks to the germs differs, depending on the cell type it needs to identify. Also known as the variable end. Each of the B cells creates antibodies with a different end from other B cells. The cancerous cells are complex and differ from normal cells. Hence some antibodies use variable ends to identify cancer cells and attach to them.
There are different kinds of T cells, known as helper T cells and killer T cells. The helper T cell is responsible to stimulate the B cells to produce antibodies and help the development of the killer cells. The killer T cells destroy the body’s cells that have been damaged by invading viruses and bacteria, preventing them from further growth and reproducing dangerous cells, and infecting others in the body.
Immunotherapy is responsible for treating certain types of cancer. It utilized the immune system to search and kill cancerous cells. Immunotherapy is highly useful in treating cancer as cancer cells as it’s easy to identify cancer cells from normal cells. The immune system is effective in catching and destroying abnormal cells in the body.
Types of Immunotherapy used to treat cancer are the following:
The immune system is potent in keeping our body safe and protected from detrimental viruses, bacteria, and fungi. With changing times and advancements in ongoing technology and research, immune stem can efficiently help in fighting cancer.
Book an appointment with the Best Cancer Specialist at Oncoplus Hospital.