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 Dealing with the Side Effects of Chemotherapy and Radiation

Since many people use a combination of conventional therapies with alternative, we have been asked to provide a list of ways to deal with the side effects of chemotherapy and radiation.  Some suggestions include:

  • Acupuncture can be used to help with nausea and pain
  • THC (the active ingredient in marijuana) is useful for treating cancer pain, chemotherapy-induced nausea and vomiting, and poor appetite/wasting. It can be prescribed in pill form, while some people find relief from smoking marijuana. However, it is illegal in most states, but your doctor may be willing to prescribe it.
  • For nausea, both ginger and caraway seed can often help. Caraway seed can be used to make a tea to be used after radiation treatment. To prevent nausea, hold a slice of fresh ginger in your mouth while undergoing therapy; if you become nauseous, chew on it. Fennel tea calms the stomach and prevents nausea. Acupuncture or an acupressure wrist band may also help.
  • Pressure points on the wrists that can help reduce nausea. There is a special wrist band that uses electrical stimulation of the nerves in the wrist for this by Woodside Biomedical Inc. in Carlsbad, CA at (888)668-6648. However,  do not use it if you have a pacemaker.
  • For pain or burning in the stomach, mix one heaping teaspoon of kudzu or arrowroot in six ounces of water or licorice tea. 
  • Use imagery, visualization and other mind-body techniques to lessen the side effects and stresses of the cancer treatment.
  • Alpha Lipoic Acid, an antioxidant, can help with nerve death-neuropathy
  • Exercise can help with fatigue, nausea, anxiety, and a variety of other ill effects
  • Banana peels can help with planters warts. Cover the warts with banana peels for 7 days and the warts will dry up.
  • Soy Unique is a fermented soy product that can help enhance the immune system and help increase blood counts. It is easily digested and is very nutritious, making it great for those who have trouble eating. It is available at http://www.naha.theshoppe.com/soyunique.htm.
  • Dr. Whitaker recommends a product called Defience PhytoTherapy, a  powdered supplement formulated by oncologist Mitch Gaynor, M.D., of the Strang Cancer Prevention Center in New York City, specifically for patients undergoing chemotherapy and radiation. It contains milk thistle, grapefruit seed extract, N-acetyl-cysteine and other agents that aid in detoxification, as well as soy isoflavones, other immune enhancers, and plant extracts. Patients state that it gives them more energy. It is available from Healthy Directions at (800) 722-8008.
  • Ganoderma can be used as a supplement during chemotherapy or radiotherapy to reduce side-effects such as fatigue, loss of appetite, hair loss, bone marrow suppression and risk of infection. 
  • Propax - www.propax.com - Helps with fatigue associated with chemotherapy
  • Spirulina helps to reduce the side effects of radiation therapy, including weight loss
  • Other immune builders, like colostrum, ImmunoPower, astragalus, MGM3, IP6, and Transfer Factor can also help with side effects by keeping the immune system going without interfering with the treatments.
  • Chinese herbal remedies can be helpful. Go to http://acupuncture.com/Herbology/Chemo.htm for suggestions
  • For hair loss, consider EVP3 from Janbe. Vitamin E prior to beginning chemo can also help. Ice caps (ice cap, cold cap, caps) sometimes retard hair loss from chemotherapy.
  • After the chemo and radiation is over, check with your doctor about adding antioxidants to your diet to build your system back up. (See note about antioxidants below.)
  • Some people use a zapper during treatments to help keep their system going
  • Hydrazine sulfate is an anti-cachexia drug which acts to reverse the metabolic processes of debilitation and weight loss in cancer.
  • For constipation or gas, enzymes such as Beano, probiotics, sena, buckthorn, epsom salts, or high fiber can help, but be sure to check with your physician. Walking also helps.
  • For anemia - B12, beet juice, and shark liver oil can help.
  • For insomnia - try melatonin.
  • For pain - try acupuncture, biofeedback, or hypnosis.
  • For radiation burns, hyperbaric oxygen therapy can help.
  • For the drying effects of chemo, the European University of Chinese Medicine recommends Z02.
  • Diarrhea can also be a problem for some patients. To help control it, try limiting the amount of fat in the diet.
  • Seacure from Proper Nutrition, Inc. is a dietary supplement derived from deep-ocean undenatured white fish that can also help with nutrition and pain. http://www.propernutrition.com/products.html or call 800-555-8868.

There is a belief among oncologists that chemotherapy can be rendered ineffective to varying degrees if the patient ingests antioxidants. They believe this because one of the ways chemotherapy works is by introducing free radicals into
cancerous tissues to destroy them. Accordingly, some cancer doctors tell
their patients NOT to take any antioxidant supplements during treatment. In fact, some doctors refuse to treat patients who are using supplements. There are some researchers that disagree with this and they recommend some supplementation when undergoing chemotherapy including: CoQ10, vitamin B6, vitamin C, and kelp (to provide trace minerals). You should talk to your doctor about this before adding any supplements or herbs to your diet.
 

Two good books on this topic are:

John Boik's book Natural Compounds in Cancer Therapy goes into all the studies that show supplements and antioxidants and herbs may actually help chemo and not hinder it. This is a good one for doctors to consider. An easier read is Dr. Ralph Moss's book Antioxidants Against Cancer

One antioxidant product called "The Amrit Protection herbal formulas (also called Amrit®)" is a combination of 44 ayurvedic herbs. Scientific studies are available at Amrti's website.

A book with some very good suggestions on making chemo and radiation less harmful to the patient and more toxic to the cancer. Read Beating Cancer  with Nutrition by Patrick Quillin. Available at most libraries and bookstores.

The following physician offers pain management for cancer support due to Chemo or Radiotherapy: Walter Young A.P. in Ft. Lauderdale, FL - Phone (954) 564-0038.

One person's success story using herbs and alternative methods in conjunction with chemotherapy is at http://www.healthwell.com/delicious-online/D_backs/Oct_98/cancer.cfm.

Some alternative physicians deal specifically with side effects of radiation and chemotherapy. These include: Dr. Labriola, and Dr. Rountree.

NCI - The National Cancer Institute's website has a page devoted to side effects at http://cancernet.nci.nih.gov/chemotherapy/chemoside.html. Note: Their suggestions are not alternative, but may be helpful to those who are being treated with chemotherapy. 

WebMDHealth has an article on the side effects of radiation therapy and how to cope with the loss of appetite, fatigue, and changes in sleep patterns that often occur. http://my.webmd.ca/content/dmk/dmk_article_57338. Cancer pain is discussed at http://my.webmd.ca/content/dmk/dmk_article_5963020

Always tell your health care provider what you are taking to be sure there are no  undesirable side effects. Chemotherapy patients should check with their doctors about taking angelica, arnica, bogbean, boldo, celery supplements, clove oil, danshen, feverfew, garlic supplements, excessive amounts of ginger supplements, ginkgo, onion supplements, papain, turmeric and willow bark as these might impact some treatments. If you believe the supplements you are taking are benefiting you, encourage your doctor to read one of the books mentioned above.

Bill Misner, Ph.D. has written an article titled Nutritional Interventions for Reducing the Negative Side Effects of Chemotherapy.  This article has some very helpful suggestions.

If you or a loved one has gone through chemotherapy and radiation and you have found ways to deal with their side effects, be sure to email our webmaster with details.

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Do conventional cancer treatments work?

For some kinds of cancer, chemotherapy (as well as radiation therapy) can be life saving. These include acute lymphocytic leukemia of children and Hodgkin's disease, as well as a few others. For other kinds, chemotherapy almost certainly extends life. These include ovarian cancer, some colon cancer, small cell lung cancer, etc. Chemotherapy and radiotherapy may shrink tumors, when that is a medical necessity, and may succeed in relieving pain (such as from bone metastases). For a limited number of types of cancer, the combination of surgery, radiotherapy and chemotherapy have sometimes made a substantial difference in the outcome of treatment.

TYPE OF CANCER CURE RATE*

Choriocarcinoma (low-risk patients) 90
Burkitt's Lymphoma (Stage I) 90
Acute lymphocytic leukemia 60
Hodgkin's disease (stage III and IV) 60
Diffuse histiocytic lymphoma 70
Nodular mixed lymphoma 75
Testicular carcinoma (stage II-III) 70-90
Childhood sarcomas (w/ radiation & surgery) 70-90
Childhood lymphomas 75

*Percent long-term disease-free survival. Source: Cecil's Textbook of Medicine (1988)

In many other cases, chemotherapy (or radiation therapy) is more of a gamble than a proven therapy.

A Heidelberg, Germany cancer biostatistician who spent 10 years as a statistician in clinical oncology, Dr. Ulrich Abel, published in 1990 a groundbreaking book, "Chemotherapy of Advanced Epithelial Cancer", which summarizes all the available direct evidence from randomized studies as to whether chemotherapy extends survival. By "epithelial" Abel means the most common forms of adenocarcinoma-- lung, breast, prostate, colon, etc. These account for at least 80 percent of cancer deaths in advanced industrial countries.

Small-cell lung cancer "is the only carcinoma for which good direct evidence of a survival improvement by chemotherapy exists." But this improvement amounted to a matter of three months! For non-small cell lung cancer there was also some "weak indications" of small benefit.

 

Effectiveness of chemotherapy for the majority of cancers

For other kinds of chemotherapy, the news is far less promising:

Colorectal: no evidence exists that survival is improved by chemotherapy.
Gastric: no clear evidence.
Pancreatic: largest study "completely negative." Longer survival in the control group.
Bladder: no clinical trial done.
Breast: no direct evidence that chemotherapy prolongs survival. Use is "ethically questionable."
Ovarian: no direct evidence, but probably a small advantage from cis-platinum regimens. But non-randomized comparisons "almost worthless for assessment of therapy.
Cervix and corpus uteri: no improved survival.
Head and neck: no survival benefit, but occasional "positive effect" from shrinkage of tumors.

Disillusionment with chemotherapy is mounting within the medical profession. In a lecture, the doyen of French oncologists, Lucien Israel, MD, once said, "One mustn't count blindly on chemotherapy to destroy cancer cells. These sick cells, when they are not eradicated by drugs, can become more and more aggressive and more and more difficult to treat" (quoted in "La Presse" of Montréal,10/26/95).

Dr. Israel has spent nearly 60 years in the cancer field. At one time he was an ardent enthusiast for chemical treatments but has gradually realized that a large number of cancers simply develop a resistance to such drugs. And such resistance is attributable to the toxic stress generated by the treatment itself.

There is simply no evidence for the vast majority of cancers that treatment with these drugs exerts any positive influence on survival or quality of life in patients with advanced disease. The almost dogmatic belief in the efficacy of chemotherapy is usually based on false conclusions from inappropriate data.

The medical establishment ascribes the alleged historical increase in 5-year survival rates over the last few decades to the beneficial effects of chemotherapy. But this is erroneous thinking. Equating cure with 5-year-survival is misleading.

Some of the reasons 5-year survival rates might be better today than years ago include:

  • improvements in early detection
  • stage migration (better diagnosis leads to improved prognosis)
  • better supportive care

It is quite interesting to note that studies have shown that many oncologists would not take chemotherapy themselves if they had cancer.

 

Effects of chemotherapy drugs

Tamoxifen is among the best-selling anticancer drugs in the world. Tamoxifen is not a harmless or non-toxic supplement. It is a powerful and unpredictable agent, with complex and little understood effects on the body's hormonal balance. The drug itself causes endometrial cancer and cancer of the liver in animals.
cancer and Tamoxifen

Tamoxifen has made a small fortune for its manufacturer, ICI, and their American distributor, Zeneca, Ltd. of Delaware.

Most of the 40 or so chemotherapeutic agents cause baldness by producing a weakened hair shaft that breaks off at the scalp. Hair may take years to return to normal.

Nausea and vomiting are common. Such nausea can lead to weakness, weight loss, dehydration and electrolyte imbalance. Other GI effects are infections of the mucous lining, lips, tongue and mouth. Abdominal colic, constipation, diarrhea are all common. Candida (thrush) is found in 13% of patients. Doxorubicin causes esophagus inflammation in 50%.

Toxic drugs leaking from a needle causes skin necrosis. Severe damage to nerves, tendons and muscle can follow. Surgeons treat this by excising the skin, followed by grafts to repair the damage. Radiation recall: skin, trying to heal from radiation burns, reddens and peels again; blisters and oozing follow. 5-FU can even make people burn from normal sunlight.

Busulfan and other drugs cause discoloration of the skin, weakness, inability to eat and weight loss. Doxorubicin causes darkening of fingers and toes. Bleomycin results in weird pigmentation of the trunk. Thiotepa leads to whitening of the eyelids, nail damage, brittleness, loosening and even loss of nail plates.

Most anti-cancer drugs also cause second cancers, especially of the GI tract, ovaries, and lungs. These are nearly impossible to treat. Tumors continue to develop for years. In one study, 17% of survivors developed unrelated cancer up to 15 years later.

 

Immune system damage is almost universal. The whole panoply of blood diseases is seen: thrombocytopenia with its loss of white blood cells which guard against infection; severe bone marrow hypoplasia; inability to synthesize fibrinogen; abnormally long bleeding time; granulocytopenia. Resulting infections can be treated with antibiotics, but these in turn can bring their own set of side effects.

Heart damage can occur weeks, months or years after treatment, signalled by rapid heart beat, shortness of breath, distended neck veins, swollen ankles, an enlarged liver and heart. Up to 30% of high-dose Doxorubicin recipients develop congestive heart failure.

Over 40% of patients experience mouth ulcers, pain and bleeding, which can make eating a torture. Other problems: candida, herpes and viral infections, dry mouth, drooling, painful swallowing. Loss of sensation, muscle pain, weakness and changes in senses and motor skills are common. Methotrexate causes stiff neck, headache, nausea, vomiting, fever and lethargy for up to 72 hours. Paralysis, paraplegia and death have also occurred. Vinblastine and vincristine cause double vision, loss of bladder control, impotence, and paralysis of the bowel wall.

Ear damage and hearing loss are associated with cis-platin, which is being used against testicular, ovarian, cervical, head and neck cancers.

Reproductive organs can be profoundly damaged, resulting in sterility.

Given these almost uniformly bad results, where did the idea originate that chemotherapy is of such benefit in cancer? One reason is because toxic drugs often do effect a response. i.e., a partial or complete shrinkage of the tumor. But contrary to popular opinion, this reduction of tumor mass does not prolong expected survival. Sometimes, in fact, the cancer returns more aggressively than before because killing off 99% of a mass fosters the growth of resistant cell lines.

Chemotherapy came out of World War II mustard gas experiments and it remains poison. The AMA routinely condemns natural cancer treatments as quackery. But isn't it time that it dropped its quackbusting crusade and replaced it with an open-minded investigation of such methods?

Cancer politics

The drug industry controls the cancer field, through their domination of virtually every single cancer research and treatment institution. Thousands of top cancer researchers around the world are on the payroll of a dozen drug companies, and these same drug company executives sit on the Boards of major cancer centers. They also dominate the major oncology organizations. Patients need to know about the dirty politics of the cancer industry!

Drug companies offer doctors pay-offs for enrolling patients in clinical trials.

Mergers are taking place between giant pharmaceutical companies. Enormous monopolies are being formed which will further restrict freedom of choice for patients.

"Scientific" studies of new drugs, funded by huge companies, almost always turn in favorable results and are approved by the FDA. It costs at least $230 million to get full FDA approval for a new drug. Brilliant scientists working independently and without this kind of funding simply can not afford to get their treatments tested and approved.
cancer and money

To date, not a single non-toxic cancer drug has ever been approved by the FDA. If we're serious about curing cancer, we have got to get greed for profits out of the research process!

Studies have shown that physicians spend an average of 1.3 minutes answering their patients' questions. If you think there has got to be a better way to evaluate your options, you are right!

Remember: your only loyalty should be to yourself and your healing process. Your #1 job is to figure out which treatment approaches are the best ones for you, no matter which "camp" they come from. This is what "integrative" cancer treatment is all about. Good treatments from every medical tradition should be used together to form the most effective cancer battle plan possible. Good treatments should be patient-centered, evidence-based, as non-toxic as possible, and humane.

There is much more about non-harmful cancer therapies here. More about the politics of cancer here.

Misspelled Words on this page cancer, censer, cancel, cencel, cansel, censel, cacer, cencer, canser, caner, canel, cainl, cainr, ceiner, ceinel, cance, cence, canse, cense, canc, cenc, cancre, camcer, canecr, cacner, cnacer, acncer, cancr, cncer, ancer,  radiation, radaitiom, radyatiom, ladiatiom, rdiation, ladaitiom, raiation, ladyatiom, radation, radition, radiaion, radiatin, radiatiom, ladiashon, radyaton, ladaision, ladaishon, radyashun, radaition, ladyasion, ladyation, radyashon, radiaton, ladyaton, ladiation, radaiton, ladyashun, ladaition, radiashun, ladyashon, ladiaton, radaishun, radiasion, ladaiton, radiashon, radaision, ladiashun, radaishon, radyasion, ladaishun, radyation, ladiasion, rad1at1on, radiatino, radiatoin, radiaiton, raditaion, raidation, rdaiation, ardiation, radiatio, adiation\, therapy, thelapie, therepie, tehrepie, terapy, tehlapie, thrapy, thelepie, theapy, tehlepie, therpy, theray, therapie, tehrapie, tehlapi, thelepy, tehlepy, therapi, tehrapy, tehrapi, thelapy, thelapi, therepy, tehrepy, tehlapy, therayp, therpay, thearpy, threapy, hterapy, therap, herapy, chmotherapy, chemotherapy, czemutherapie, czemotehrapi, czemothelepy, chemotehlepie, chemotehrapie, cheotherapy, czemothelepie, chemotehlapi, czemuthelepy, chemuthelepie, chemutherapie, chemtherapy, czemotherepie, chemutehrapi, czemotherepy, czemotherapy, chemothelapie, chemoherapy, czemotehrapie, czemotehlepy, czemutherepy, czemothelapy, chemuthelapie, chemoterapy, chemutehrapie, chemutehlepy, czemotehrapy, czemutherapy, chemotherepie, chemothrapy, czemotehrepy, czemotehlapy, czemuthelapy, chemotehrepie, chemotheapy, chemutehrepy, chemutehrapy, czemotherapi, chemutherepie, chemotherpy, czemotherapie, czemutehrapy, czemothelapi, chemotehlapie, chemotheray, cemotherapy, czemothelapie, chemutehlapy, czemutherapi, chemothelepie, chemotherapie, chemuthelapi, chemotherepy, chemotherapi, chemotehrepy, chemotehrapy, chemutherepy, chemotehrapi, chemotehlapy, chemutherapy, chemothelepy, chemutherapi, chemotehlepy, chemothelapy, chemuthelepy, chemothelapi, chemuthelapy, chenotherapy, chemotherayp, chemotherpay, chemothearpy, chemothreapy, chemohterapy, chemtoherapy, cheomtherapy, chmeotherapy, cehmotherapy, hcemotherapy, chemotherap, hemotherapy">
 
Cancer Treatment Information
OncoLink Cancer Resource
A Chemotherapy Primer: Why? What? and How?
Julia Draznin Maltzman, M.D
Abramson Cancer Center of the University of Pennsylvania
Posting Date: November 5, 2003
 

A special note to the reader: all the chemotherapy drugs discussed herein can be found on OncoLinkRx.

How do chemotherapy drugs work?

The object of all chemotherapy drugs is to kill the cancerous cells and not harm the adjacent healthy cells. To that end, scientists tried to identify characteristics that are unique to cancer cells and are not found on normal tissue. A distinct cancer trait could serve as a potential target for a chemotherapy drugs and thereby fulfill the above goal. One feature that is truly unique for most cancer cells is that they grow at a rate faster than normal cells. Therefore targeting some aspect of the cell growth cycle seems reasonable. Fast growing cells would be affected the most and slow growing cells would be least disturbed. In fact, that is the basis for many chemotherapeutics. This seems obvious when considering the side effect profiles of most chemotherapy drugs. Hair follicles, skin, and the cells that line the gastrointestinal tract are some of the fastest growing cells in the human body, and therefore are most sensitive to the effects of chemotherapy. It is for this reason that patients may experience hair loss, diarrhea, and rashes.

The human body processes and excretes all drugs through either the liver or the kidneys. Therefore, when a patient has kidney or liver damage, giving chemotherapy becomes precarious. Administering the recommended amount of drug may prove to be too toxic in a patient unable to metabolize and excrete it. The pharmacokinetics for cancer patients are very complex and chemotherapy pharmacology is a subspecialty on its own. Unfortunately, kidney and liver damage often result due to cancer invasion, limiting the patient's chemotherapy options.

Pharmacokinetics is further complicated in the cancer patient, as they are often taking multiple medications, some of which have overlapping metabolic pathways and side effect profiles. An example of this difficult situation is in the brain cancer patient. Because brain tumors often present as seizures, many of these patients take anti-seizure medications. Anti-seizure medications are metabolized by the liver and affect the metabolism of many chemotherapy drugs. Dose adjustments are an absolute necessity to avoid toxicities or sub-therapeutic dosing.

The cell cycle

The cell cycle is broken up into four phases the G1, S, G2, and M phases. The G1 phase is the phase most active in protein synthesis. The cellular DNA at this phase is tightly coiled and is not actively being transcribed. Few chemotherapy agents are active at this phase of the cell cycle. By contrast, the S phase is the synthetic phase of the cell cycle. DNA replication is most active and many chemotherapeutic agents are most active in this phase. G2 represent a time when mostly RNA, but some protein, is actively produced. Mitosis, actual cell division, occurs during the M phase. There are two major classes of chemotherapy drugs that are most active during this phase of the cell cycle.

The remainder of this article includes a summary of the major classes of chemotherapy drugs.

Alkylating agents

Alkylating agents are the oldest class of anticancer drugs. Almost all of these drugs are active or latent nitrogen mustards. Nitrogen mustards are various poisonous compounds originally developed for military use. Alkylating agents all share a common mechanism of action but differ in their clinical activity. They attack the negatively charged sites on the DNA -- the oxygen, nitrogen, phosphorous and sulfur atoms. By binding to the DNA, replication, transcription and even base pairing are significantly altered. Alkylation of the DNA also leads to DNA strand breaks and DNA strand cross- linking. By altering DNA in this manner, cellular activity is effectively stopped and the cell will die. Chemotherapy drugs in this class are active in every stage of the cell cycle. As a consequence, this class of anticancer drugs is very powerful and is used in most every type of cancer both solid tumors and leukemia.

In general, prolonged use of these drugs will lead decreased sperm production, cessation of menstruation, and possibly cause permanent infertility. This class of chemotherapeutics should never be used in the first trimester of pregnancy as they are been shown to increase fetal malformations. Use in the second or third trimester does not seem to carry the same risk. All alkylating agents can cause secondary cancers although not all agents are equal in their carcinogenic potential. The most common secondary cancer is a leukemia (Acute Myeloid Leukemia) that can occur years after therapy.

Some of the more common alkylating agents include: Cyclophosphamide, Ifosphamide, Melphalan, Chlorambucil, BCNU, CCNU, Decarbazine, Procarbazine, Busulfan, and Thiotepa.


Antimetabolites

In 1948, Dr. Sidney Farber showed that a folic acid analog could induce remission in childhood leukemia. Approximately 10 out of the 16 patients treated demonstrated evidence of hematologic improvement. This experience provided the foundation for scientists to synthesize a number of other agents that either target naturally occurring compounds or inhibit key enzymatic reactions in their biochemical pathways. In general, all antimetabolites interfere with normal metabolic pathways, including those necessary for making new DNA. The most widely used antifolate in cancer therapy with activity against leukemia, lymphoma, breast cancer, head and neck cancer, sarcomas, colon cancer, bladder cancer and choriocarcinomas is Methotraxate. Methotraxate inhibits a crucial enzyme required for DNA synthesis and therefore exerts its effect on the S phase of the cell cycle.

Another widely used antimetabolite that thwarts DNA synthesis by interfering with the nucleotide (DNA components) production is 5-Fluorouracil. It too has a wide range of activity including colon cancer, breast cancer, head and neck cancer, pancreatic cancer, gastric cancer, anal cancer, esophageal cancer and hepatomas. A unique and interesting aspect of this drug is its toxicity profile. 5-Fluorouracil is metabolized by a naturally occurring enzyme called dihydropyrimidine dehydrogenase, DPD. There is a small population of people who may be deficient of this particular enzyme. Lacking DPD does not interfere with normal body biochemistry and thus the phenotype is silent. However, when these patients are challenged with this chemotherapy drug, they are unable to metabolize it and therefore get acute and sever toxicity. The most often seen toxicities include bone marrow suppression, severe GI toxicities, and neurotoxicities which may include seizures and even coma. It is important for the oncologist to recognize this early and provide the patient with Thymidine as an antidote. A drug called Capecitabine is an oral pro-5-Fluorouracil compound that has similar side effect potentials.

Other antimetabolites that inhibit DNA synthesis and DNA repair include: Cytarabine, Gemcitabine (Gemzar®), 6-mercaptopurine, 6-thioguanine, Fludarabine, and Cladribine.

Anthracyclines

Many of the currently effective anti-cancer drugs are from natural sources. The drug, daunorubicin was isolated from Streptomyces, a soil-dwelling fungus. Doxorubicin, another Anthracycline drug, was isolated from a mutated strain of the same fungus. Both of these drugs have a similar mechanism of action, but the latter is more effective in the treatment of carcinomas. This class of chemotherapeutics works by the formation of free oxygen radicals. These radicals result in DNA strand breaks and subsequent inhibition of DNA synthesis and function. Anthracyclines also inhibit the enzyme topoisomerase by forming a complex with the enzyme and DNA. Topoisomerases are a class of enzymes that serve to unwind the DNA double strand helix to allow for DNA repair, replication and transcription. This class of chemotherapeutics is also not cell cycle specific. The most important side effect of this group of drugs is cardiac toxicity. The same free radicals that serve to damage the DNA of the cancer cell may damage the cells of the heart muscle. Oncologists monitor heart function very carefully when patients are on these medications. Other commonly used anthracyclines include Idarubicin, Epirubicin and Mitoxantrone.

Antibiotic

Another small peptide isolated form the fungus Streptomyces verticullus is Bleomycin. Its mechanism of action is similar to that of the anthracyclines, in that free oxygen radicals are formed that result in DNA breaks leading to cancer cell death. This drug is rarely used by itself rather in conjunction to other chemotherapies. Bleomycin is an active agent in the regimen for testicular cancer as well as Hodgkin's lymphoma. The most concerning side effect of this drug is lung toxicities due to oxygen free radical formation.

Camptothecins

The drugs in this class of chemotherapeutics act by forming a complex with Topoisomerase and DNA resulting in the inhibition and function of this enzyme. The presence of Topoisomerase is required for on-going DNA synthesis. These drugs are used in many solid and liquid tumors and the side effect profile of this class of drugs is agent specific. Camptothecins include both irinotecan and topotecan. The parent compound, first identified in the late 1950's, is a naturally occurring alkaloid found in the bark and wood of the Chinese tree Camptotheca accuminata.

Etoposide, a chemotherapeutic that works by the same mechanism, is a natural product isolated from the mandrake plant and is not considered a camptothecin but rather an epipodophyllotoxin.

Vinca Alkaloids The leaves of a periwinkle plant, Vinca rosea, were used to make tea that reportedly improved diabetes. Early research showed that aqueous extract of this plant administered by injection into rats resulted in their death within a week. Further investigation showed that the rats die of sepsis due to bone marrow suppression caused by this extract. Isolation and chemical characterization lead to the currently used drugs: vincristine, vinblastine, and vinorelbine. These chemotherapeutics bind to the tubulin and lead to the disruption of the mitotic spindle apparatus. The disruption of mitosis implies that these drugs are active specifically during the M phase of the cell cycle. They have a wide application to many different malignancies and cause neurotoxicity as the most prominent and dose limiting side effect.

Taxanes

Another class of chemotherapeutics that are specific for the M phase of the cell cycle is the Taxanes. The taxanes include paclitaxel and docetaxel. They bind with high affinity to the microtubules and inhibit their normal function. This class of drugs has a broad range of clinical activity including breast cancer, lung cancer, head and neck cancer, ovarian cancer, bladder cancer, esophageal cancer, gastric cancer and prostate cancer. The most common side effect of these drugs is the lowering of the blood cells. These compounds were first isolated for the bark of the Pacific yew tree Taxus brevifolia in 1963. It was not until 1971 that paclitaxel was identified as the active component.

Platinums

Natural metal derivatives were also shown to have some activity in the fight against cancer. These agents work by cross-linking DNA subunits. (The cross linking can happen either between two strands or within one strand of DNA.) The resultant cross-link acts to inhibit DNA synthesis, transcription and function. The platinum compounds can act in any cell cycle. Cisplatin is used most often in lung cancer and testicular cancer. The most significant toxicity of cisplatin is kidney damage. Second-generation platinum, called carboplatin, has fewer kidney side effects, and at times may be an appropriate substitute for regiments containing cisplatinum. Oxaliplatin is a third-generation platinum that is active in colon cancer and has no renal toxicities, however, its major side effect is neuropathies.

Conclusion

There are other drugs now being used as effective therapies for malignancy. These include hormones for breast, prostate and endometrial cancers, monoclonal antibodies, immunotherapy with IL-2 and TNF alpha, and small molecule inhibitors. The process of drug discovery involves much time, effort and resources. New approaches are constantly being developed and modified. The process of testing a new agent in clinical trials begins with the discovery of new compounds, new ideas, new pathways, and new principles.

 
Prevention and Treatment of Oral Complications Before Chemotherapy and/or Radiation Therapy Begins

 

Finding and treating oral problems before anticancer therapy begins can prevent or lessen the severity of oral complications.

Oral complications in patients undergoing treatment for head and neck cancer may be reduced by aggressive prevention measures taken before treatment begins. This will get the mouth and teeth in the best possible condition to withstand treatment.

Preventive measures include the following:

  • Eating a well-balanced diet. Proper nutrition can help the body tolerate the stress of cancer treatment, maintain energy, fight infection, and rebuild tissue.
  • Learning how to care for the mouth and teeth during and after anticancer therapy. Good dental hygiene helps prevent cavities, mouth sores, and infections.
  • Having a complete oral health exam by a dentist familiar with the oral side effects of anticancer treatments.

The cancer care team should include the patient's dentist. It is important to choose a dentist familiar with the oral side effects of chemotherapy and/or radiation therapy. An evaluation of the patient's oral health at least a month before treatment begins usually provides enough time for the mouth to heal after dental work. The dentist will identify and treat teeth at risk for infection or decay, so the patient may avoid having invasive dental treatment during anticancer therapy. The dentist may also provide appropriate preventive care to lessen the severity of dry mouth, a common complication of radiation therapy to the head and neck.

A preventive oral health exam will check for the following:

  • Mouth sores or infections.
  • Tooth decay.
  • Gum disease.
  • Dentures that do not fit well.
  • Problems moving the jaw.
  • Problems with the salivary glands.

Patients undergoing high-dose chemotherapy, stem cell transplant, and/or radiation therapy need an oral care plan in place before treatment begins.

The goal of the oral care plan is to find and treat oral disease that may produce complications during treatment and to continue oral care throughout treatment and recovery. Different oral complications may occur during the different phases of transplantation. Steps can be taken ahead of time to prevent or lessen the severity of these side effects.

Ongoing oral care during radiation therapy will depend on the specific needs of the patient; the dose, locations, and duration of the radiation treatment; and the specific complications that occur.

It is important that patients who have head or neck cancer stop smoking.

Continued smoking slows recovery and increases the risk that the head or neck cancer will recur or that a second cancer will develop. (Refer to the PDQ summary on Smoking Cessation and Continued Risk in Cancer Patients for more information.)

 
Management of Oral Complications During and After Chemotherapy and/or Radiation Therapy

Routine Oral Care
Oral Mucositis
Infection
Bleeding
Dry Mouth
Tooth Decay
Taste Changes
Fatigue
Pain
Jaw Stiffness
Tissue and Bone Loss
Routine Oral Care

Continuing good dental hygiene during and after cancer treatment can reduce complications such as cavities, mouth sores, and infections. It is important to clean the mouth after eating. The following are guidelines for everyday oral care during chemotherapy and radiation therapy:

Tooth brushing

  • Brush teeth and gums with a soft bristle brush 2 to 3 times a day for 2 to 3 minutes.
  • Rinse the toothbrush in hot water every 15 to 30 seconds to soften the bristles, if needed.
  • If it is necessary to use a foam toothbrush, use it with an antibacterial rinse, when possible.
  • Allow the toothbrush to air dry between brushings.
  • Choose toothpaste with care:
    • Use a mild-tasting toothpaste; flavoring may irritate the mouth.
    • If toothpaste irritates the mouth, brush with a solution of 1 teaspoon of salt added to 4 cups (1 quart) of water.
    • Use a fluoride toothpaste.

Rinsing

  • Rinse the mouth 3 or 4 times while brushing.
  • Avoid rinses containing alcohol.
  • One of the following rinses made with salt and/or baking soda may be used:
    • 1 teaspoon of salt in 4 cups of water.
    • 1 teaspoon of baking soda in 1 cup (8 ounces) of water.
    • ½ teaspoon salt and 2 tablespoons baking soda in 4 cups of water.
  • An antibacterial rinse may be used 2 to 4 times a day for gum disease. Rinse for 1 to 2 minutes.
  • If dry mouth occurs, rinsing may not be enough to clean the teeth after a meal. Brushing and flossing may be needed.

Flossing

  • Floss gently once a day.

Lip care

  • Use lip care products to prevent drying and cracking.

Oral Mucositis

Mucositis is an inflammation of mucous membranes in the mouth.

The terms "oral mucositis" and "stomatitis" are often used in place of each other, but their meanings are different.

  • Mucositis is an inflammation of mucous membranes in the mouth. It usually appears as red, burn-like sores or as ulcer-like sores throughout the mouth.
  • Stomatitis is an inflammation of tissues in the mouth, such as the gums, tongue, roof and floor of the mouth, and tissues inside the lips and cheeks. It includes infections of mucous membranes.

Mucositis may be caused by either radiation therapy or chemotherapy. In patients receiving chemotherapy, mucositis will heal by itself, usually in 2 to 4 weeks when there is no infection. Mucositis caused by radiation therapy usually lasts 6 to 8 weeks, depending on the duration of treatment.

The following problems may occur:

  • Pain.
  • Infection.
  • Bleeding, in patients receiving chemotherapy. Patients undergoing radiation therapy usually do not have a bleeding risk.
  • Inability to breathe and eat normally.

Swishing ice chips in the mouth for 30 minutes may help prevent mucositis from developing in patients who are given fluorouracil.

Care of mucositis during chemotherapy and radiation therapy focuses on cleaning the mouth and relieving the symptoms.

Treatment of mucositis caused by either radiation therapy or chemotherapy is generally the same. After mucositis has developed, proper treatment depends on its severity and the patient's white blood cell count. The following are guidelines for treating mucositis during chemotherapy, stem cell transplantation, and radiation therapy:

Cleaning the mouth

  • Clean the teeth and mouth every 4 hours and at bedtime, more often if the mucositis becomes worse.

     
  • Use a soft bristle toothbrush.

     
  • Use water-soluble lubricating jelly to moisturize the mouth.

     
  • Use bland rinses or plain sterile water. Frequent rinsing removes particles and bacteria from the mouth, prevents crusting of sores, and moistens and soothes sore gums and the lining of the mouth. The following rinse may be used to neutralize acid and dissolve thick saliva:
    • ½ teaspoon salt and 2 tablespoons baking soda in 4 cups of water.



     

  • If crusting of sores occurs, the following rinse may be used:
    • Equal parts hydrogen peroxide and water or saltwater (1 teaspoon of salt in 4 cups of water).

    This should not be used for more than 2 days because it will keep mucositis from healing.

     

Relieving pain

  • Try topical medications for pain. Rinse the mouth before applying the medication onto the gums or lining of the mouth. Wipe mouth and teeth gently with wet gauze dipped in saltwater to remove particles.

     
  • Painkillers may provide relief when topical medications do not. Nonsteroidal anti-inflammatory drugs (NSAIDS, aspirin-type painkillers) should not be used by patients receiving chemotherapy because these patients have a bleeding risk.

     
  • Capsaicin, the active ingredient in hot peppers, may be used to increase a person's ability to tolerate pain. When capsaicin is put on inflamed tissues in the mouth, mucositis pain may decrease as the burning feeling from the capsaicin decreases. The side effects of capsaicin are not known.
     

Infection

Damage to the lining of the mouth and a weakened immune system make it easier for infection to occur.

Oral mucositis breaks down the lining of the mouth, allowing germs and viruses to get into the bloodstream. When the immune system is weakened by chemotherapy, even good bacteria in the mouth can cause infections, as can disease-causing organisms picked up from the hospital or other sources. As the white blood cell count gets lower, infections may occur more often and become more serious. Patients who have low white blood cell counts for a long time are more at risk of developing serious infections. Dry mouth, common during radiation therapy to the head and neck, may also raise the risk of infections in the mouth. Preventive dental care during chemotherapy and radiation therapy can reduce the risk of mouth, tooth, and gum infections.

The following types of infections may occur:

Bacterial infections

Treatment of bacterial infections in patients who have gum disease and receive high-dose chemotherapy may include the following:

  • Medicated and peroxide mouth rinses.
  • Brushing and flossing.
  • Wearing dentures as little as possible.

Bacterial infections in patients undergoing radiation therapy are usually treated with antibiotics.

Fungal infections

The mouth normally contains fungi that can exist on or in the body without causing any problems. An overgrowth of fungi, however, can be serious and requires treatment.

Antibiotics and steroid drugs are often used when a patient receiving chemotherapy has a low white blood cell count. These drugs change the balance of bacteria in the mouth, making it easier for a fungal overgrowth to occur. Fungal infections are common in patients treated with radiation therapy.

Drugs may be given to prevent fungal infections from occurring. Treatment of surface fungal infections in the mouth only may include mouthwashes and lozenges that contain antifungal drugs. These are used after removing dentures, brushing the teeth, and cleaning the mouth. An antibacterial rinse should be used on dentures and dental appliances and to rinse the mouth.

Deeper fungal infections, such as those in the esophagus or intestines, are treated with drugs taken by mouth or injection.

Viral infections

Patients receiving chemotherapy, especially those with weakened immune systems, are at risk of mild to serious viral infections. Finding and treating the infections early is important. Drugs may be used to prevent or treat viral infections.

Herpesvirus infections may recur in radiation therapy patients who have these infections.

Bleeding

Bleeding may occur during chemotherapy when anticancer drugs affect the ability of blood to clot.

Areas of gum disease may bleed on their own or when irritated by eating, brushing, or flossing. Bleeding may be mild (small red spots on the lips, soft palate, or bottom of the mouth) or severe, especially at the gumline and from ulcers in the mouth. When blood counts drop below certain levels, blood may ooze from the gums.

With close monitoring, most patients can safely brush and floss throughout the entire time of decreased blood counts.

Continuing regular oral care will help prevent infections that may further complicate bleeding problems. The dentist or doctor can provide guidance on how to treat bleeding and safely keep the mouth clean when blood counts are low.

Treatment for bleeding during chemotherapy may include the following:

  • Medications to reduce blood flow and help clots form.
  • Topical products that cover and seal bleeding areas.
  • Rinsing with a mixture of one part 3% hydrogen peroxide to 2 or 3 parts saltwater solution (1 teaspoon of salt in 4 cups of water) to help clean oral wounds. Rinsing must be done carefully so clots are not disturbed.

Dry Mouth

Dry mouth (xerostomia) occurs when the salivary glands produce too little saliva.

Saliva is needed for taste, swallowing, and speech. It helps prevent infection and tooth decay by neutralizing acid and cleaning the teeth and gums. Chemotherapy and radiation therapy can damage salivary glands, causing them to produce too little saliva. The mouth is less able to clean itself. Acid in the mouth is not neutralized, and minerals are lost from the teeth. Tooth decay and gum disease are more likely to develop. Symptoms of dry mouth include the following:

  • Thick, stringy saliva.
  • Increased thirst.
  • Changes in taste, swallowing, and speech.
  • A sore or burning feeling (especially on the tongue).
  • Cuts or cracks in the lips or at the corners of the mouth.
  • Changes in the surface of the tongue.
  • Difficulty wearing dentures.

Salivary glands usually return to normal after chemotherapy ends.

Dry mouth during chemotherapy is usually temporary. The salivary glands often recover 2 to 8 weeks after chemotherapy ends.

Salivary glands may not recover completely after radiation therapy ends.

Saliva production drops within 1 week after starting radiation therapy to the head and/or neck and continues to decrease as treatment continues. The severity of dry mouth depends on the dose of radiation and the number of glands irradiated. The salivary glands in the upper cheeks near the ears are more affected than other salivary glands.

Partial recovery of salivary glands may occur in the first year after radiation therapy, but recovery is usually not complete, especially if the salivary glands were directly irradiated. Salivary glands that were not irradiated may become more active to offset the loss of saliva from the destroyed glands.

Careful oral hygiene can help prevent mouth sores, gum disease, and tooth decay caused by dry mouth.

The following are guidelines for managing dry mouth:

  • Clean the mouth and teeth at least 4 times a day.
  • Floss once a day.
  • Use a fluoride toothpaste when brushing.
  • Apply fluoride gel once a day at bedtime, after cleaning the teeth.
  • Rinse 4 to 6 times a day with a solution of salt and baking soda (mix ½ teaspoon salt and ½ teaspoon baking soda in 1 cup of warm water). Avoid foods and liquids that contain a lot of sugar. Sip water to relieve mouth dryness.

A dentist can provide the following treatments:

  • Solutions to replace minerals in the teeth.
  • Rinses to fight infection in the mouth.
  • Saliva substitutes or medications to stimulate the salivary glands.
  • Fluoride treatments to prevent tooth decay.

Tooth Decay

Dry mouth and changes in the balance of oral bacteria increase the risk of tooth decay. Meticulous oral hygiene (as described in Routine Oral Care) and regular care by a dentist can help prevent cavities.

Taste Changes

Changes in taste are common during chemotherapy and radiation therapy.

Change in the sense of taste (dysgeusia) is a common side effect of both chemotherapy and head and/or neck radiation therapy. Foods may have no taste or may not taste as they did before therapy. These taste changes are caused by damage to the taste buds, dry mouth, infection, and/or dental problems. Chemotherapy patients may experience unpleasant taste related to the spread of the drug within the mouth. Radiation may cause a change in sweet, sour, bitter, and salty tastes.

In most patients receiving chemotherapy and in some patients undergoing radiation therapy, taste returns to normal a few months after therapy ends. For many radiation therapy patients, however, the change is permanent. In others, the taste buds may recover 6 to 8 weeks, or later, after radiation therapy ends. Zinc sulfate supplements may help with the recovery for some patients.

Taste changes can lead to a loss of appetite and malnutrition.

Unpleasant changes in the taste of food can cause a patient with cancer to lose the desire to eat. The patient's quality of life and nutritional well-being may be affected by loss of appetite. The following suggestions may help patients with cancer manage taste changes and meet nutritional needs:

  • Change the texture of food. Serving food chopped, ground, or blended can reduce the amount of time it needs to stay in the mouth before being swallowed.
  • Eat between-meal snacks to add calories and nutrients.
  • Choose foods high in calories and protein.
  • Take supplements that provide vitamins, minerals, and calories.

Nutritional counseling may be helpful during and after therapy.

Fatigue

Cancer patients who are undergoing high-dose chemotherapy and/or radiation therapy often experience fatigue (lack of energy) that is related to either the cancer or its treatment. Some patients may have difficulty sleeping. The patient may feel too tired to perform routine oral care, which may further increase the risk for mouth ulcers, infection, and pain. (Refer to the PDQ summary on Fatigue for more information.)

Pain

Certain anticancer drugs can cause nerve damage that may result in oral pain.

If an anticancer drug is causing the pain, stopping the drug usually stops the pain. Because there may be many causes of oral pain during cancer treatment, a careful diagnosis is important. This may include obtaining a medical history, performing physical and dental exams, and taking x-rays of the teeth.

Tooth sensitivity may occur in some patients weeks or months after chemotherapy has ended. Fluoride treatments and/or toothpaste for sensitive teeth may relieve the discomfort.

Pain in the teeth or jaw muscles may occur from tooth grinding or stress.

Pain in the teeth or jaw muscles may occur in patients who grind their teeth or clench their jaws, often because of stress or the inability to sleep. Treatment may include the following:

  • Muscle relaxers.
  • Drugs to treat anxiety.
  • Physical therapy (moist heat, massage, and stretching).
  • Mouthguards to wear while sleeping.

Jaw Stiffness

A long-term complication of radiation therapy is the growth of benign tumors in the skin and muscles. These tumors may make it difficult for the patient to move the mouth and jaw normally. Oral surgery may also affect jaw mobility. Management of jaw stiffness may include the following:

  • Physical therapy.
  • Oral appliances.
  • Pain treatments.
  • Medication.

Tissue and Bone Loss

Radiation therapy can cause tissue and bone in the treated area to waste away. When tissue death occurs, ulcers may form in the soft tissues of the mouth, grow in size, and cause pain or loss of feeling. Infection becomes a risk. As bone tissue is lost, fractures can occur. Preventive care can lessen the severity of tissue and bone loss.

Treatment of tissue and bone loss may include the following:

  • Eating a well-balanced diet.
  • Wearing removable dentures or appliances as little as possible.
  • Not smoking.
  • Not drinking alcohol.
  • Using topical antibiotics.
  • Using painkillers.
  • Undergoing surgery to remove dead bone or to reconstruct bones of the mouth and jaw.
  • Receiving hyperbaric oxygen therapy, a method of delivering oxygen under pressure to the surface of a wound to help it heal
 
Hopefully this website will help you.  You run across  something on this topic from friends or from the internet  If you would like us to enter the article on this page we can usually do so.
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