Guide To Nutrition In Multiple Myeloma – Part 2: Supplements

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Published: Sep 2, 2010 3:48 pm
Guide To Nutrition In Multiple Myeloma – Part 2: Supplements

This article is the second in a two-part series about nutrition for multiple myeloma patients. The first article provides an introduction to nutrition for cancer patients as well as tips for getting the right nutrition. This, the second article, describes sources and amounts of nutrients that are important for myeloma patients.

Taking nutritional supplements is common among multiple myeloma patients and other cancer patients. These supplements, including vitamins, minerals, and various plant compounds, may be important to keep the body healthy, aid in the treatment of myeloma, or to reduce negative side effects of treatment.

However, supplements, even those found naturally in foods, have the potential to interact poorly with chemotherapy or other treatments. Physicians typically agree that eating a balanced and nutritional diet is important, but they are often hesitant to recommend the use of certain supplements, since there may be little to no research to show that they are effective and safe in myeloma patients (see a related Beacon forum discussion). So, please discuss all supplements with your doctor before taking any.

If you and your doctor decide that certain supplements may be right for you, there are several important things to keep in mind. In general, supplements should be taken with food, unless otherwise indicated. If you are being treated with Velcade (bortezomib), avoid taking supplements on the days you receive Velcade, as they can diminish the efficacy of Velcade. If your doctor approves a supplement regimen, ask your doctor to provide specific instructions on when and how to take the supplements.

In order to help you decide which supplements you may want to discuss with your doctor, this article will provide for each nutrient: information on its potential purpose in multiple myeloma treatment, where to find it in your normal diet, and the suggested doses for myeloma patients.

Acetyl-L Carnitine

Some small studies suggest supplementing with acetyl-L carnitine, a nutrient normally made in sufficient amounts by the body, can help reduce the symptoms of peripheral neuropathy (nerve damage to arms and legs that is a common side effect of myeloma treatment). Acetyl-L carnitine may also protect heart cells from damage from Doxil (doxorubicin liposomal) treatment.

Acetyl-L carnitine is found in beef, pork, and milk. As a supplement for peripheral neuropathy, patients can try 500 milligrams twice a day with food. Up to 2 grams a day is safe, but over 5 grams a day can cause diarrhea, appetite changes, body odor, and rash.

Alpha Lipoic Acid

Alpha lipoic acid is an antioxidant that is commonly used in supportive therapy for peripheral neuropathy in people treated for multiple myeloma. It is an antioxidant that is normally made in the body, but people can also take extra alpha lipoic acid through supplements. Myeloma patients with peripheral neuropathy can take 300 milligrams to 1 gram daily, with 600 milligrams often recommended for up to four weeks.

Patients should be aware that one study done in myeloma cells in a lab found that alpha lipoic acid may reduce the effectiveness of Velcade treatment.

Calcium

People with multiple myeloma may take calcium along with vitamin D to help support their bones. However, bone breakdown during multiple myeloma also releases unhealthy amounts of calcium in the blood, so patients should consult their doctors before considering calcium supplements.

Curcumin

Curcumin, a compound found in the spice turmeric, may work to kill myeloma cells and prevent them from multiplying. For those who have the pre-cancer conditions monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma, curcumin may slow progression to active multiple myeloma, but this has not yet been supported by clinical research.

At the same time, patients should beware that curcumin can also suppress the immune system, which can be dangerous for people with multiple myeloma, smoldering multiple myeloma, or MGUS. For more information, please see the related Beacon news and discussion.

There is no standard established dose for curcumin in multiple myeloma. In the few small studies available on curcumin as a myeloma therapy, patients usually take about 4 grams daily spread out over many doses throughout the day. In India, where turmeric is popular in cooking, the average daily consumption is much less—60 milligrams to 200 milligrams through diet.

Enzymes

A mixture of the enzymes papain, trypsin, and chymotrypsin may weaken myeloma cells and increase the likelihood of responding to conventional chemotherapy. Anecdotal evidence suggests drinking papaya juice, which is rich in papain, may also be helpful in cancer therapy (see related Beacon news).

Eating papaya or drinking papaya juice generally poses little risk, though people who are pregnant, are allergic to kiwi fruits or figs, or have problems with blood clotting should avoid papain. Also, raw papain can irritate the skin.

There is little data on the effectiveness of this type of therapy or how much enzyme supplement to take for multiple myeloma. An ongoing Phase 3 trial is studying three daily doses of a product called Wobe Mugos E, which contains 100 milligrams of papain, 40 milligrams of trypsin, and 40 milligrams of chymotrypsin. Side effects of papain supplements, such as Wobe Mugos E, include throat and stomach irritation.

Fish Oils

Fish oils commonly contain plenty of omega-3 fatty acids, which may boost peripheral nerve health. For this reason doctors sometimes recommend them for peripheral neuropathy. Omega-3 fatty acids may also work against cancers by reducing inflammation.

Omega-3 fatty acids perform many important functions in the body and are an essential part of a healthy diet. Healthy patients are recommended to take 1.1 grams of omega-3 fatty acids a day for women and 1.6 grams a day for men. No recommendations specifically for myeloma patients were found. Patients should be careful not to take more than 3 grams a day without medical supervision because of an increased risk of bleeding.

The science on the effects of omega-3 fatty acids on multiple myeloma is still preliminary—two studies from the 1990s showed certain omega-3s kill myeloma cells in mice. For those interested in trying fish oils in a clinical trial, a trial is recruiting volunteers who have MGUS or smoldering multiple myeloma for a study on whether omega-3 supplements will delay or prevent the progression of these diseases to symptomatic multiple myeloma. The trial is starting patients on 1.25 milligrams three times a day, and the dosage will be increased for patients who can tolerate it.

Ginger

Ginger is a well-known home therapy for nausea. The latest science supports using ginger alongside prescribed nausea medication to reduce nausea from chemotherapy (see related Beacon news). The study showed that 0.5 gram to 1 gram of ginger daily for three days before chemotherapy and the first three days of chemotherapy significantly reduced nausea.

Glutamine

Supplements of the amino acid glutamine may help with several major side effects of high dose-chemotherapy and bone marrow transplantation. Small studies have shown it may reduce peripheral neuropathy, mouth sores and mouth ulcers, and infections.

Patients can take 15 grams of a pure L-glutamine powder twice daily for a total of 30 grams.

Green Tea

A compound found in green tea, called epigallocatechin-3-gallate (EGCG), may aid in killing myeloma cells and prevent myeloma cells from multiplying. However, it may also block the anti-cancer activity of Velcade, leading researchers to advise people with multiple myeloma undergoing Velcade therapy to avoid green tea products and EGCG supplements (see related Beacon news).

For people with MGUS or smoldering multiple myeloma, the compounds in green tea may slow down or prevent their pre-cancer conditions from progressing to multiple myeloma. Since most MGUS and smoldering myeloma patients are not actively treated, there is no worry of interference with chemotherapy. One Phase 2 clinical trial is studying the effects of a daily green tea extract on people with MGUS and smoldering myeloma. The trial is recruiting participants in Detroit.

Iron

Anemia (low red blood cell counts) is a symptom of multiple myeloma and is also a common side effect of many myeloma treatments. Iron supplements may help certain people with their anemia. Anemia is often treated with a prescription hormone called erythropoietin that stimulates red blood cell production. In severe cases, blood transfusions may be necessary.

For those whose anemia therapy would get a boost from iron, doctors may recommend an oral iron supplement or, if that is not enough, intravenous iron. In addition, patients can try including iron-rich foods in their diet such as dried beans, fortified cereal, beef, and eggs.

At the same time, people with multiple myeloma who get blood transfusions are at risk for having too much iron in their bodies, so iron supplements are not right for all myeloma patients. Doctors can tell patients how much iron is needed, depending on their condition.

Magnesium

Magnesium may help with peripheral neuropathy. It also helps regulate calcium levels and can help strengthen bone. Green leafy vegetables, almonds, cashews, and halibut are all good sources of this essential mineral.

People with multiple myeloma can also take 250 milligrams of magnesium twice daily through an over-the-counter supplement, or they might get a prescription for a daily 400-milligram supplement, depending on how much magnesium their doctors find in blood tests. Patients should beware that too much magnesium can cause diarrhea.

Potassium

Doctors may recommend potassium for people getting treated for multiple myeloma to help with peripheral neuropathy. Patients can get potassium from food sources such as sweet potatoes, bananas, citrus fruits, peas, red meat, and chicken, or their doctor may recommend potassium supplements.

There are no documented cases of people getting too much potassium from food, but supplements can cause hyperkalemia, a dangerous condition than can lead to sudden cardiac arrest. Since the kidneys work to remove extra potassium from the body, people with multiple myeloma, which often reduces kidney function, might be especially vulnerable. Multiple myeloma patients should be especially careful to take potassium supplements only under direction from their doctors.

Resveratrol

Resveratrol, a compound abundant in grape skins, may kill myeloma cells, prevent myeloma cells from multiplying, and enhance the effects of some common chemotherapy drugs (see related Beacon news).

Those interested in including more resveratrol in their diet can enjoy grapes, purple grape juice, red wine, peanuts, blueberries, and cranberries.

There are also many resveratrol supplements available on the market. However, because there have not been any completed clinical trials on resveratrol in multiple myeloma therapy, there is no established dosage. A Phase 2 clinical trial was studying the effects of 5 grams daily of a formulation of resveratrol in multiple myeloma patients. However, the trial was suspended earlier this year after several patients developed kidney failure (see related Beacon news).

Vitamin B

B vitamins, including vitamin B-1 (thiamine), vitamin B-2 (riboflavin), vitamin B-6, vitamin B-12, and folic acid, are important for the formation of red blood cells, enhance the immune and nervous systems, and more. People with multiple myeloma often have low red blood cells counts and can suffer from peripheral neuropathy, so getting enough B vitamins may be especially important for those with multiple myeloma.

Good food sources of B vitamins include fortified breakfast cereal; other fortified grain products; animal products such as fish, poultry, meat, and dairy; vegetables such as carrots, peas, and leafy greens; fruits such as avocadoes, grapes, and dates; and beans.

Vitamin B-1 and vitamin B-12 are so common in foods, people rarely need to take supplements for them. For the other B vitamins, supplements commonly come in a B-vitamin complex formula that includes many or all of the B vitamins in one pill.

Recommended amounts for multiple myeloma patients with peripheral neuropathy include 50 milligrams of vitamin B-6 daily (but not more than 100 milligrams a day) and 1 milligram of folic acid daily.

Vitamin C

As an antioxidant, vitamin C helps protect cells from environmental damage that may lead to cancer. It also functions in protecting the immune system. The best protective benefits seem to result from obtaining vitamin C through fruits and vegetables, but the vitamin is still one of the most popular supplements for people with cancer.

Myeloma patients who are interested in vitamin C supplements should be aware that taking antioxidants on the same day as Velcade treatment reduces Velcade’s therapeutic effects (see related Beacon news). However, patients can still enjoy fruits and vegetables that are naturally high in vitamin C, such as red peppers, citrus fruits, kiwi, and broccoli.

Vitamin D

Vitamin D works with calcium to build bone, and recent research suggests it might be important in reducing some signs and symptoms of multiple myeloma. Supplements may help people with multiple myeloma deal with chronic bone pain, weakness, fatigue, and peripheral neuropathy. Meanwhile, vitamin D deficiency may be associated with poorer multiple myeloma prognoses (see related Beacon news).

Patients should aim to get 800 international units (IU) to 1,200 IU of vitamin D daily. Getting out in the sun every day for 15 minutes can go a long way toward keeping vitamin D levels up. Including fortified cereal and fortified milk, cheese, and other milk products in the diet can also prove beneficial. For those who cannot eat or drink dairy products, most alternatives, such as soy milk, rice milk, and almond milk, are fortified as much as cow’s milk. Vitamin D is also present naturally in fatty fish, such as salmon or tuna.

Many people do not get enough vitamin D through sun exposure and their diet, however. A daily supplement with 400 IU to 800 IU of vitamin D2 (ergocalciferol) or D3 (cholecalciferol) can help.

Vitamin E

For those suffering from peripheral neuropathy, vitamin E supplements may help. This antioxidant vitamin may protect nerves during therapy, especially with Velcade or thalidomide.

Additionally, Vitamin E may help heal mouth sores caused by chemotherapy. In a 2003 entry, multiple myeloma blogger Jon Siegel wrote about applying the contents of a vitamin E capsule to his mouth sores. He found he had “a relatively easy time of it compared to other folks” who had gone through chemotherapy.

For food sources of vitamin E, look to almonds, sunflower seeds and oil, peanut butter, and safflower oil. If taking a supplement, 400 IU daily is recommended.

For more information about nutrition for myeloma patients, see Part 1 in the series.  Feel free to post as a comment any recommendations your physicians made about these or additional supplements, and please remember to always consult with your doctors before taking any new supplements.

https://myelomabeacon.org/resources/2008/10/15/velcade/
Photo by bradley j on Flickr -- some rights reserved.
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13 Comments »

  • Marla Kressal said:

    My husband has Waldenstrom M. Lymphoma. He is being treated with Velcade. I was searching the web for an article that discusses food and vitamin supplement interaction with Velcade. I was having no luck (other than green tea should not be taken) until I found your website. I am especially interested in the papaya fruit and leaves, I make my husband papyaya shakes to raise his platelets. Glad to know it does not interfere with Velcade. Thank you for this informative page. I will bookmark it for future reference, very helpful. Sincerely, Marla Kressal.

  • John Andersen said:

    Hi Everyone,
    I went through chemo in 2010 and u8sed to eat RAW GARLIC sandwiches after treatments and most of the bad feelings from chemo, went away. I would slice up about 4 or 5 large cloves, use heavy whole wheat bread, lather both slices with butter, press the sliced garlic into the butter on one slice and put the two pieces of bread together and chow down. Im would also have a glass of cold water available to wash down the garlic as some garlic is really HOT and SPICY, and you need to get it into your stomach. Chew it good.
    Sometimes there is some suffering going on with really spicy garlic, but it is worth it to avoid the terrible feelings from the Chemo. It really works.
    Then I read that butter is to be cut way back or avoided with cancer. So, I began saturating the bread with extra Virgin olive oil,
    (the GOOD stuff, that is the color of "Olive Drab", do not use gold colored olive oil) The oil/butter really helps in combatting the heavy duty garlic TASTE of raw. If there is no olive oil around, I chew a large bite quickly and not breathe, so I don't taste it, and then I wash it down with cold water.
    What I am trying to do here is chew the garlic quickly andget it into my stomach with the water. If you do it on an empty stomach you may vomit, some garlic is too much! Experiment with low dose garlic sandwiches and work your way up. A garlic sandwich before bed is a way of waking up with some energy. Who cares about the odor!!! You will feel better. After awhile the odor goes down. Try some italian dishes but always eat the garlic raw. There are nutrients and enzymes that get destroyed by the heat of cooking. RAW GARLIC IS THE BEST !!!
    It has never failed me.

  • maria eugenia marin said:

    Necesito algunas sugerencias para AUMENTAR DE PESO, Tengo mieloma multiple desde el 2003 y estoy en recaida. Actualmente estoy tomando REVLIMID 10 mg diarios Y DEXAMETOZONA, 20 mg por semana Tengo muchos calambres..

    Translation: I need some suggestions for gaining weight. I have had multiple myeloma since 2003 and am in relapse. I am currently taking 10 mg Revlimid daily and 20 mg dexamethasone weekly. I have many cramps.

  • Joan Hamilton, said:

    For Maria. Try Carnation Instant Breakfast VHC. It is hard to find but you can find it on the internet, and some drug stores can order it for you. My husband has MM, he lost so much weight and he was and still is using Boost with a handful of Walnuts, and a scoop of ice cream, blended really well. But if he starts loosing weight again, we are going to try the Carnation Instant Breakfast VHC. One of the girls at the hospital told me about her husband who had to have a liver transplant and he lived on it for 6 mo. now has recovered but still drinks it every day, as a treat.

  • Gary said:

    Thanks for the helpful information! I'm in mile 1 and trying to understand why some folks don't make it and why some do. Perhaps it's their nutrition, perhaps fate.

  • Kathy said:

    My husband was diagnosed with Multiple Myeloma this past week. I am looking for many ways to help him out. He will begin chemo next week. I'm very overwhelmed at this time.

  • Helena said:

    Hi Kathy! Yes, it is overwhelming. In my experience, it does take time for the initial shock of the diagnosis to wear off, but it does wear off in its own time.
    My husband was diagnosed with multiple myeloma back in August 2008. After the initial shock wore off, (which in my case took months), I was able to follow my instinct and become matter-of-fact about his illness, in other words, my fears receded and I just went with it and supported him every way I could. We are going through this together and make the most of life, even with its limitations. My husband cannot walk very far, but enjoys eating out, playing bridge, visiting family, etc.,
    I still maintain my own hobbies - as someone said - "the jug has to be filled up again"!
    The best advice I got was to take things one day at a time.
    You have my very best wishes.

  • Dan D said:

    Hi Kathy

    It is overwhelming. The first day is one of isolation and sadness, where it feels like a glass window separates you from everything joyful and the excitement of future dreams and hopes. An incurable cancer will do that. And the assurance that hey, you could get hit by a car tomorrow, is no comfort. As one of the bloggers has pointed out, there is a difference between someone pointing a gun at your head versus known that bullet has been discharged and is coming at you.

    However -- this shock eventually transitions – for me -- into a combination of resolution, determination, and stubbornness fueled by need to understand everything about this disease. With this came the recognition that this cancer is highly individualized, and for many people, grows very slowly and does not readily metastasize. This does provide real comfort.

    I say all this, because I do wonder why your husband is starting treatment less than a week after being diagnosed. Was his diagnosis linked perhaps to a catastrophic event -- such as a pathological fracture or a transfusion?

    Please know that I am not an oncologist – and do not pretend to be one. I am just wondering. I am still struggling with when to begin treatment – my only symptom is mild anemia – and what that treatment will be.

  • Dan D said:

    To Kathy:

    Yeesh - sorry: I just noticed that your post is four months old. I was looking at the date of the initial response.

  • Terryl1 said:

    Hi Dan D.,

    What you wrote is actually pretty poignant and on target and encapsulates how I felt in August, 2011 when I first heard the %$#*&@! word myeloma. I also like your other posts and your conservative approach to myeloma. I hope to just keep smoldering along and I am also happy to see the start soon of the vaccine trail with Oncopep. I called about it and was told it would be at Mass General in Boston which is assocaited with Dana Farber. Terry L. from New Jersey

  • Dan D said:

    Hi Terry L

    Hi Terry. Thanks for your kind words.

    Of course, my views must be taken with a grain of salt, as I am not a doctor -- at least not the medical kind. I still plan to collect stem cells if I require treatment, and yes -- if absolutely necessary, I would not exclude a transplant down the road. But like you, I hope not to be at those crossroads for a while -- yet you never know!

    So keep on smoldering: And don't play with matches!

  • Terryl1 said:

    Thanks Dan D.,

    Call Mass General if you get a chance. The myeloma research nurse, Ms. Renaudie, was wonderful. She'll fill you in on the proposed trial with the peptides vaccine. Cheers!

  • Louise said:

    Hi,
    Not sure if this website is only for the USA but I'm looking for a complementary therapist in the UK who can advise on diet and nutritional supplements specifically for myeloma. I realise you can't 'recommend' as such, but I'd love to hear from anyone who's had a good experience with someone of this sort.
    Thanks a lot,
    Louise