Kidney, Head and Neck Cancers & MDS

Revlimid is approved for certain types of myelodysplastic syndrome, and Sutent was approved for both advanced kidney cancer and gastrointestinal stromal tumor.

ELIZABETH WHITTINGTON
PUBLISHED: 1:00 AM, FRI MARCH 24, 2006
Talk about this article with other patients, caregivers, and advocates in the Gastrointestinal stromal tumor CURE discussion group.
After positive results in a phase III trial and a recommendation from the Food and Drug Administration’s Oncology Drugs Advisory Committee, Revlimid (lenalidomide) was approved in late 2005 for certain types of myelodysplastic syndromes (MDS), a variety of blood disorders that can cause low blood counts, including anemia, which require frequent blood transfusions.

Revlimid is especially effective in a quarter of MDS patients who carry a specific chromosome 5 deletion. Taken orally, Revlimid can cause many of these patients to no longer need blood transfusions, improving their quality of life. A phase III trial showed Revlimid, a derivative of Thalomid (thalidomide), allowed two thirds of patients to become transfusion-independent for more than a year. Though no trial has shown a risk of birth defects in patients taking Revlimid, the drug is currently only available through a restricted distribution program called RevAssist, which requires doctors and pharmacists to register in order to prescribe the drug. Women must have regular pregnancy tests, and both men and women must use contraceptives.

In addition to MDS, Revlimid has also shown activity in patients with relapsed multiple myeloma. The FDA is considering the drug for multiple myeloma and is expected to approve Revlimid for that indication in mid-2006. It is also being tested in metastatic melanoma and chronic lymphocytic leukemia. Common side effects of Revlimid include neutropenia, fatigue and diarrhea.

For more information, visit www.revlimid.com.

The FDA approved a new oral drug called Sutent (sunitinib) in January for both advanced kidney cancer as well as a rare type of sarcoma of the stomach called gastrointestinal stromal tumor (GIST). The approval made Sutent the first drug to be simultaneously approved for two cancers.

Sutent blocks the activity of multiple enzymes (called tyrosine kinases) that are involved in transmitting signals from the outside to the inside of the cancer cell. Sutent can block the development of new blood vessels (called angiogenesis), essentially starving the tumor of blood and nutrients (see “Picking Up Momentum for Treating Renal Cell Carcinoma,”). In phase II trials, Sutent shrank tumors by at least a third in up to 37 percent of advanced kidney cancer patients.

GIST is a rare tumor that occurs in the stomach and other parts of the digestive system. Fortunately, most GIST patients respond to Gleevec (imatinib), but over time, some patients become resistant to Gleevec and need an alternative treatment. When used against Gleevec-resistant GIST, Sutent had significant activity, prolonging time to tumor progression from six weeks to 27 weeks when compared with placebo. The most commonly reported side effects include fatigue, diarrhea and a rash on the hands and feet.

For more information on Sutent, go to www.sutent.com.

Talk about this article with other patients, caregivers, and advocates in the Gastrointestinal stromal tumor CURE discussion group.
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