The U.S. Food and Drug Administration recently
approved the anti-cancer drug Taxol (generic name paclitaxel) to treat early stage breast cancer that has spread to the lymph nodes under the
arm. The approval comes after a unanimous recommendation from the FDAs Oncologic
Drugs Advisory Committee (ODAC). In the largest adjuvant breast cancer study ever
conducted, the Cancer and Leukemia Group B (CALGB) (http://www-calgb.uchicago.edu/)
observed a 20% decrease in recurrent node-positive breast cancer and a reduced mortality
rate of 26% in 3000 patients who were given Taxol. Taxol has been approved to treat early
breast cancer in patients who have received doxorubicin-based chemotherapy.
First marketed in 1992, Taxol has also
been used to treat metastatic breast cancer (cancer that has spread beyond the breast and
lymph nodes under the arm), ovarian cancer, certain
types of lung cancer, and in some cases, Karposis sarcoma (Karposis sarcoma is
a cancer that begins as soft, brownish, or purple pimples on the feet and spreads through
the skin to the lymph nodes and abdominal organs). Since it is now estimated that more
than 180,000 women will be diagnosed with breast cancer each year in the United States,
researchers are focusing more and more on preventive and early-stage
treatment options. According to the ODAC, 40% of breast cancer patients are candidates for
adjuvant chemotherapy (drug therapy in addition to other treatment).
Adjuvant chemotherapy
is commonly used in early breast cancer patients soon after breast surgery (lumpectomy or mastectomy) in
hopes of completely eliminating the cancer. Adjuvant therapies (chemotherapy, hormone
treatment, radiation, etc.) are often used alone or in
conjunction with other breast cancer treatments to prevent cancer from spreading to other
parts of the body. In clinical trials, women who received Taxol after chemotherapy
consisting of doxorubicin plus cyclophosphamide had significantly higher breast cancer
survival rates compared to women who underwent the doxorubin/cyclophosphamide chemotherapy
alone.
Richard L. Schilsky, M.D. and professor
of medicine at the University of Chicago believes using Taxol to treat early breast cancer
will greatly improve a patients chances of living disease-free. In its 3000 patient
study, the CALGB reported that Taxol was well-tolerated by most women.
Common side effects to Taxol include:
- a reduced white blood cell count
(myelosuppression)
- hair loss (alopecia)
- numbness in the extremities (peripheral
neuropathy)
Other side effects of Taxol include:
- muscle or joint pain
(myalgia/arthralgia)
- diarrhea
- nausea
In addition to treating early breast
cancer, Taxol is used to effectively treat advanced stages of the disease. A recent study
published in the Journal of Clinical Oncology revealed that women with metastatic
breast cancer who were given Taxol with CMFP (cyclophosphamide, methotrexate,
5-fluorouracil and prednisone) combination chemotherapy have a 39% two year survival rate
compared to a 20% survival rate among women who received CMFP chemotherapy alone.
Women with breast cancer are encouraged
to discuss Taxol with their cancer treatment team.
Additional resources and
references
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