четверг, 20 марта 2008 г.

Late treatment with letrozole can reduce breast cancer recurrence risk

Results of a study involving women originally in the placebo arm of an international trial of letrozole will appear in the Journal of Clinical Oncology and are receiving early online release.Who chose to begin letrozole treatment after the initial trial was halted, the risk that their cancer would recur was cut in halfpared with those who never received letrozole.Addition, the risk of metastasis was 60 percent lower with letrozole, and the chance that a new tumor would develop in the unaffected breast dropped more than 80 percent._See also:_ REFERENCE "It appears that estrogen-sensitive tumors remain hormone dependent and that patients' survival can be improved with careful use of aromatase inhibitors, even many years afterpleting tamoxifen treatment," says Paul E.MD, PhD, director of Breast Cancer Research at Massachusetts General Hospital Cancer Center, who led both the current study and the earlier investigation, called the MA."These results can be put into practice right away to improve the outlook for women treated for receptor-positive breast cancer.Is one of a class of drugs called aromatase inhibitors that suppress the production of estrogen, which stimulates the growth of breast tumors expressing the estrogen receptor.Most widely used estrogen-blocking drug is tamoxifen, but the benefits of tamoxifen treatment drop significantly after five years, while the drugs' side effects continue.The original MA.Conducted through the National Cancer Institute of Canada, was designed to test whether letrozole could reduce tumor recurrence and increase survival in breast cancer patients who hadpleted five years of tamoxifen treatment.Study was halted in October 2003 a year earlier than planned when interim data analysis showed that tumors of women taking letrozole were significantly less likely to recur.Final analysis of MA.In the September 7, 2005 Journal of the National Cancer Institute, confirmed that women taking letrozole had significantly better disease-free survival than those taking a placebo.Since women who received letrozole in the MA.Began taking the drug within a few months of stopping tamoxifen treatment, letrozole's current approval restricts the initiation of therapy to the first three months after tamoxifen discontinuation.In the placebo arm of the MA.Were offered the opportunity to begin letrozole treatment when that trial was halted, which gave investigators the opportunity to determine whether those women could also benefit from the drug.The current study analyzes data on more than 1,500 women from the placebo group who chose to take letrozole and about 800 who chose no further treatment.Three years after the MA.Was halted and letrozole offered, those who began letrozole therapy had only a 2 percent risk of tumor recurrence,pared with almost 5 percent in those choosing no treatment.Risk of death from breast cancer during that period was cut in half in those receiving letrozole.Also reduced the risk of metastasis by 61 percent and appeared to prevent development of a new tumor in the opposite breast by 82 percent.The research team notes that this study is limited by the fact that participants choose whether to take the drug themselves and were not randomly assigned.A randomized clinical trial would more conclusively determine the benefit of letrozole treatment for those who have been off tamoxifen for several months or years or even those who never took the drug the results of this study can help guide physicians and patients in deciding whether letrozole therapy would be appropriate.Patient who has previously taken tamoxifen should discuss these new results with her oncologist.Risk that hormone-dependent breast cancer will recur continues indefinitely, and our results imply that aromatase inhibition is effective whenever initiated," says Goss, a professor of Medicine at Harvard Medical School The current study was supported by grants from the Canadian Cancer Society, the National Cancer Institute of Canada, the U.National Cancer Institute and Pharmacia Corp.Pharmaceuticals, which markets letrozole under the brand name Femara, also supported and provided study medications for the initial MA.And the current study.Co-authors of the JCO study are James Ingle, MD, Mayo Clinic; Silvana Martino, DO, Angeles Clinic and Research Center; Nicholas Robert, MD, Inova Fairfax Hospital, Falls Church, Virginia; Hyman Muss, MD, University of Vermont; Martine Piccart, MD, Institut Jules Bordet, Brussels; Monica Castiglione, MD, University of Bern; Dongsheng Tu, PhD, Lois Shepherd, MD, Michael Palmer, MSc, and Joseph Pater, MD, National Cancer Institute of Canada Clinical Trials Group; Kathleen Pritchard, MD, Toronto-Sunnybrook Regional Cancer Centre; Robert Livingston, MD, University of Washington; Nancy Davidson, MD, Johns Hopkins Hospital; Larry Norton, MD, Memorial Sloan-Kettering Cancer Center; Edith Perez, MD, Mayo Clinic, Florida; Jeffrey Abrams, MD, National Cancer Institute; and David Cameron, MD, Western General Hospital, Edinburgh.From materials provided by , via , a service of AAAS_.Need to cite this story in your essay, paper, or report?One of the following formats: APA MLA RELATED STORIES (Oct.2003) A Canadian-led international clinical trial has found that post-menopausal survivors of early-stage breast cancer who took the drug letrozole afterpleting an initial five years of tamoxifen .> (Jul.2005) Researchers at Yale School of Medicine have discovered the breast cancer growth regulator sEGFR, which may be a useful tool in monitoring a patient's responsiveness to treatment with the drug .> (Apr.2006) Concerns about the use of letrozole, an easy-to-use and inexpensive drug for the treatment of infertility, appear to be unfounded, according to a major study.Study contradicts an earlier, much .> (Dec.2001) A new cancer drug called letrozole (trade name Femara(R)) worked better at shrinking breast cancer tumors than did the front-line breast cancer drug tamoxifen among a group of postmenopausal women .> (Sep.2005) A study published in the September 2005 issue of _Arthritis width: 130px; 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