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ASCO Endorses Use of AIs

Posted 7/16/2010

Posted in

This is a report from Reuters about a new statement from ASCO (Association of Clinical Oncology) re the use of AIs as part of the treatment for post-menopausal women with hormone receptor breast cancers. Frankly, this feels like old news to me, and I am not sure why it is being heralded as a change in recommended standards of care. There continues to be uncertainty re the optimal duration of such treatments ( ? five years. ? 10 years, ? even longer), but I would assume that longer follow up on a number of trials will help answer that question.

ASCO endorses aromatase inhibitors for hormonesensitive

breast cancer

JULY 12, 2010

NEW YORK (Reuters Health) - Updated guidelines from the American Society of Clinical Oncology (ASCO) recommend that postmenopausal women with hormone receptor-positive breast cancer should receive aromatase inhibitor therapy at some point in their course of treatment.

Just one year ago, in a practice guideline update published in July 2009, ASCO said it could not recommend use of aromatase inhibitors outside of a clinical trial.

But based on newer data, an expert panel -- co-chaired by Dr. Harold J. Burstein from the Dana-Farber Cancer Institute, Boston and Dr. Jennifer J. Griggs at the University of Michigan in Ann Arbor - has come to a different conclusion. The panel conducted a systematic review of recent evidence on adjuvant endocrine therapy for postmenopausal hormone receptor-positive breast cancer, focusing on 12 major trials.

"An adjuvant treatment strategy incorporating an aromatase inhibitor (AI) as primary (initial endocrine therapy), sequential (using both tamoxifen and an AI in either order), or extended (AI after 5 years of tamoxifen) therapy reduces the risk of breast cancer recurrence compared with 5 years of tamoxifen alone," the panel concludes in its report in the Journal of Clinical Oncology released online July 12.

But while the guidelines recommend adjuvant AI therapy at some point, "the optimal timing and duration of AI treatment remain unresolved; it is unclear whether sequential treatment strategies yield advantages overmonotherapy with AIs."

An ASCO press release also highlighted several other recommendations made by the committee:

--Tamoxifen should be given to all premenopausal and perimenopausal women; AIs are only effective in postmenopausal women. Women who are pre- or peri-menopausal at the time of diagnosis should receive 5 years of tamoxifen.

--There are no clinically important differences in effectiveness among the three commercially available AIs (anastrozole, letrozole, and exemestane).

--As tamoxifen is a selective estrogen receptor modulator while AIs deplete the production of estrogen in postmenopausal women, aromatase inhibitors may reduce the chance of blood clots and uterine cancer but may increase the risk of osteoporosis and fractures.

"The Panel emphasized the importance of discussing side effects of these drugs with patients, to help patients better understand and choose between the treatments and do all we can to maximize compliance with these important therapies," said Dr. Griggs in the ASCO press release.

The clinical practice guideline and other clinical tools and resources are available atwww.asco.org/guidelines/endocrinebreast.

ASCO has also developed a corresponding patient guide available on its patient website, www.cancer.net.

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