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The Oncologist, Vol. 10, No. 1, 15-21, January 2005; doi:10.1634/theoncologist.10-1-15
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 How Rapidly Do Oncologists Respond to Clinical Trial Data?
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How Rapidly Do Oncologists Respond to Clinical Trial Data?

Aman Buzdara, Cynthia Macahiligb

a Department of Medical Oncology, University of Texas, MD Anderson Cancer Center, Houston, Texas, USA; b Market Certitude LLC, Morristown, New Jersey, USA

Correspondence: Aman Buzdar, M.D., Department of Medical Oncology, University of Texas, MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA. Telephone: 713-792-2817; Fax: 713-794-4385; e-mail: abuzdar{at}mdanderson.org

In the era of evidence-based medicine, convincing clinical trial data should influence clinical practice if disseminated in an appropriate manner. Here we discuss the influence of clinical trial results from the Arimidex, Tamoxifen Alone or in Combination trial on the usage of tamoxifen and anastrozole in the treatment of postmenopausal women with hormone receptor-positive early breast cancer. Data were derived from structured interviews with practicing medical oncologists over a period of 28 months. The overall use of hormonal therapy was high and increasing over the period studied. Significant increases in the use of anastrozole as adjuvant hormonal therapy were accompanied by significant decreases in the use of tamoxifen. This culminated in the use of anastrozole surpassing tamoxifen use by the end of the study period, accounting for over 50% of hormonal therapy use for postmenopausal early breast cancer. This study suggests that the dissemination of key clinical data, accompanied by professional commentary and regulatory actions, can rapidly influence the clinical practice of medical oncologists.

Key Words. Early breast cancer • Hormonal • Postmenopausal • Adjuvant • Clinical trial




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