Prospective characterization of musculoskeletal symptoms in early stage breast cancer patients treated with aromatase inhibitors

Springer Science and Business Media LLC - Tập 111 - Trang 365-372 - 2007
N. Lynn Henry1, Jon T. Giles2, Dennis Ang3, Monika Mohan4, Dina Dadabhoy4, Jason Robarge, Jill Hayden1, Suzanne Lemler3, Karineh Shahverdi5, Penny Powers5, Lang Li3, David Flockhart3, Vered Stearns5, Daniel F. Hayes1, Anna Maria Storniolo3, Daniel J. Clauw4
1Breast Oncology Program, University of Michigan Comprehensive Cancer Center, Ann Arbor, USA
2Division of Rheumatology, Johns Hopkins University, Baltimore, USA
3Department of Medicine, Indiana University School of Medicine, Indianapolis, USA
4Division of Rheumatology, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, USA
5Breast Cancer Program, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, USA

Tóm tắt

Purpose Aromatase inhibitors (AIs) are increasingly used as adjuvant treatment of postmenopausal women with hormone receptor-positive breast cancer. AIs are commonly associated with musculoskeletal symptoms. The primary objective of this study was to describe the musculoskeletal symptoms that developed in the first 100 subjects enrolled who had at least 6 months follow-up. Methods Women with early stage hormone receptor-positive breast cancer were recruited into a multicenter randomized clinical trial to study the pharmacogenomics of two AIs, exemestane, and letrozole. Patients completed the Health Assessment Questionnaire (HAQ) and Visual Analog Scale (VAS) at baseline, 1, 3, 6, and 12 months to assess changes in function and pain, respectively. Patients were referred for evaluation by a rheumatologist if their HAQ and/or VAS scores exceeded a predefined threshold. Results Forty-four of 97 eligible patients (45.4%) met criteria for rheumatologic referral. Three patients were ineligible because of elevated baseline HAQ (2) and failure to initiate AI therapy (1). No baseline characteristics were significantly associated with referral. Median time to onset of symptoms was 1.6 months (range 0.4–10 months). Clinical and laboratory evaluation of patients evaluated by rheumatology suggested that the majority developed either non-inflammatory musculoskeletal symptoms or inflammation localized to tenosynovial structures. Thirteen patients discontinued AI therapy because of musculoskeletal toxicity after a median 6.1 months (range 2.2–13 months). Conclusions Musculoskeletal side effects were common in AI-treated patients, resulting in therapy discontinuation in more than 10% of patients. There are no identifiable pre-therapy indicators of risk, and the etiology remains elusive.

Tài liệu tham khảo

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