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Randomized Controlled Trial
. 2008 Sep;111(2):365-72.
doi: 10.1007/s10549-007-9774-6. Epub 2007 Oct 6.

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

Affiliations
Randomized Controlled Trial

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

N Lynn Henry et al. Breast Cancer Res Treat. 2008 Sep.

Abstract

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.

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Figures

Fig. 1
Fig. 1
Distribution of rheumatology referrals over time. Light gray bars represent patients eligible for referral who did not qualify for referral at a given timepoint. Black bars represent patients eligible for referral who did qualify for referral at a given timepoint. Percentage at top of each bar represents percent of patients referred to rheumatology at each timepoint
Fig. 2
Fig. 2
Frequency of symptoms reported by patients referred to rheumatology (n = 38)

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