Adjuvant ovarian function suppression and cognitive function in women with breast cancer
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Regan, Meredith M.
Ribi, Karin
Francis, Prudence A.
Puglisi, Fabio
Bellet, Meritxell
Spazzapan, Simon
Karlsson, Per
Budman, Daniel R.
Zaman, Khalil
Abdi, Ehtesham
Domchek, Susan M.
Feng, Yang
Price, Karen N.
Coates, Alan S.
Gelber, Richard D.
Maruff, Paul
Boyle, Frances M.
Forbes, John F.
Ahles, Tim
Fleming, Gini F.
Bernhard, Jurg
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Abstract
Background: To examine the effect on cognitive function of adjuvant ovarian function suppression (OFS) for breast cancer.
Methods: The Suppression of Ovarian Function (SOFT) trial randomised premenopausal women with hormone receptor-positive breast cancer to 5 years adjuvant endocrine therapy with tamoxifen+OFS, exemestane+OFS or tamoxifen alone. The Co-SOFT substudy assessed objective cognitive function and patient reported outcomes at randomisation (T0), and 1 year later (T1); the primary endpoint was change in global cognitive function, measured by the composite objective cognitive function score. Data were compared for the pooled tamoxifen+OFS and exemestane+OFS groups vs the tamoxifen alone group using the Wilcoxon rank-sum test.
Results: Of 86 participants, 74 underwent both T0 and T1 cognitive testing; 54 randomised to OFS+ either tamoxifen (28) or exemestane (26) and 20 randomised to tamoxifen alone. There was no significant difference in the changes in the composite cognitive function scores between the OFS+ tamoxifen or exemestane groups and the tamoxifen group (mean±s.d., −0.21±0.92 vs −0.04±0.49, respectively, P=0.71, effect size=−0.20), regardless of prior chemotherapy status, and adjusting for baseline characteristics.
Conclusions: The Co-SOFT study, although limited by small samples size, provides no evidence that adding OFS to adjuvant oral endocrine therapy substantially affects global cognitive function.
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British Journal of Cancer
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114
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Oncology and carcinogenesis
Oncology and carcinogenesis not elsewhere classified
Health services and systems
Public health