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We recommend an additional end point, invasive breast cancer-free survival, which includes all invasive disease-free survival events except second nonbreast primary cancers. This end point should be considered for trials in which the toxicities of agents are well-known and where the risk of second primary cancer is small. Additionally, we provide end point recommendations for local therapy trials, low-risk populations, noninferiority trials, and trials incorporating patient-reported outcomes.
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Sara M. Tolaney
Elizabeth Garrett‐Mayer
Julia White
Journal of Clinical Oncology
Harvard University
University of Toronto
University of North Carolina at Chapel Hill
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Tolaney et al. (Tue,) studied this question.
www.synapsesocial.com/papers/69daaff44a1e15904c835b14 — DOI: https://doi.org/10.1200/jco.20.03613