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Efficacy of neoadjuvant chemotherapy in male breast cancer compared with female breast cancer
Author(s) -
Leone José Pablo,
Hassett Michael J.,
Leone Julieta,
Tolaney Sara M.,
Vallejo Carlos T.,
Leone Bernardo A.,
Winer Eric P.,
Lin Nancy U.
Publication year - 2022
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.34448
Subject(s) - medicine , breast cancer , odds ratio , cancer , human epidermal growth factor receptor 2 , oncology , logistic regression , chemotherapy , male breast cancer , gynecology
Background Neoadjuvant chemotherapy (NAC) is standard for many females with breast cancer (FBC). The efficacy of NAC in male breast cancer (MaBC) is unclear. The aim of this study was to compare proportions of pathologic complete response (pCR) between MaBC and FBC by tumor subtype (TS). Methods MaBC and FBC treated with NAC between 2010 and 2016, with known TS, were evaluated from the National Cancer Database. Proportions of pCR (ypT0/Tis ypN0) were compared between sexes within TS by Fisher test. Multivariable logistic regression assessed the independent association of sex with pCR. Overall survival (OS) was estimated by Kaplan–Meier. Results A total of 385 MaBC and 68,065 FBC were included. Median time from initiation of NAC to surgery was 143 days in MaBC and 148 days in FBC. Proportions of pCR in MaBC and FBC by TS were: hormone receptor–positive/human epidermal growth factor receptor 2–negative (HR+/HER2–): 4.9% vs 9.7%, p = .01; HR+/HER2+: 16.1% vs 33.6%, p < .001; HR–/HER2+: 44.0% vs 53.2%, p = .42; and HR–/HER2–: 21.4% vs 32.1%, p = .18, respectively. FBC had twice the odds of pCR than MaBC (adjusted odds ratio, 2.0; 95% CI, 1.5–2.8; p < .001). Five‐year OS for MaBC with pCR vs not was 90% vs 64.7%; p = .02. Five‐year OS for FBC with pCR vs not was 91.9% vs 75.3%; p < .01. Conclusions Proportions and odds of pCR to NAC were numerically lower in MaBC compared with FBC for each TS and statistically significant for HR+/HER2– and HR+/HER2+. The independent association of sex with pCR was confirmed in multivariable analysis. pCR is prognostic in both MaBC and FBC.