TY - JOUR
T1 - Pathologic complete response after neoadjuvant chemotherapy in HER2-overexpressing breast cancer according to hormonal receptor status
AU - Tanioka, Maki
AU - Sasaki, Masaoki
AU - Shimomura, Akihiko
AU - Fujishima, Makoto
AU - Doi, Mihoko
AU - Matsuura, Kazuo
AU - Sakuma, Toshiko
AU - Yoshimura, Kenichi
AU - Saeki, Toshiaki
AU - Ohara, Masahiro
AU - Tsurutani, Junji
AU - Watatani, Masahiro
AU - Takano, Toshimi
AU - Kawabata, Hidetaka
AU - Mukai, Hirofumi
AU - Naito, Yoichi
AU - Hirokaga, Koichi
AU - Takao, Shintaro
AU - Minami, Hironobu
PY - 2014/8
Y1 - 2014/8
N2 - Objective: For patients with HER2-positive breast cancer, the prognostic impact of pathologic complete response (pCR) after neoadjuvant chemotherapy (NAC) is unclear when stratified by hormonal receptor (HR) status; however, the impact of pCR on survival when stratified by hormonal receptor (HR) status is uncertain. Patients and methods: This multicenter retrospective study investigated the predictors of pCR and its prognostic value in Japanese patients 366 HER2-positive breast cancer who received NAC. pCR was defined as no invasive residual tumor in the breast or axilla. Results: Median follow-up was 55 months. Multivariate analysis revealed that HR status (OR, 0.37; p<0.001) was one of the independent predictors of pCR. Five-year recurrence-free survival was higher in HR-negative patients with pCR (93%) than in those without pCR (68%), and pCR was independently prognostic (hazard ratio, 0.32; p=0.005). However, 5-year recurrence-free survival was not different between HR-positive patients with pCR (94%) and those without pCR (84%), and pCR was not significantly prognostic (hazard ratio, 0.53; p=0.39). In addition, 5-year overall survivals were high and similar (97% in pCR, 94% in non-pCR). Among 204 patients treated with neoadjuvant trastuzumab, pCR was not significantly prognostic in the HR-positive group (hazard ratio, 0.63; p=0.56). Conclusion: Our study suggested that the HER2-positive HR-positive patients had a good prognosis despite the lower achievement rate of pCR, whose prognostic impact was smaller than that in the HER2-positive HR-negative patients. The treatment strategy for HER2-positive breast cancer can be stratified by HR status.
AB - Objective: For patients with HER2-positive breast cancer, the prognostic impact of pathologic complete response (pCR) after neoadjuvant chemotherapy (NAC) is unclear when stratified by hormonal receptor (HR) status; however, the impact of pCR on survival when stratified by hormonal receptor (HR) status is uncertain. Patients and methods: This multicenter retrospective study investigated the predictors of pCR and its prognostic value in Japanese patients 366 HER2-positive breast cancer who received NAC. pCR was defined as no invasive residual tumor in the breast or axilla. Results: Median follow-up was 55 months. Multivariate analysis revealed that HR status (OR, 0.37; p<0.001) was one of the independent predictors of pCR. Five-year recurrence-free survival was higher in HR-negative patients with pCR (93%) than in those without pCR (68%), and pCR was independently prognostic (hazard ratio, 0.32; p=0.005). However, 5-year recurrence-free survival was not different between HR-positive patients with pCR (94%) and those without pCR (84%), and pCR was not significantly prognostic (hazard ratio, 0.53; p=0.39). In addition, 5-year overall survivals were high and similar (97% in pCR, 94% in non-pCR). Among 204 patients treated with neoadjuvant trastuzumab, pCR was not significantly prognostic in the HR-positive group (hazard ratio, 0.63; p=0.56). Conclusion: Our study suggested that the HER2-positive HR-positive patients had a good prognosis despite the lower achievement rate of pCR, whose prognostic impact was smaller than that in the HER2-positive HR-negative patients. The treatment strategy for HER2-positive breast cancer can be stratified by HR status.
KW - Breast cancer
KW - HER2
KW - Hormonal receptor
KW - Neoadjuvant chemotherapy
KW - Pathologic complete response
KW - Trastuzumab
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U2 - 10.1016/j.breast.2014.03.008
DO - 10.1016/j.breast.2014.03.008
M3 - Article
C2 - 24742606
AN - SCOPUS:84902551324
SN - 0960-9776
VL - 23
SP - 466
EP - 472
JO - Breast
JF - Breast
IS - 4
ER -