TY - JOUR
T1 - Pertuzumab retreatment for HER2-positive advanced breast cancer
T2 - A randomized, open-label phase III study (PRECIOUS)
AU - Yamamoto, Yutaka
AU - Iwata, Hiroji
AU - Taira, Naruto
AU - Masuda, Norikazu
AU - Takahashi, Masato
AU - Yoshinami, Tetsuhiro
AU - Ueno, Takayuki
AU - Toyama, Tatsuya
AU - Yamanaka, Takashi
AU - Takano, Toshimi
AU - Kashiwaba, Masahiro
AU - Tsugawa, Koichiro
AU - Hasegawa, Yoshie
AU - Tamura, Kenji
AU - Tada, Hiroshi
AU - Hara, Fumikata
AU - Fujisawa, Tomomi
AU - Niikura, Naoki
AU - Saji, Shigehira
AU - Morita, Satoshi
AU - Toi, Masakazu
AU - Ohno, Shinji
N1 - Funding Information:
Y.Y. receives lecture fees, honoraria, or other fees from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., and Pfizer Japan Inc., research funds from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Daiichi‐Sankyo Co., Ltd., and MSD K.K., and scholarship endowments from Chugai Pharmaceutical Co., Ltd. and Kyowa Kirin Co. Ltd. H.I. receives research funds from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Daiichi‐Sankyo Co., Ltd., Eli Lilly and Company, and MSD K.K. N.M. receives lecture fees, honoraria, or other fees from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Eisai Co. Ltd., Eli Lilly and Company, and Pfizer Japan Inc., research funds from AstraZeneca K.K., Chugai Pharmaceutical Co. Ltd., Daiichi‐Sankyo Co. Ltd., Eisai Co., Ltd., Eli Lilly and Company, Kyowa Kirin Co. Ltd., MSD K.K., Novartis Pharma K.K., Pfizer Japan Inc., and Sanofi K.K. (contract with the facility), and is a member of the editorial board of . M.T. (Takahashi) receives lecture fees, honoraria, or other fees from AstraZeneca K.K., Eisai Co. Ltd., Eli Lilly and Company, and Pfizer Japan Inc., and scholarship endowments from Kyowa Kirin Co., Ltd. and Taiho Pharmaceutical Co., Ltd. T.Y. (Yoshinami) receives lecture fees, honoraria, or other fees from Chugai Pharmaceutical Co., Ltd., Kyowa Kirin Co. Ltd., and Pfizer Japan Inc. T.U. receives lecture fees, honoraria, or other fees from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Eisai Co. Ltd., and Novartis Pharma K.K. T.T. (Toyama) receives lecture fees, honoraria, or other fees from Pfizer Japan Inc., and research funds from Chugai Pharmaceutical Co., Ltd. and Eisai Co. Ltd. T.T. (Takano) receives lecture fees, honoraria, or other fees from Chugai Pharmaceutical Co., Ltd., Celltrion Healthcare Japan Co., Daiichi‐Sankyo Co. Ltd., Eisai Co. Ltd., and Eli Lilly and Company. K.T. receives lecture fees, honoraria, or other fees from Chugai Pharmaceutical Co., Ltd. and Daiichi‐Sankyo Co. Ltd., research funds from Daiichi‐Sankyo Co. Ltd., Eli Lilly and Company, and Pfizer Japan Inc. F.H. receives lecture fees, honoraria, or other fees from Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., Eli Lilly and Company, Kyowa Kirin Co., Ltd., and Pfizer Japan Inc. N.N. receives lecture fees, honoraria, or other fees from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Daiichi‐Sankyo Co., Ltd., Eisai Co., Ltd., Eli Lilly and Company, and Pfizer Japan Inc., research funds from Chugai Pharmaceutical Co., Ltd., Daiichi‐Sankyo Co., Ltd., Eisai Co., Ltd., Nippon Kayaku Co., Ltd., and Pfizer Japan Inc., and is a member of the editorial board of . S.S. receives lecture fees, honoraria, or other fees from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Daiichi‐Sankyo Co., Ltd., Eisai Co., Ltd., Eli Lilly and Company, Kyowa Kirin Co., Ltd., and Pfizer Japan Inc., research funds from Chugai Pharmaceutical Co., Ltd. and Daiichi‐Sankyo Co., Ltd., scholarship endowments from Chugai Pharmaceutical Co., Ltd. and Taiho Pharmaceutical Co., Ltd., and is a member of the editorial board of . S.M. receives lecture fees, honoraria, or other fees from AstraZeneca K.K., Bristol‐Myers Squibb K.K., Chugai Pharmaceutical Co., Ltd., Eli Lilly and Company, MSD K.K., Pfizer Japan Inc., and Taiho Pharmaceutical Co., Ltd. M.T. (Toi) receives lecture fees, honoraria, or other fees from AstraZeneca K.K., Daiichi‐Sankyo Co., Ltd., and Eli Lilly and Company, research funds from AFI Corporation, Astellas Pharma Inc., AstraZeneca K.K., GL Sciences Inc., Kyoto Breast Cancer Research Network, Kyowa‐Kirin Co., Ltd., Shimadzu Corporation, Taiho Pharmaceutical Co., Ltd., and Yakult Honsha Co., Ltd., scholarship endowments from Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., and Nippon Kayaku Co., Ltd., and is a member of the editorial board of . S.O. receives lecture fees, honoraria, or other fees from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Eli Lilly and Company, and Pfizer Japan Inc., research funds from Eisai Co., Ltd., and is a member of the editorial board of . The other authors have no conflict of interest to disclose. Cancer Science Cancer Science Cancer Science Cancer Science Cancer Science
Funding Information:
This study was supported by the Japan Breast Cancer Research Group. Research funding was provided to the Japan Breast Cancer Research Group by Chugai Pharmaceutical Corporation under a research agreement. We would like to thank patients, their families, researchers from 93 institutions, and Clinical Research Coordinators for participating in the PRECIOUS trial. Patient registration, randomization, and data management were performed by Chikako Hibi and Shina Kurai of the JBCRG Data Center. The data were analyzed by Masao Shionoya of Mebics. Medical writing and editorial assistance were provided by Mark Snape, Yoshiko Okamoto, and Yasutomo Yutoku of inScience Communications, Springer Healthcare. Finally, I would like to express my gratitude to all the Japan Breast Cancer Research Group staff, including Michiro Soma, Nobuko Aoki, Kiyomi Nishizawa, and Mieko Abe, for their great contribution to the completion of this study.
Publisher Copyright:
© 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
PY - 2022
Y1 - 2022
N2 - No standard options existed for human epidermal growth factor receptor 2 (HER2)-positive advanced breast cancer that progresses after second-line trastuzumab emtansine therapy before 2020. The purpose of this study was to examine the efficacy of pertuzumab retreatment after disease progression following pertuzumab-containing therapy for HER2-positive locally advanced or metastatic breast cancer for the first time. This randomized, open-label, multicenter phase III trial was undertaken in 93 sites in Japan. Eligible patients with HER2-positive breast cancer who had received pertuzumab, trastuzumab, and chemotherapy as first- and/or second-line therapy were randomly assigned (1:1) to: (i) pertuzumab, trastuzumab, and physician's choice chemotherapy (PTC), or (ii) trastuzumab and physician's choice chemotherapy (TC). The primary end-point was investigator-assessed progression-free survival (PFS). Between August 1, 2015 and December 31, 2018, 219 patients were randomized to PTC (n = 110) or TC (n = 109). Median follow-up was 14.2 months (interquartile range, 9.0–22.2), and median PFS was 5.3 months (95% confidence interval [CI], 4.0–6.6) with PTC and 4.2 months (95% CI, 3.2–4.8) with TC (stratified hazard ratio 0.76 [95% CI upper limit 0.967]; p = 0.022). Progression-free survival was improved by adding pertuzumab in all prespecified subgroups. The PTC arm showed a trend towards better overall survival and duration of response, but similar objective response and health-related quality of life. The incidence of treatment-related adverse events was similar between groups except for diarrhea. Pertuzumab retreatment contributes to disease control for HER2-positive locally advanced or metastatic breast cancer previously treated with pertuzumab-containing regimens.
AB - No standard options existed for human epidermal growth factor receptor 2 (HER2)-positive advanced breast cancer that progresses after second-line trastuzumab emtansine therapy before 2020. The purpose of this study was to examine the efficacy of pertuzumab retreatment after disease progression following pertuzumab-containing therapy for HER2-positive locally advanced or metastatic breast cancer for the first time. This randomized, open-label, multicenter phase III trial was undertaken in 93 sites in Japan. Eligible patients with HER2-positive breast cancer who had received pertuzumab, trastuzumab, and chemotherapy as first- and/or second-line therapy were randomly assigned (1:1) to: (i) pertuzumab, trastuzumab, and physician's choice chemotherapy (PTC), or (ii) trastuzumab and physician's choice chemotherapy (TC). The primary end-point was investigator-assessed progression-free survival (PFS). Between August 1, 2015 and December 31, 2018, 219 patients were randomized to PTC (n = 110) or TC (n = 109). Median follow-up was 14.2 months (interquartile range, 9.0–22.2), and median PFS was 5.3 months (95% confidence interval [CI], 4.0–6.6) with PTC and 4.2 months (95% CI, 3.2–4.8) with TC (stratified hazard ratio 0.76 [95% CI upper limit 0.967]; p = 0.022). Progression-free survival was improved by adding pertuzumab in all prespecified subgroups. The PTC arm showed a trend towards better overall survival and duration of response, but similar objective response and health-related quality of life. The incidence of treatment-related adverse events was similar between groups except for diarrhea. Pertuzumab retreatment contributes to disease control for HER2-positive locally advanced or metastatic breast cancer previously treated with pertuzumab-containing regimens.
KW - advanced breast cancer
KW - heavily pretreated
KW - HER2-positive
KW - pertuzumab
KW - trastuzumab
UR - http://www.scopus.com/inward/record.url?scp=85134514604&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85134514604&partnerID=8YFLogxK
U2 - 10.1111/cas.15474
DO - 10.1111/cas.15474
M3 - Article
C2 - 35754298
AN - SCOPUS:85134514604
SN - 1347-9032
JO - Cancer Science
JF - Cancer Science
ER -