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http://hdl.handle.net/2445/197309
Title: | Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer |
Author: | Modi, Shaun Jacot, William Yamashita, Toshinari Sohn, Joohyuk Vidal, Maria Tokunaga, Eriko Tsurutani, Junji Ueno,Naoto T. Prat Aparicio, Aleix Chae, Yee Soo Lee, Keun Seok Niikura, Naoki Park, Yeon Hee Xu, Binghe Wang, Xiaojia Gil Gil, Miguel Li, Wei Pierga, Jean Yves Im, Seock-Ah Moore, Halle C.F. Rugo, Hope S. Yerushalmi, Rinat Zagouri, Flora Gombos, Andrea Ki, Sung Bae Liu, Qiang Luo, Ting Saura, Cristina Schmid, Peter Sun,Tao Gambhire, Dhiraj Yung, Lotus Wang, Yibin Singh, Jasmeet Vitazka, Patrik Meinhardt, Gerold Harbeck, Nadia Camero, David A. |
Keywords: | Càncer de mama Anticossos monoclonals Breast cancer Monoclonal antibodies |
Issue Date: | 7-Jul-2022 |
Publisher: | NEJM Group |
Abstract: | Among breast cancers without human epidermal growth factor receptor 2 (HER2) amplification, overexpression, or both, a large proportion express low levels of HER2 that may be targetable. Currently available HER2-directed therapies have been ineffective in patients with these "HER2-low" cancers.We conducted a phase 3 trial involving patients with HER2-low metastatic breast cancer who had received one or two previous lines of chemotherapy. (Low expression of HER2 was defined as a score of 1+ on immunohistochemical [IHC] analysis or as an IHC score of 2+ and negative results on in situ hybridization.) Patients were randomly assigned in a 2:1 ratio to receive trastuzumab deruxtecan or the physician's choice of chemotherapy. The primary end point was progression-free survival in the hormone receptor-positive cohort. The key secondary end points were progression-free survival among all patients and overall survival in the hormone receptor-positive cohort and among all patients.Of 557 patients who underwent randomization, 494 (88.7%) had hormone receptor-positive disease and 63 (11.3%) had hormone receptor-negative disease. In the hormone receptor-positive cohort, the median progression-free survival was 10.1 months in the trastuzumab deruxtecan group and 5.4 months in the physician's choice group (hazard ratio for disease progression or death, 0.51; P<0.001), and overall survival was 23.9 months and 17.5 months, respectively (hazard ratio for death, 0.64; P?=?0.003). Among all patients, the median progression-free survival was 9.9 months in the trastuzumab deruxtecan group and 5.1 months in the physician's choice group (hazard ratio for disease progression or death, 0.50; P<0.001), and overall survival was 23.4 months and 16.8 months, respectively (hazard ratio for death, 0.64; P?=?0.001). Adverse events of grade 3 or higher occurred in 52.6% of the patients who received trastuzumab deruxtecan and 67.4% of those who received the physician's choice of chemotherapy. Adjudicated, drug-related interstitial lung disease or pneumonitis occurred in 12.1% of the patients who received trastuzumab deruxtecan; 0.8% had grade 5 events.In this trial involving patients with HER2-low metastatic breast cancer, trastuzumab deruxtecan resulted in significantly longer progression-free and overall survival than the physician's choice of chemotherapy. (Funded by Daiichi Sankyo and AstraZeneca; DESTINY-Breast04 ClinicalTrials.gov number, NCT03734029.).Copyright © 2022 Massachusetts Medical Society. |
Note: | Reproducció del document publicat a: https://doi.org/10.1056/nejmoa2203690 |
It is part of: | New England Journal Of Medicine, 2022, vol. 387, num. 1, p. 9-20 |
URI: | http://hdl.handle.net/2445/197309 |
Related resource: | https://doi.org/10.1056/nejmoa2203690 |
ISSN: | 0028-4793 |
Appears in Collections: | Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer) Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) |
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