Please use this identifier to cite or link to this item: 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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