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Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer

Authors
 Modi, Shanu  ;  Jacot, William  ;  Yamashita, Toshinari  ;  Sohn, Joo Hyuk  ;  Vidal, Maria  ;  Tokunaga, Eriko  ;  Tsurutani, Junji  ;  Ueno, Naoto T.  ;  Prat, 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  ;  Kim, 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  ;  Cameron, David A. 
Citation
 New England Journal of Medicine, Vol.387(1) : 9-20, 2022-07 
Journal Title
NEW ENGLAND JOURNAL OF MEDICINE
ISSN
 0028-4793 
Issue Date
2022-07
Abstract
BACKGROUND 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. METHODS 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. RESULTS 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. CONCLUSIONS 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, .)
DOI
10.1056/NEJMoa2203690
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Sohn, Joo Hyuk(손주혁) ORCID logo https://orcid.org/0000-0002-2303-2764
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/191707
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