Trastuzumab deruxtecan in previously treated HER2-low advanced breast cancer Journal Article


Authors: Modi, S.; Jacot, W.; Yamashita, T.; Sohn, J.; Vidal, M.; Tokunaga, E.; Tsurutani, J.; Ueno, N. T.; Prat, A.; Chae, Y. S.; Lee, K. S.; Niikura, N.; Park, Y. H.; Xu, B.; Wang, X.; Gil-Gil, M.; Li, W.; Pierga, J. Y.; Im, S. A.; Moore, H. C. F.; Rugo, H. S.; Yerushalmi, R.; Zagouri, F.; Gombos, A.; Kim, S. B.; Liu, Q.; Luo, T.; Saura, C.; Schmid, P.; Sun, T.; Gambhire, D.; Yung, L.; Wang, Y.; Singh, J.; Vitazka, P.; Meinhardt, G.; Harbeck, N.; Cameron, D. A.; for the DESTINY-Breast04 Trial Investigators
Article Title: Trastuzumab deruxtecan in previously treated HER2-low advanced breast cancer
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. © 2022 Massachusetts Medical Society.
Keywords: controlled study; antineoplastic agent; randomized controlled trial; antineoplastic combined chemotherapy protocols; epidermal growth factor receptor 2; camptothecin; pathology; breast neoplasms; monoclonal antibody; disease progression; breast tumor; receptor, erbb-2; trastuzumab; disease exacerbation; antibody conjugate; immunoconjugates; antibodies, monoclonal, humanized; humans; human; female; trastuzumab deruxtecan
Journal Title: New England Journal of Medicine
Volume: 387
Issue: 1
ISSN: 0028-4793
Publisher: Massachusetts Medical Society  
Date Published: 2022-07-07
Start Page: 9
End Page: 20
Language: English
DOI: 10.1056/NEJMoa2203690
PUBMED: 35665782
PROVIDER: scopus
PMCID: PMC10561652
DOI/URL:
Notes: Article -- Export Date: 1 August 2022 -- Source: Scopus
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  1. Shanu Modi
    267 Modi