Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer

dc.contributor.authorModi, Shaun
dc.contributor.authorJacot, William
dc.contributor.authorYamashita, Toshinari
dc.contributor.authorSohn, Joohyuk
dc.contributor.authorVidal, Maria
dc.contributor.authorTokunaga, Eriko
dc.contributor.authorTsurutani, Junji
dc.contributor.authorUeno,Naoto T.
dc.contributor.authorPrat Aparicio, Aleix
dc.contributor.authorChae, Yee Soo
dc.contributor.authorLee, Keun Seok
dc.contributor.authorNiikura, Naoki
dc.contributor.authorPark, Yeon Hee
dc.contributor.authorXu, Binghe
dc.contributor.authorWang, Xiaojia
dc.contributor.authorGil Gil, Miguel
dc.contributor.authorLi, Wei
dc.contributor.authorPierga, Jean Yves
dc.contributor.authorIm, Seock-Ah
dc.contributor.authorMoore, Halle C.F.
dc.contributor.authorRugo, Hope S.
dc.contributor.authorYerushalmi, Rinat
dc.contributor.authorZagouri, Flora
dc.contributor.authorGombos, Andrea
dc.contributor.authorKi, Sung Bae
dc.contributor.authorLiu, Qiang
dc.contributor.authorLuo, Ting
dc.contributor.authorSaura, Cristina
dc.contributor.authorSchmid, Peter
dc.contributor.authorSun,Tao
dc.contributor.authorGambhire, Dhiraj
dc.contributor.authorYung, Lotus
dc.contributor.authorWang, Yibin
dc.contributor.authorSingh, Jasmeet
dc.contributor.authorVitazka, Patrik
dc.contributor.authorMeinhardt, Gerold
dc.contributor.authorHarbeck, Nadia
dc.contributor.authorCamero, David A.
dc.date.accessioned2023-04-26T14:11:53Z
dc.date.available2023-04-26T14:11:53Z
dc.date.issued2022-07-07
dc.date.updated2023-04-26T12:47:48Z
dc.description.abstractAmong 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.
dc.format.extent12 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idimarina9315826
dc.identifier.issn0028-4793
dc.identifier.pmid35665782
dc.identifier.urihttps://hdl.handle.net/2445/197309
dc.language.isoeng
dc.publisherNEJM Group
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1056/nejmoa2203690
dc.relation.ispartofNew England Journal Of Medicine, 2022, vol. 387, num. 1, p. 9-20
dc.relation.urihttps://doi.org/10.1056/nejmoa2203690
dc.rights(c) NEJM, 2022
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
dc.subject.classificationCàncer de mama
dc.subject.classificationAnticossos monoclonals
dc.subject.otherBreast cancer
dc.subject.otherMonoclonal antibodies
dc.titleTrastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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