Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/197309
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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.identifier.issn0028-4793-
dc.identifier.urihttps://hdl.handle.net/2445/197309-
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.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.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-
dc.date.updated2023-04-26T12:47:48Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.idimarina9315826-
dc.identifier.pmid35665782-
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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