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Trastuzumab Deruxtecan after Endocrine Therapy in Metastatic Breast Cancer

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dc.contributor.authorBardia, Aditya-
dc.contributor.authorHu, X.-
dc.contributor.authorDent, Rebecca-
dc.contributor.authorYonemori, Kan-
dc.contributor.authorBarrios, Carlos H.-
dc.contributor.authorO'Shaughnessy, Joyce A.-
dc.contributor.authorWildiers, Hans-
dc.contributor.authorPierga, Jean-Yves-
dc.contributor.authorZhang, Qingyuan-
dc.contributor.authorSaura, Cristina-
dc.contributor.authorBiganzoli, Laura-
dc.contributor.authorSohn, Joohyuk-
dc.contributor.authorIm, Seock-Ah-
dc.contributor.authorLevy, Christelle-
dc.contributor.authorJacot, William-
dc.contributor.authorBegbie, Natasha-
dc.contributor.authorKe, Jun-
dc.contributor.authorPatel, Gargi-
dc.contributor.authorCurigliano, Giuseppe-
dc.date.accessioned2025-02-03T09:27:41Z-
dc.date.available2025-02-03T09:27:41Z-
dc.date.created2025-03-20-
dc.date.issued2024-12-
dc.identifier.issn0028-4793-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/202488-
dc.description.abstractBackground Outcomes in patients with hormone receptor-positive metastatic breast cancer worsen after one or more lines of endocrine-based therapy. Trastuzumab deruxtecan has shown efficacy in patients with metastatic breast cancer with low expression of human epidermal growth factor receptor 2 (HER2) after previous chemotherapy. Methods We conducted a phase 3, multicenter, open-label trial involving patients with hormone receptor-positive metastatic breast cancer with low HER2 expression (a score of 1+ or 2+ on immunohistochemical [IHC] analysis and negative results on in situ hybridization) or ultralow HER2 expression (IHC 0 with membrane staining) who had received one or more lines of endocrine-based therapy and no previous chemotherapy for metastatic breast cancer. Patients were randomly assigned in a 1:1 ratio to receive trastuzumab deruxtecan or the physician&apos;s choice of chemotherapy. The primary end point was progression-free survival (according to blinded independent central review) among the patients with HER2-low disease. Secondary end points included progression-free survival among all the patients who had undergone randomization, overall survival, and safety. Results Of the 866 patients who underwent randomization, 713 had HER2-low disease, and 153 had HER2-ultralow disease. Among the patients with HER2-low disease, the median progression-free survival was 13.2 months (95% confidence interval [CI], 11.4 to 15.2) in the trastuzumab deruxtecan group and 8.1 months (95% CI, 7.0 to 9.0) in the chemotherapy group (hazard ratio for disease progression or death, 0.62; 95% CI, 0.52 to 0.75; P<0.001); the results were consistent in the exploratory HER2-ultralow population. Data for overall survival were immature. Adverse events of grade 3 or higher occurred in 52.8% of the patients in the trastuzumab deruxtecan group and in 44.4% of those in the chemotherapy group. Adjudicated interstitial lung disease or pneumonitis occurred in 49 patients (11.3%; three events were grade 5 in severity) and in 1 patient (0.2%; grade 2), respectively. Conclusions Among patients with hormone receptor-positive, HER2-low or HER2-ultralow metastatic breast cancer who had received one or more lines of endocrine-based therapy, treatment with trastuzumab deruxtecan resulted in longer progression-free survival than chemotherapy. No new safety signals were identified.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherMassachusetts Medical Society-
dc.relation.isPartOfNEW ENGLAND JOURNAL OF MEDICINE-
dc.relation.isPartOfNEW ENGLAND JOURNAL OF MEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleTrastuzumab Deruxtecan after Endocrine Therapy in Metastatic Breast Cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorBardia, Aditya-
dc.contributor.googleauthorHu, X.-
dc.contributor.googleauthorDent, Rebecca-
dc.contributor.googleauthorYonemori, Kan-
dc.contributor.googleauthorBarrios, Carlos H.-
dc.contributor.googleauthorO&apos;Shaughnessy, Joyce A.-
dc.contributor.googleauthorWildiers, Hans-
dc.contributor.googleauthorPierga, Jean-Yves-
dc.contributor.googleauthorZhang, Qingyuan-
dc.contributor.googleauthorSaura, Cristina-
dc.contributor.googleauthorBiganzoli, Laura-
dc.contributor.googleauthorSohn, Joohyuk-
dc.contributor.googleauthorIm, Seock-Ah-
dc.contributor.googleauthorLevy, Christelle-
dc.contributor.googleauthorJacot, William-
dc.contributor.googleauthorBegbie, Natasha-
dc.contributor.googleauthorKe, Jun-
dc.contributor.googleauthorPatel, Gargi-
dc.contributor.googleauthorCurigliano, Giuseppe-
dc.identifier.doi10.1056/NEJMoa2407086-
dc.relation.journalcodeJ02371-
dc.identifier.eissn1533-4406-
dc.identifier.pmid39282896-
dc.subject.keywordBreast Cancer-
dc.subject.keywordHematology/Oncology-
dc.subject.keywordTreatments in Oncology-
dc.contributor.alternativeNameSohn, Joo Hyuk-
dc.contributor.affiliatedAuthorSohn, Joohyuk-
dc.identifier.scopusid2-s2.0-85211967365-
dc.identifier.wosid001412990600005-
dc.citation.volume391-
dc.citation.number22-
dc.citation.startPage2110-
dc.citation.endPage2122-
dc.identifier.bibliographicCitationNEW ENGLAND JOURNAL OF MEDICINE, Vol.391(22) : 2110-2122, 2024-12-
dc.identifier.rimsid85462-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorBreast Cancer-
dc.subject.keywordAuthorHematology/Oncology-
dc.subject.keywordAuthorTreatments in Oncology-
dc.subject.keywordPlusGUIDELINE-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusDS-8201A-
dc.subject.keywordPlusHER2-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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