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Trastuzumab deruxtecan versus trastuzumab emtansine in Asian patients with HER2-positive metastatic breast cancer

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dc.contributor.authorIwata, Hiroji-
dc.contributor.authorXu, Binghe-
dc.contributor.authorKim, Sung-Bae-
dc.contributor.authorChung, Wei-Pang-
dc.contributor.authorPark, Yeon Hee-
dc.contributor.authorKim, Min Hwan-
dc.contributor.authorTseng, Ling-Ming-
dc.contributor.authorChung, Chi-Feng-
dc.contributor.authorHuang, Chiun-Sheng-
dc.contributor.authorKim, Jee Hyun-
dc.contributor.authorChiu, Joanne Wing Yan-
dc.contributor.authorYamashita, Toshinari-
dc.contributor.authorLi, Wei-
dc.contributor.authorEgorov, Anton-
dc.contributor.authorNishijima, Soichiro-
dc.contributor.authorNakatani, Shunsuke-
dc.contributor.authorNishiyama, Yuji-
dc.contributor.authorSugihara, Masahiro-
dc.contributor.authorCortes, Javier-
dc.contributor.authorIm, Seock-Ah-
dc.date.accessioned2025-07-09T08:31:34Z-
dc.date.available2025-07-09T08:31:34Z-
dc.date.created2025-03-31-
dc.date.issued2024-09-
dc.identifier.issn1347-9032-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/206420-
dc.description.abstractThe global phase 3 DESTINY-Breast03 study (; NCT03529110) showed statistically significant and clinically meaningful improvements in progression-free survival (PFS) and overall survival (OS) with trastuzumab deruxtecan (T-DXd) over trastuzumab emtansine (T-DM1) in patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer (mBC) previously treated with trastuzumab and a taxane. Here, we report a subgroup analysis of Asian patients enrolled in DESTINY-Breast03. In total, 309 patients (149 in the T-DXd arm and 160 in the T-DM1 arm) from Asian countries and regions were randomized. At data cutoff (July 25, 2022), the median duration of follow-up in the Asian subpopulation was 29.0 months with T-DXd and 26.0 months with T-DM1. The PFS (determined by blinded independent central review) hazard ratio was 0.30 (95% confidence interval 0.22-0.41) favoring T-DXd over T-DM1 (median PFS 25.1 vs. 5.4 months). Median OS was not reached in the T-DXd arm and was 37.7 months in the T-DM1 arm. The median treatment duration was 15.4 months with T-DXd and 5.5 months with T-DM1. The incidence of grade >= 3 drug-related treatment-emergent adverse events was similar between both treatment arms (49.0% vs. 46.5%) and was consistent with the overall DESTINY-Breast03 population. Adjudicated drug-related interstitial lung disease or pneumonitis occurred in 12.9% of patients treated with T-DXd and 2.5% treated with T-DM1, with a higher incidence in Japanese patients; none of these were grade >= 4 events. These efficacy and safety data reinforce the favorable benefit-risk profile of T-DXd in HER2-positive mBC, including in the Asian subgroup. We report a subgroup analysis of Asian patients in DESTINY-Breast03. The efficacy and safety data reinforced the favorable benefit-risk profile of trastuzumab deruxtecan (T-DXd) in HER2-positive metastatic breast cancer within the Asian subgroup.image-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherWiley Publishing on behalf of the Japanese Cancer Association-
dc.relation.isPartOfCANCER SCIENCE-
dc.relation.isPartOfCANCER SCIENCE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleTrastuzumab deruxtecan versus trastuzumab emtansine in Asian patients with HER2-positive metastatic breast cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorIwata, Hiroji-
dc.contributor.googleauthorXu, Binghe-
dc.contributor.googleauthorKim, Sung-Bae-
dc.contributor.googleauthorChung, Wei-Pang-
dc.contributor.googleauthorPark, Yeon Hee-
dc.contributor.googleauthorKim, Min Hwan-
dc.contributor.googleauthorTseng, Ling-Ming-
dc.contributor.googleauthorChung, Chi-Feng-
dc.contributor.googleauthorHuang, Chiun-Sheng-
dc.contributor.googleauthorKim, Jee Hyun-
dc.contributor.googleauthorChiu, Joanne Wing Yan-
dc.contributor.googleauthorYamashita, Toshinari-
dc.contributor.googleauthorLi, Wei-
dc.contributor.googleauthorEgorov, Anton-
dc.contributor.googleauthorNishijima, Soichiro-
dc.contributor.googleauthorNakatani, Shunsuke-
dc.contributor.googleauthorNishiyama, Yuji-
dc.contributor.googleauthorSugihara, Masahiro-
dc.contributor.googleauthorCortes, Javier-
dc.contributor.googleauthorIm, Seock-Ah-
dc.identifier.doi10.1111/cas.16234-
dc.relation.journalcodeJ00454-
dc.identifier.eissn1349-7006-
dc.identifier.pmid38979893-
dc.subject.keywordbreast cancer-
dc.subject.keywordEast Asia-
dc.subject.keywordErbB-2 receptor-
dc.subject.keywordtrastuzumab deruxtecan-
dc.subject.keywordtrastuzumab emtansine-
dc.contributor.alternativeNameKim, Min Hwan-
dc.contributor.affiliatedAuthorKim, Min Hwan-
dc.identifier.scopusid2-s2.0-85197759851-
dc.identifier.wosid001268058500001-
dc.citation.volume115-
dc.citation.number9-
dc.citation.startPage3079-
dc.citation.endPage3088-
dc.identifier.bibliographicCitationCANCER SCIENCE, Vol.115(9) : 3079-3088, 2024-09-
dc.identifier.rimsid86190-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorbreast cancer-
dc.subject.keywordAuthorEast Asia-
dc.subject.keywordAuthorErbB-2 receptor-
dc.subject.keywordAuthortrastuzumab deruxtecan-
dc.subject.keywordAuthortrastuzumab emtansine-
dc.subject.keywordPlusOPEN-LABEL-
dc.subject.keywordPlusPERTUZUMAB-
dc.subject.keywordPlusDOCETAXEL-
dc.subject.keywordPlusDIAGNOSIS-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalResearchAreaOncology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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