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Trastuzumab Deruxtecan in Anti-Human Epidermal Growth Factor Receptor 2 Treatment-Naive Patients With Human Epidermal Growth Factor Receptor 2-Low Gastric or Gastroesophageal Junction Adenocarcinoma: Exploratory Cohort Results in a Phase II Trial

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dc.contributor.authorYamaguchi, Kensei-
dc.contributor.authorBang, Yung-Jue-
dc.contributor.authorIwasa, Satoru-
dc.contributor.authorSugimoto, Naotoshi-
dc.contributor.authorRyu, Min-Hee-
dc.contributor.authorSakai, Daisuke-
dc.contributor.authorChung, Hyun Cheol-
dc.contributor.authorKawakami, Hisato-
dc.contributor.authorYabusaki, Hiroshi-
dc.contributor.authorLee, Jeeyun-
dc.contributor.authorShimoyama, Tatsu-
dc.contributor.authorLee, Keun-Wook-
dc.contributor.authorSaito, Kaku-
dc.contributor.authorKawaguchi, Yoshinori-
dc.contributor.authorKamio, Takahiro-
dc.contributor.authorKojima, Akihito-
dc.contributor.authorSugihara, Masahiro-
dc.contributor.authorShitara, Kohei-
dc.date.accessioned2023-03-16T02:11:44Z-
dc.date.available2023-03-16T02:11:44Z-
dc.date.created2023-03-07-
dc.date.created2023-03-07-
dc.date.created2023-03-07-
dc.date.created2023-03-07-
dc.date.created2023-03-07-
dc.date.created2023-03-07-
dc.date.created2023-03-07-
dc.date.created2023-03-07-
dc.date.issued2023-02-
dc.identifier.citationJournal of Clinical Oncology, Vol.41 No.4, pp.816-825-
dc.identifier.issn0732-183X-
dc.identifier.urihttps://hdl.handle.net/10371/189392-
dc.description.abstractPURPOSE: To investigate efficacy and safety of trastuzumab deruxtecan (T-DXd) in human epidermal growth factor receptor 2 (HER2)-low gastric or gastroesophageal junction (GEJ) adenocarcinoma. METHODS: Patients with locally advanced or metastatic HER2-low (cohort 1, immunohistochemistry 2+/in situ hybridization-negative; cohort 2, immunohistochemistry 1+) gastric/GEJ adenocarcinoma treated with at least two prior regimens, including fluoropyrimidine and platinum, but anti-HER2 therapy naive, received T-DXd 6.4 mg/kg intravenously once every 3 weeks. The primary end point was confirmed objective response rate by independent central review. RESULTS: Among 21 patients enrolled in cohort 1 and 24 enrolled in cohort 2, 19 and 21 patients, respectively, had central HER2 confirmation, received T-DXd, and had measurable tumors at baseline. The confirmed objective response rate was 26.3% (95% CI, 9.1 to 51.2) from five partial responses in cohort 1 and 9.5% (95% CI, 1.2 to 30.4) from two partial responses in cohort 2. Thirteen patients (68.4%) in cohort 1 and 12 (60.0%) in cohort 2 experienced reduced tumor size. The median overall survival was 7.8 months (95% CI, 4.7 to nonevaluable) in cohort 1 and 8.5 months (95% CI, 4.3 to 10.9) in cohort 2; the median progression-free survival was 4.4 months (95% CI, 2.7 to 7.1) and 2.8 months (95% CI, 1.5 to 4.3), respectively. The most common grade ≥ 3 treatment-emergent adverse events in cohorts 1 and 2 were anemia (30.0% and 29.2%), decreased neutrophil count (25.0% and 29.2%), and decreased appetite (20.0% and 20.8%). Drug-related interstitial lung disease/pneumonitis occurred in one patient in each cohort (grade 1 or 2). No drug-related deaths occurred. CONCLUSION: This study provides preliminary evidence that T-DXd has clinical activity in patients with heavily pretreated HER2-low gastric/GEJ adenocarcinoma.-
dc.language영어-
dc.publisherAmerican Society of Clinical Oncology-
dc.titleTrastuzumab Deruxtecan in Anti-Human Epidermal Growth Factor Receptor 2 Treatment-Naive Patients With Human Epidermal Growth Factor Receptor 2-Low Gastric or Gastroesophageal Junction Adenocarcinoma: Exploratory Cohort Results in a Phase II Trial-
dc.typeArticle-
dc.identifier.doi10.1200/JCO.22.00575-
dc.citation.journaltitleJournal of Clinical Oncology-
dc.identifier.wosid000940780800014-
dc.identifier.scopusid2-s2.0-85147088162-
dc.citation.endpage825-
dc.citation.number4-
dc.citation.startpage816-
dc.citation.volume41-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorBang, Yung-Jue-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusDRUG CONJUGATE-
dc.subject.keywordPlusDS-8201A-
dc.subject.keywordPlusHER2-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusTUMORS-
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  • Department of Medicine
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