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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 Trialopen access

Authors
Yamaguchi, K.[Yamaguchi, K.]Bang, Y.-J.[Bang, Y.-J.]Iwasa, S.[Iwasa, S.]Sugimoto, N.[Sugimoto, N.]Ryu, M.-H.[Ryu, M.-H.]Sakai, D.[Sakai, D.]Chung, H.C.[Chung, H.C.]Kawakami, H.[Kawakami, H.]Yabusaki, H.[Yabusaki, H.]Lee, J.[Lee, J.]Shimoyama, T.[Shimoyama, T.]Lee, K.-W.[Lee, K.-W.]Saito, K.[Saito, K.]Kawaguchi, Y.[Kawaguchi, Y.]Kamio, T.[Kamio, T.]Kojima, A.[Kojima, A.]Sugihara, M.[Sugihara, M.]Shitara, K.[Shitara, K.]
Issue Date
1-Feb-2023
Publisher
Lippincott Williams and Wilkins
Citation
Journal of Clinical Oncology, v.41, no.4, pp.816 - 825
Indexed
SCIE
SCOPUS
Journal Title
Journal of Clinical Oncology
Volume
41
Number
4
Start Page
816
End Page
825
URI
https://scholarx.skku.edu/handle/2021.sw.skku/103512
DOI
10.1200/JCO.22.00575
ISSN
0732-183X
Abstract
PURPOSETo investigate efficacy and safety of trastuzumab deruxtecan (T-DXd) in human epidermal growth factor receptor 2 (HER2)-low gastric or gastroesophageal junction (GEJ) adenocarcinoma.METHODSPatients 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.RESULTSAmong 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.CONCLUSIONThis study provides preliminary evidence that T-DXd has clinical activity in patients with heavily pretreated HER2-low gastric/GEJ adenocarcinoma. © American Society of Clinical Oncology.
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