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- Title
Multicenter phase II study of trastuzumab with S-1 plus oxaliplatin for chemotherapy-naïve, HER2-positive advanced gastric cancer.
- Authors
Takahari, Daisuke; Chin, Keisho; Ishizuka, Naoki; Takashima, Atsuo; Minashi, Keiko; Kadowaki, Shigenori; Nishina, Tomohiro; Nakajima, Takako Eguchi; Amagai, Kenji; Machida, Nozomu; Goto, Masahiro; Taku, Keisei; Wakatsuki, Takeru; Shoji, Hirokazu; Hironaka, Shuichi; Boku, Narikazu; Yamaguchi, Kensei
- Abstract
Background: Trastuzumab with cisplatin and fluoropyrimidines improves overall survival (OS) in patients with HER2-positive advanced gastric cancer (AGC). S-1 plus oxaliplatin (SOX) is one of the standard regimens for HER2-negative AGC in Japan. However, few studies have evaluated trastuzumab combined with SOX in patients with HER2-positive AGC. Methods: This was a multicenter, phase II study conducted at 10 institutions in Japan. Patients with HER2-positive AGC received S-1 twice a day on days 1–14 and oxaliplatin and trastuzumab on day 1 of a 21-day cycle. The primary endpoint was the confirmed overall response rate (ORR), and the secondary endpoints were OS, progression-free survival (PFS), and safety. The sample size was 75 to have 90% power with an alpha error of 0.1 (one-sided), expecting an ORR of 65% and threshold of 50%. Results: From June 2015 to January 2018, 75 patients were enrolled. The ORR was 70.7% [95% confidence interval (CI) 59.0–80.6]. The median OS and PFS were estimated as 18.1 months (95% CI 15.6–26.5) and 8.8 months (95% CI 7.4–12.2), respectively. The major grade 3 or 4 adverse events were sensory neuropathy (16.0%) and neutropenia (10.7%). Conclusions: Trastuzumab with SOX had promising activity with well-tolerated toxicities for patients with HER2-positive AGC. Clinical trial registration: UMIN000017602.
- Subjects
JAPAN; STOMACH cancer; OXALIPLATIN; CLINICAL trial registries; TRASTUZUMAB; PROGRESSION-free survival
- Publication
Gastric Cancer, 2019, Vol 22, Issue 6, p1238
- ISSN
1436-3291
- Publication type
Article
- DOI
10.1007/s10120-019-00973-5