Phase II study of S-1 plus docetaxel as first-line treatment for older patients with advanced gastric cancer (OGSG 0902)

Author:

Kawase Tomono1,IMAMURA HIROSHI1ORCID,Kawabata Ryohei2,Matsuyama Jin3,Nishikawa Kazuhiro2,Yanagihara Kazuhiro4,Yamamoto Kazuyoshi5,Hoki Noriyuki6,Kawada Junji7,Kawakami Hisato8,Sakai Daisuke9,Kurokawa Yukinori10,Shimokawa Toshio11,Satoh Taroh10

Affiliation:

1. Toyonaka Municipal Hospital

2. Sakai City Medical Center: Sakai Shiritsu Sogo Iryo Center

3. Higashiosaka City Medical Center

4. Kansai Electric Power Hospital: Kansai Denryoku Byoin

5. Osaka University School of Medicine Graduate School of Medicine: Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu

6. Bellland General Hospital

7. Yao Municipal Hospital: Yao Shiritsu Byoin

8. Kindai University Faculty of Medicine Graduate School of Medical Sciences: Kinki Daigaku Igakubu Daigakuin Igaku Kenkyuka

9. Osaka International Cancer Institute: Osaka Kokusai Gan Center

10. Osaka University Faculty of Medicine Graduate School of Medicine: Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu

11. Wakayama Medical University: Wakayama Kenritsu Ika Daigaku

Abstract

Abstract Background Although there is insufficient evidence for the treatment of older patients with advanced gastric cancer, fluorouracil combined with platinum chemotherapy has been recognized as a standard first-line treatment for such populations in Japan despite the lack of efficacy and toxicity data. Methods Patients aged 75 years or older with advanced gastric cancer were enrolled. S-1 plus docetaxel (docetaxel: 40 mg/m2, day 1; S-1: 80 mg/m2, days 1–14; q21 days) was repeated every 3 weeks. The primary endpoint was overall response rate. Secondary endpoints were safety, progression-free survival, time to treatment failure, and overall survival. The sample size was calculated as 30 under the hypothesis of an expected response rate of 40% and a threshold response rate of 20%, at a power of 90% and a two-sided alpha value of 5%. Results From February 2010 to January 2015, 31 patients were enrolled and assessed for efficacy and toxicity. The response rate was 45.2% (95% CI: 27.3–64.0%; p = 0.001) and it exceeded the expected response rate set at 40%. Median progression-free survival was 5.8 months, the 1-year survival rate was 58.1%, and the median survival time was 16.1 months. The major grade 3/4 adverse events were neutropenia (58%), febrile neutropenia (13%), anemia (10%), anorexia (10%), and fatigue (6%). Conclusions These findings indicate that S-1 plus docetaxel as first-line treatment for older patients is feasible and that it has promising efficacy against advanced gastric cancer.

Publisher

Research Square Platform LLC

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