A phase 2 trial of intravenous and intraperitoneal paclitaxel combined with S-1 for treatment of gastric cancer with macroscopic peritoneal metastasis
Version of Record online: 24 JUN 2013
© 2013 American Cancer Society
Volume 119, Issue 18, pages 3354–3358, 15 September 2013
How to Cite
Yamaguchi, H., Kitayama, J., Ishigami, H., Emoto, S., Yamashita, H. and Watanabe, T. (2013), A phase 2 trial of intravenous and intraperitoneal paclitaxel combined with S-1 for treatment of gastric cancer with macroscopic peritoneal metastasis. Cancer, 119: 3354–3358. doi: 10.1002/cncr.28204
- Issue online: 4 SEP 2013
- Version of Record online: 24 JUN 2013
- Manuscript Accepted: 13 MAY 2013
- Manuscript Revised: 3 MAY 2013
- Manuscript Received: 19 JAN 2013
- phase 2 study;
- gastric cancer;
- peritoneal metastasis;
- intraperitoneal chemotherapy
The prognosis of patients with gastric cancer with peritoneal metastasis is extremely poor. This phase 2 study evaluated the benefits and tolerability of weekly intravenous and intraperitoneal paclitaxel (PTX) treatment combined with oral S-1 in patients with gastric cancer who had macroscopic peritoneal metastasis.
Patients with gastric cancer who had primary tumors with macroscopic peritoneal metastasis were enrolled. PTX was administered intravenously at 50 mg/m2 and intraperitoneally at 20 mg/m2 on days 1 and 8, respectively. S-1 was administered at 80 mg/m2 per day for 14 consecutive days, followed by 7 days of rest. The primary endpoint was the 1-year overall survival (OS) rate. The secondary endpoints were the response rate, efficacy against malignant ascites, and safety.
Thirty-five patients were enrolled. The median number of treatment courses was 11 (range, 2-35). The 1-year OS rate was 77.1% (95% confidence interval, 60.5-88.1). The overall response rate was 71% in 7 patients with target lesions. Malignant ascites disappeared or decreased in 15 of 22 (68%) patients. The frequent grade 3/4 toxic effects were neutropenia (34%), leukopenia (23%), and anemia (9%).
Combination chemotherapy consisting of intravenous and intraperitoneal PTX with S-1 is well-tolerated and effective in patients with gastric cancer who have macroscopic peritoneal metastasis. Cancer 2013;119:3354–8. © 2013 American Cancer Society.