Published online Apr 14, 2015. doi: 10.3748/wjg.v21.i14.4358
Peer-review started: July 16, 2014
First decision: August 15, 2014
Revised: September 12, 2014
Accepted: October 21, 2014
Article in press: October 21, 2014
Published online: April 14, 2015
Processing time: 273 Days and 11.4 Hours
AIM: To rationally evaluate the effect of S-1 vs capecitabine for the treatment of gastric cancer.
METHODS: MEDLINE, EMBASE, Cochrane Controlled Trials Register, Google Scholar, and China Journal Full Text Database were accessed to collect clinical randomized controlled trials regarding the effect of S-1 vs capecitabine for the treatment of gastric cancer patients. Statistical analysis was performed by meta-analysis. Four randomized controlled trials met the inclusion criteria.
RESULTS: Compared with capecitabine regimens, the 1-year survival rate in gastric cancer patients was 0.80 (95%CI: 0.52-1.21, P = 0.29). The overall response rate of S-1 vs capecitabine was 0.94 (95%CI: 0.59-1.51, P = 0.93). Compared with capecitabine regimens, the most frequent hematologic toxicities were neutropenia (OR = 0.99, 95%CI: 0.65-1.49, P = 0.94) and thrombocytopenia (OR = 0.72, 95%CI: 0.31-1.67, P = 0.44). The most frequent non-hematologic toxicities included nausea (OR = 0.85, 95%CI: 0.56-1.28, P = 0.43) and hand-foot syndrome (OR = 0.16, 95%CI: 0.10-0.27, P < 0.00001).
CONCLUSION: The existing studies suggest that S-1 is not more effective than capecitabine in the treatment of gastric cancer patients, but does exhibit less toxicity with regard to hand-foot syndrome.
Core tip: Systemic chemotherapy has proven to be an important treatment for advanced gastric cancer patients. A combination regimen containing 5-fluorouracil is most commonly used worldwide. S-1 and capecitabine are both oral fluoropyrimidine carbamates, and have proven to be effective for the treatment of gastric cancer patients. This is the first meta-analysis to systematically compare the effects between S-1 and capecitabine against gastric cancer in order to better understand the efficacy, safety, and feasibility of these anticancer drugs. The results may contribute to better treatment and quality of life for patients with advanced gastric cancer.