PMID- 24801910 OWN - NLM STAT- MEDLINE DCOM- 20150113 LR - 20211021 IS - 1423-0380 (Electronic) IS - 1010-4283 (Linking) VI - 35 IP - 8 DP - 2014 Aug TI - The role of anti-VEGF agents in the treatment of advanced gastric cancer: a meta-analysis of randomized controlled trials. PG - 7675-83 LID - 10.1007/s13277-014-2037-3 [doi] AB - Inhibition of vascular epithelial growth factor (VEGF) signaling pathways has proven to be an effective strategy for the treatment of several common solid tumors, but its role in the management of advanced gastric cancer (AGC) is yet to be defined. We performed a meta-analysis of randomized controlled trials (RCTs) to assess the efficacy and safety of anti-VEGF agents in the treatment of AGC. Several databases were searched, including PubMed, Embase, and Cochrane databases. The endpoints were overall survival (OS), progression-free survival (PFS), overall response rate (ORR), and grade 3 or 4 adverse events (AEs). The pooled hazard ratio (HR) or relative risk (RR) and 95 % confidence intervals (CI) were calculated employing fixed- or random-effects models depending on the heterogeneity of the included trials. Seven RCTs which involved 2,340 patients were ultimately identified. The pooled analysis demonstrated that anti-VEGF therapy significantly improved OS (HR 0.74, 95 % CI 0.61-0.91, p = 0.003), PFS (HR 0.59, 95 % CI 0.44-0.78, p < 0.001), and ORR (RR 1.43, 95 % CI 1.14-1.79, p = 0.002) when compared to non-anti-VEGF therapy. Sensitivity analysis further confirmed this association. Additionally, more incidences of grade 3 or 4 thrombocytopenia, diarrhea, and hypertension were observed in anti-VEGF therapy. The anti-VEGF therapy offers a significant survival benefit in patients with AGC, especially for those previously treated patients, when compared to non-anti-VEGF therapy. With the present available data from randomized clinical trials, we could not clearly set the role of specific anti-VEGF agents in the treatment of AGC. Further studies are recommended to identify patients who could derive greater benefits from specific anti-VEGF agents. FAU - Qi, Wei-Xiang AU - Qi WX AD - Department of Oncology, Shanghai Jiao Tong University affiliated Sixth People's Hospital, No. 600, Yishan Road, Shanghai, 200233, China, qiweixiang1113@163.com. FAU - Shen, Zan AU - Shen Z FAU - Tang, Li-Na AU - Tang LN FAU - Yao, Yang AU - Yao Y LA - eng PT - Journal Article PT - Meta-Analysis DEP - 20140507 PL - Netherlands TA - Tumour Biol JT - Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine JID - 8409922 RN - 0 (Vascular Endothelial Growth Factor A) SB - IM MH - Disease-Free Survival MH - Humans MH - Publication Bias MH - Randomized Controlled Trials as Topic MH - Stomach Neoplasms/*drug therapy/mortality MH - Vascular Endothelial Growth Factor A/*antagonists & inhibitors EDAT- 2014/05/08 06:00 MHDA- 2015/01/15 06:00 CRDT- 2014/05/08 06:00 PHST- 2014/03/11 00:00 [received] PHST- 2014/04/28 00:00 [accepted] PHST- 2014/05/08 06:00 [entrez] PHST- 2014/05/08 06:00 [pubmed] PHST- 2015/01/15 06:00 [medline] AID - 10.1007/s13277-014-2037-3 [doi] PST - ppublish SO - Tumour Biol. 2014 Aug;35(8):7675-83. doi: 10.1007/s13277-014-2037-3. Epub 2014 May 7.