PD-L1 and gastric cancer prognosis: A systematic review and meta-analysis.
PD-L1 and gastric cancer prognosis: A systematic review and meta-analysis.
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DOI:
10.1371/journal.pone.0182692
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发表时间:
2017
期刊:
影响因子:
3.7
通讯作者:
Wang X
中科院分区:
文献类型:
--
作者:
Gu L;Chen M;Guo D;Zhu H;Zhang W;Pan J;Zhong X;Li X;Qian H;Wang X
The expression of Programmed cell Death Ligand 1 (PD-L1) is observed in many malignant tumors and is associated with poor prognosis including Gastric Cancer (GC). The relationship between PD-L1 expression and prognosis, however, is controversial in GC. This paper purports to use a meta-analysis to investigate the relationship between PD-L1 expression and prognosis in GC. For this study, the following databases were searched for articles published from June 2003 until February 2017: PubMed, EBSCO, Web of Science and Cochrane Library. The baseline information extracted were: authors, year of publication, country where the study was performed, study design, sample size, follow-up time, baseline characteristics of the study population, pathologic data, overall survival (OS). A total of 15 eligible studies covering 3291 patients were selected for a meta-analysis based on specified inclusion and exclusion criteria. The analysis showed that the expression level of PD-L1 was associated with the overall survival in GC (Hazard Ratio, HR = 1.46, 95%CI = 1.08–1.98, P = 0.01, random-effect). In addition to the above, subgroup analysis showed that GC patients with deeper tumor infiltration, positive lymph-node metastasis, positive venous invasion, Epstein-Barr virus infection positive (EBV+), Microsatellite Instability (MSI) are more likely to expression PD-L1. The results of this meta-analysis suggest that GC patients, specifically EBV+ and MSI, may be prime candidates for PD-1 directed therapy. These findings support anti-PD-L1/PD-1 antibodies as a kind of immunotherapy which is promising for GC.
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影响因子:
--
作者:
Chang H;Jung WY;Kang Y;Lee H;Kim A;Kim HK;Shin BK;Kim BH
通讯作者:
Kim BH
影响因子:
15.8
作者:
Moher D;Liberati A;Tetzlaff J;Altman DG;PRISMA Group
通讯作者:
PRISMA Group
DOI:
10.2147/dddt.s75152
发表时间:
2015
期刊:
Drug design, development and therapy
影响因子:
--
作者:
Qing Y;Li Q;Ren T;Xia W;Peng Y;Liu GL;Luo H;Yang YX;Dai XY;Zhou SF;Wang D
通讯作者:
Wang D
影响因子:
--
作者:
Derks S;Liao X;Chiaravalli AM;Xu X;Camargo MC;Solcia E;Sessa F;Fleitas T;Freeman GJ;Rodig SJ;Rabkin CS;Bass AJ
通讯作者:
Bass AJ
影响因子:
3.8
作者:
Liu, Xin;Chen, Kunqi;Na, Zhenyu
通讯作者:
Na, Zhenyu