The predictive value of tumor mutation burden on survival of gastric cancer patients treated with immune checkpoint inhibitors: A systematic review and meta-analysis

被引:10
作者
Ke, Liyuan [1 ]
Li, Su [1 ]
Huang, Danxue [1 ]
机构
[1] China Med Univ, Liaoning Canc Hosp & Inst, Dept Pharm, Canc Hosp, Shenyang, Peoples R China
关键词
Tumor mutation burden; Immune checkpoint inhibitors; Gastric cancer; Overall survival; Progression-free survival; Meta-analysis; PLUS CHEMOTHERAPY; IMMUNOTHERAPY; ASSOCIATION; NEOANTIGENS; SENSITIVITY; BIOMARKER; EFFICACY; BENEFIT; CHEMO;
D O I
10.1016/j.intimp.2023.110986
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Tumor mutation burden (TMB) is a complement to traditional biomarkers related to the efficacy of immune checkpoint inhibitors (ICIs). The relationship between TMB and the efficacy of ICIs in gastric cancer was controversial. The systematic review and meta-analysis were conducted to investigate the predictive value of TMB on survival of gastric cancer patients treated with ICIs.Methods: We searched the databases PubMed, Embase, and Web of Science for articles, then screened eligible articles according to inclusion criteria. The effective data were extracted to calculate the pooled effects of hazard ratio (HR) for overall survival (OS) and progression-free survival (PFS), then perform publication bias, sensitivity analysis, and subgroup analysis by STATA 16.0.Results: The high TMB patients showed significantly longer survival than the low TMB patients (OS: HR 0.65,95% CI 0.55, 0.77, p < 0.001; PFS: HR 0.51, 95% CI 0.33, 0.77, p = 0.001). In the Asian subgroup, patients with high TMB exhibited better prognosis compared to low TMB (OS: HR 0.56, 95% CI 0.43, 0.72, p < 0.001; PFS: HR 0.45, 95% CI 0.28, 0.72, p = 0.001). In the non-Asian subgroup, the survival benefit was observed to be skewed toward patients with high TMB, but it was not statistically significant (OS:HR 0.61, 95% CI 0.32, 1.16, p = 0.133; PFS:HR 0.68, 95% CI 0.31, 1.48, p = 0.322). Conclusions: This meta-analysis demonstrated that gastric cancer patients with high TMB showed significant benefits from ICIs compared to those with low TMB patients, particularly in Asian populations.
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页数:8
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共 64 条
  • [1] Gastric adenocarcinoma
    Ajani, Jaffer A.
    Lee, Jeeyun
    Sano, Takeshi
    Janjigian, Yelena Y.
    Fan, Daiming
    Song, Shumei
    [J]. NATURE REVIEWS DISEASE PRIMERS, 2017, 3
  • [2] Atkins D, 2004, BMJ-BRIT MED J, V328, P1490
  • [3] Bang YJ, 2017, J CLIN ONCOL, V35, DOI 10.1200/JCO.2017.35.15_suppl.4012
  • [4] OPERATING CHARACTERISTICS OF A BANK CORRELATION TEST FOR PUBLICATION BIAS
    BEGG, CB
    MAZUMDAR, M
    [J]. BIOMETRICS, 1994, 50 (04) : 1088 - 1101
  • [5] Mutational landscape of gastric cancer and clinical application of genomic profiling based on target next-generation sequencing
    Cai, Hui
    Jing, Changqing
    Chang, Xusheng
    Ding, Dan
    Han, Ting
    Yang, Junchi
    Lu, Zhengmao
    Hu, Xuguang
    Liu, Zhaorui
    Wang, Jinshen
    Shang, Liang
    Wu, Shouxin
    Meng, Peng
    Lin, Ling
    Zhao, Jiangman
    Nie, Mingming
    Yin, Kai
    [J]. JOURNAL OF TRANSLATIONAL MEDICINE, 2019, 17 (1)
  • [6] Intrahepatic Cholangiocarcinoma: Genomic Heterogeneity Between Eastern and Western Patients
    Cao, Jingyu
    Hu, Jing
    Liu, Siqin
    Meric-Bernstam, Funda
    Abdel-Wahab, Reham
    Xu, Junjie
    Li, Qiang
    Yan, Maolin
    Feng, Yujie
    Lin, Jianzhen
    Zhao, Songhui
    Wang, Jian
    Kwong, Lawrence N.
    Hu, Jinwei
    Carapeto, Fernando
    Borad, Mitesh J.
    Wang, Kai
    Javle, Milind
    Zhao, Haitao
    [J]. JCO PRECISION ONCOLOGY, 2020, 4 : 557 - 569
  • [7] The predictive efficacy of tumor mutation burden in immunotherapy across multiple cancer types: A meta-analysis and bioinformatics analysis
    Cao, Jinlong
    Yang, Xin
    Chen, Siyu
    Wang, Jirong
    Fan, Xinpeng
    Fu, Shengjun
    Yang, Li
    [J]. TRANSLATIONAL ONCOLOGY, 2022, 20
  • [8] Mutational Landscape and Sensitivity to Immune Checkpoint Blockers
    Chabanon, Roman M.
    Pedrero, Marion
    Lefebvre, Celine
    Marabelle, Aurelien
    Soria, Jean-Charles
    Postel-Vinay, Sophie
    [J]. CLINICAL CANCER RESEARCH, 2016, 22 (17) : 4309 - 4321
  • [9] Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden
    Chalmers, Zachary R.
    Connelly, Caitlin F.
    Fabrizio, David
    Gay, Laurie
    Ali, Siraj M.
    Ennis, Riley
    Schrock, Alexa
    Campbell, Brittany
    Shlien, Adam
    Chmielecki, Juliann
    Huang, Franklin
    He, Yuting
    Sun, James
    Tabori, Uri
    Kennedy, Mark
    Lieber, Daniel S.
    Roels, Steven
    White, Jared
    Otto, Geoffrey A.
    Ross, Jeffrey S.
    Garraway, Levi
    Miller, Vincent A.
    Stephens, Phillip J.
    Frampton, Garrett M.
    [J]. GENOME MEDICINE, 2017, 9
  • [10] Development of tumor mutation burden as an immunotherapy biomarker: utility for the oncology clinic
    Chan, T. A.
    Yarchoan, M.
    Jaffee, E.
    Swanton, C.
    Quezada, S. A.
    Stenzinger, A.
    Peters, S.
    [J]. ANNALS OF ONCOLOGY, 2019, 30 (01) : 44 - 56