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. 2023 Oct 6;102(40):e34990. doi: 10.1097/MD.0000000000034990

Table 1.

Characteristics of studies included in the meta-analysis.

Authors Area Experimental Drugs TMB Cutoff Value Detection method Sample size evaluable for TMB Outcomes
Rizvi 2015 America Pembrolizumab 178 WES 34 PFS
Rizvi 2018 America Mono or combo The 50th percentile of TMB Targeted NGS 240 PFS
Hellmann 2018 America Nivolumab plus ipilimumab 158 mutations WES 75 PFS, ORR
Chae 2018 America Anti-PD-1/PD-L1 therapies 15 Targeted NGS 34 PFS, OS
Wang 2019 Asian Anti-PD-1/PD-L1 therapies 6 Targeted NGS 50 PFS, ORR
Ready 2019 America Nivolumab plus low-dose ipilimumab 10 Targeted NGS 98 PFS, ORR
Fang 2019 Asian Anti-PD-(L)1 monotherapy NA Targeted NGS 75 PFS, ORR
Chae 2019 America Anti-PD-1/PD-L1 therapies NA Targeted NGS 20 PFS, OS
Alborelli 2020 Europe Nivolumab/Pembrolizumab/ Atezolizumab/Nivolumab + Ipilimumab 9mut/Mb Targeted NGS 76 PFS, OS
Huang 2020 Asian PD-1/PD-L1 inhibitor monotherapy 10mut/Mb Targeted NGS 34 PFS, OS, ORR

Combo = antiPD-(L)1+anti-cytotoxic T-cell lymphocyte-4 combination therapy, Mono = anti-programmed death 1 or anti-programmed death ligand 1 [anti-PD-(L)1] monotheism, mut = mutation, NA = not available, NGS = next-generation sequencing, ORR = objective response rate, OS = overall survival, PD-1/PD-L1 = programmed death 1/programmed death ligand 1, PFS = progression-free survival, TMB = tumor mutation burden, WES = whole exome sequencing.