TABLE 3.
Study | Design | GBM | IMT | Predictor | Outcomes |
---|---|---|---|---|---|
Patient clinical characteristics | |||||
Ishikawa et al. (2014) 43 | Phase I/IIa | nGBM | Vaccine | RPA (III/IV vs. V) | OS |
Ardon et al. (2012) 31 | Phase I/II | nGBM | DCs | RPA | OS, PFS |
Narita et al. (2019) 48 | Phase III | rGBM | Vaccine | age (≥70 vs. <70 years old), weight (≥70 vs. <70 kg), PS (0–2 vs. 3) | OS |
Tumor mutational burden and signatures | |||||
Bouffet et al. (2016) 91 | Case report | rGBM | ICI | germline bMMRD with hypermutation | response |
Johanns et al. (2016) 92 | Case report | rGBM | ICI | germline POLE alteration with hypermutation | response |
AlHarbi et al. (2018) 93 | Case report | rGBM | ICI | constitutional bMMRD | response |
Gromeier et al. (2021) 94 | Retrospective | rGBM | ICI, OV | tumor mutational burden | OS |
Zhao et al. (2019) 95 | Retrospective | rGBM | ICI | MAPK pathway alterations (PTPN11, BRAF); PTEN mutation | response |
Yao et al. (2018) | Phase II | both | DCs | TERT mutation | OS, PFS |
Tumor molecular characteristics | |||||
Arrieta et al. (2021) 108 | Retrospective | rGBM | ICI | ERK1/2 phosphorylation | OS |
Ishikawa et al. (2007) 101 | pilot clinical trials | both | vaccine | p53 and MHC‐1 expression | response |
Liau et al. (2005) 102 | Phase I | both | DCs | TGF‐2 expression | OS |
Yao et al. (2018) 66 | Phase II | both | DCs | B7‐H4 protein expression | OS |
Duerinck et al. (2021) 100 | Phase I | rGBM | ICI | B7‐H3 mRNA expression | OS |
Chiba et al. (2010) 103 | Retrospective | rGBM | Vaccine | intermediate WT1 expression | OS, PFS |
Phuphanich et al. (2013) 52 | Phase I | nGBM | Vaccine | mRNA expression of vaccine‐targeted tumor antigen | OS, PFS |
Prins et al. (2011) 107 | Phase I | both | DCs | mesenchymal gene expression profile | OS |
Tumor‐infiltrating lymphocytes | |||||
Jan et al. (2018) 45 | Phase II | nGBM | DCs | low PD‐1+/CD8+ ratio on TILs and PBMCs; low PD‐l + TILs | OS, PFS |
Zhang et al. (2020) 115 | Retrospective | nGBM | Vaccine | low TCR repertoire diversity; TCR clones of TILs; | OS |
Hsu et al. (2016) 114 | Retrospective | both | DCs | higher estimated TIL content | OS, PFS |
Patient peripheral blood | |||||
Lukas et al. (2018) 46 | Phase I | rGBM | ICI | high baseline peripheral CD4+ T cells and B cells | OS, PFS |
Erhart et al. (2018) 116 | Phase II | nGBM | DCs | GranzB production; CD8+ T cells counts | OS |
Bloch et al. (2017) 34 | Phase II | nGBM | Vaccine | PD‐L1 expression on myeloid cells | OS, PFS |
Narita et al. (2019) 48 | Phase III | rGBM | Vaccine | CD11b + CD14 + HLA‐DRlow monocytes; CCL2 in plasma; CD3 + CD4 + CD45RA − T cells | OS |
Takashima et al. (2016) 61 | Phase II | rGBM | Vaccine | low SDC‐4 mRNA expression levels of PBMCs | OS |
Abbreviations: bMMRD, biallelic mismatch repair deficiency; DCs, dendric cells; GBM, glioblastoma; ICI, immune checkpoint inhibitor; IMT, immunotherapy; nGBM, newly diagnosed GBM; OS, overall survival; OV, oncolytic virus; PBMCs, peripheral blood mononuclear cells; PD‐1, programmed cell death protein 1; PD‐L1, programmed death‐ligand 1; PFS, progression‐free survival; rGBM, recurrent GBM; RPA, recursive partitioning analysis; TCR, T‐cell receptor; TILs, tumor‐infiltrating lymphocytes; WT1, Wilms' tumor 1.