Table 1 Overview of data sets used in this study.

From: Very low mutation burden is a feature of inflamed recurrent glioblastomas responsive to cancer immunotherapy

 

Immunotherapy-treated cohorts

Comparison cohorts

Cohort:

PVSRIPO rGBM

Anti-PD1/PD-L1 GBM

TCGA pGBM

GLASS rGBM

Wang rGBM

Reference:

Desjardins et al.1

Samstein et al.8

Zhao et al.10

N/A

Barthel et al.11

Wang et al.16

Information used for this study

Survival, TMB, RNAseq

Survival, TMB

Survival, TMB, RNAseq

Survival, TMB, RNAseq

Survival, TMB,

Survival, TMB, RNAseq

Comparison

n

Fig.

n

Fig.

n

Fig.

n

Fig.

n

Fig.

n

Fig.

Pre-Tx TMB vs. survival

21

1a, S1

81

1c

29

1d

277

1e

132

1f

 IDH1 wt

19

1b

76

1c

21

1d

 Exclude MGMT meth:

14

S2a

 IDH1 wt; no MGMT meth:

13

S2b

 PTEN wt only:

17

S2j

TTR vs. survival

45

1b

131a

1g

 IDH1 wt:

35

S2d

 Exclude MGMT meth:

28

S2e

  IDH1 wt; no MGMT meth:

22

S2f

TP53 mut vs. survival:

34

S2c

 IDH1 wt:

31

S2g

 Exclude MGMT meth:

22

S2h

 IDH1 wt; no MGMT meth:

21

S2i

Steroids vs. survival (TMB cohort):

21

S2k

Steroids vs. survival (TTR cohort):

45

S2j

Inflammatory gene sets vs. TMB:

14

2b, S4-6

11

2b, S5,6

193

2, S5,6

25

2b, S5,6

 Immunoediting vs. TMB:

18b

2c

115c

2d

 Paired pGBM vs. rGBM

25

2e/f, S8

  1. Tx treatment, TTR time to first recurrence, meth methylation.
  2. aOnly tumors tested at first recurrence.
  3. bTumors sequenced on the same WES panel.
  4. cNeoantigen (neo-Ag) ratios available from a subset of the cohort.