Table 1.
Study Set | No. of Patients | No. with Matched DNA from Non-neoplastic Tissue | Sex | Age(yr) | Vital Status | Median Weeks of Follow-up (Range) | Data Type† | Source |
---|---|---|---|---|---|---|---|---|
1 | 219‡ | 91 | Female: 77 Male: 130 |
55.8±15.1 | Dead: 192 Alive: 15 |
50.6 (1.1–503.4) | G, E, C | Cancer Genome Atlas Project |
2 | 182 | 0 | NA | NA | NA | NA | G | REMBRANDT release 1.5.4.1 |
3 | 46 | 0 | NA | NA | NA | NA | G | REMBRANDT release 1.5.3 |
4 | 36 | 0 | NA | NA | NA | NA | G | Northwestern University |
5 | 32 | 0 | NA | NA | NA | NA | S | Stanford University |
6 | 15 | 0 | NA | NA | NA | NA | S | Barrow Neurological Institute |
7 | 49§ | 0 | Female: 15 Male: 34 |
49.9±12.1 | Dead: 46 Alive: 3 |
70.0 (3.0–313.0) | E, C | M.D. Anderson Cancer Center (GEO accession no., GSE4271) |
8 | 47 | 0 | Female: 25 Male: 22 |
50.5±15.6 | Dead: 34 Alive: 13 |
42.0 (1.0–178.0) | E, C | University of California, Los Angeles (GEO accession no., GSE4412) |
9 | 191 | 0 | Female: 74 Male: 117 |
53.8±13.6 | Dead: 176 Alive: 15 |
55.6 (1.0–479.0) | E, C | Multi-institutional (GEO accession no., GSE13041) |
10 | 76 | 0 | Female: 21 Male: 55 |
51.1±9.1 | Dead: 63 Alive: 13 |
66.9 (6.1–311.9) | E, M, C | Phase 2 trial, EORTC-NCIC phase 3 trial (GEO accession no., GSE7696)¶ |
Plus–minus values are means ± SD. GEO denotes Gene Expression Omnibus, and NA not available.
The types of data include clinical-outcome data (C), gene-expression data (E), gene copy number data (G), methylation status of the MGMT promoter (M), and sequencing data (S).
There were 219 patients in study set 1; clinical data were available for 207 of those patients.
Twenty-two patients had matched tumor pairs from the initial diagnosis and recurrent disease; therefore, 71 tumors were assessed in study set 7.
Study set 10 included 76 patients with glioblastoma who were treated as part of a phase 2 trial or a European Organization for Research and Treatment of Cancer (EORTC)/National Cancer Institute of Canada (NCIC) randomized phase 3 trial (22981-26981/CE.38), both of which evaluated the addition of concomitant and adjuvant temozolomide to radiotherapy.31,32