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. 2023 Jul 26;29(19):3892–3900. doi: 10.1158/1078-0432.CCR-23-0926

Table 1.

Characteristics of the EORTC-26101 clinical study and biomarker cohort.

EORTC-26101 study cohort EORTC-26101 biomarker cohort P value
N (%) 596 (100) 380 (63.8)
Sex
 Female 223 (37.4) 153 (40.3) 0.38
 Male 373 (62.6) 227 (59.7)
OS [median (95% CI)] 8.9 (8.3–9.6) 9.2 (8.4–10.0) 0.57
PFS [median (95% CI)] 2.9 (2.8–3.0) 2.9 (2.8–3.4) 0.48
Age [mean ± SD] 56.8 ± 10.7 57.0 ± 10.7 0.76
Steroid use
 yes 295 (49.5) 181 (47.6) 0.60
 no 301 (50.5) 199 (52.4)
ECOG performance status
 0 204 (34.2) 139 (36.6) 0.49
 >0 392 (65.8) 241 (63.4)
Tumor diameter
 Equal or smaller than 40 mm 323 (54.2) 210 (55.3) 0.79
 Larger than 40 mm 273 (45.8) 170 (44.7)
Origin of tissue for molecular analysis
 Primary tumor NA* 245 (64.5) NA*
 Progressive tumor 2 (0.5)
 No information available 133 (35.0)
Treatment
 Lomustine 149 (25.0) 99 (26.1) 0.87
 Lomustine + bevacizumab 288 (48.3) 189 (49.7)
 Sequence 159 (26.7) 92 (24.2)
MGMT
 Methylated NA* 167 (43.9) NA*
 Unmethylated 146 (38.4)
 Not determinable 67 (17.6)
IDH
 Wild-type NA* 370 (97.4) NA*
 Mutated 10 (2.6)

Clinical characteristics did not differ significantly between the clinical study and biomarker cohort. *NA, not available; inherent discrepancy between the whole cohort, which contains patients with and without biomarker data available, and the biomarker cohort.

Abbreviation: ECOG, Eastern Cooperative Oncology Group.