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. 2024 Feb 13;78(3):e209341. doi: 10.1136/jcp-2023-209341

Table 2. Clinical and molecular characteristics of GI malignancies exhibiting MTAP loss as compared with MTAP unaltered GI tumours from the TCGA PanCancer Atlas Studies.

MTAP loss MTAP unaltered P value
No of patients 128 1224
Median age (IQR) 63 (56–72) 66 (57–74) 0.151
Sex (%) 0.039
 Male 89 (69.5) 730 (59.6)
 Female 39 (30.5) 462 (40.2)
 NA 0 (0.0) 2 (0.2)
Cancer type (%) <0.001
 Gastro-oesophageal 78 (60.9) 534 (43.6)
 Pancreatic 40 (31.3) 138 (11.3)
 Colorectal 6 (4.7) 520 (42.5)
 Biliary 4 (3.1) 32 (2.6)
Tumour histology (%) <0.001
 Adenocarcinoma 95 (74.2) 1002 (81.9)
 Mucinous adenocarcinoma 2 (1.6) 75 (6.1)
 Signet ring carcinoma 4 (3.1) 80 (6.5)
 Squamous carcinoma 27 (21.1) 67 (5.5)
Stage at diagnosis (%) 0.495
 Non metastatic 82 (64.1) 931 (76.1)
 Metastatic 12 (9.4) 103 (8.4)
 NA 34 (36.2) 190 (15.5)
Tumour mutational burden* (median (IQR)) 2.5 (1.6–4.1) 3.3 (2.07–5.3) <0.001
Microsatellite instability (%) 1 (0.8) 164 (13.4) <0.001
CDKN2A/B loss (%) 125 (97.7) 57 (8.1) <0.001
TP53 mutant (%) 84 (65.6) 703 (57.4) 0.044
KRAS mutant (%) 41 (32.0) 332 (27.1) 0.253
BRAF V600E mutant (%) 1 (0.8) 48 (3.9) 0.080
APC mutant (%) 6 (7.1) 435 (35.5) <0.001
ERBB2 amplification 21 (16.4) 92 (7.5) 0.001
*

Nonsynonymous TMB.

According to the MANTIS score with a threshold of 0.4.

GIgastrointestinalMANTISMicrosatellite Analysis for Normal-Tumor InStabilityNAnot availableTCGAThe Cancer Genome AtlasTMBTumour mutational burden