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. 2022 Nov 15;12(11):5300–5314.

Table 2.

Univariate Cox regression analyses of clinical pathological variables against PFS and OS in the TCGA cohort with 33 KRAS-mutated MSS CRC patients

Characteristics Number of patients PFS OS


Number of events HR, 95% CI P-value Number of events HR, 95% CI P-value
Pathology subtype
    COAD 24 17 ref 14 ref
    READ 9 4 0.45 [0.15-1.35] 0.155 1 0.14 [0.02-1.07] 0.058
Molecular subtype
    CIN 28 18 ref 13 ref
    GS 2 1 0.72 [0.1-5.42] 0.748 1 1.42 [0.18-11.05] 0.738
Sex
    Female 16 8 ref 6 ref
    Male 17 13 0.87 [0.36-2.11] 0.754 9 0.99 [0.35-2.8] 0.985
pN
    N0 3 2 ref 2 ref
    N1 13 8 0.68 [0.14-3.24] 0.627 5 0.34 [0.06-1.82] 0.209
    N2 17 11 0.85 [0.19-3.86] 0.829 8 0.52 [0.11-2.49] 0.413
pM
    MX 3 1 ref 0 ref
    M1 30 20 3.26 [0.44-24.39] 0.250 15 \
Age 33 21 1.01 [0.97-1.05] 0.647 15 1.09 [1.02-1.16] 0.010

COAD: Colon Adenocarcinoma; READ: Rectum Adenocarcinoma; CIN: Chromosomal Instability; GS: Genomic Stable; MSS: Microsatellite Stable; CRC: Colorectal Cancer; TCGA: The Cancer Genome Atlas; PFS: Progression-Free Survival; OS: Overall Survival.