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. 2022 Jan 5;11:780655. doi: 10.3389/fonc.2021.780655

Table 2.

Summary of clinical trials investigating the outcomes of different KRAS co-mutations.

Study Pts KRAS status Treatment Endpoint KRAS status
Skoulidis et al. (110) K-only KP KL ICIs K-only KP KL
174 37% (64) 32% (56) 31% (54) ORR (%) 28.6 35.7 7.4
PFS (months) 2.7 3.0 1.8
OS (months) 16.1 16.0 6.4
Skoulidis et al. (53) KRAS MUT KRAS-KEAP1 MUT Sotorasib KRAS MUT KRAS-KEAP1 MUT
104 81% (84) 19% (20) ORR (%) 44 20
Alessi et al. (111) K-only KS ICIs KS K-only
176 90% (159) 10% (17) ORR (%) 0 22.0
PFS (months) 1.4 4.1
OS (months) 3.0 15.1
Liu et al. (112) K-only KP KS Non-immunotherapy K-only KP KS
155 61% (94) 33% (52) 6% (9) DFS (months) 18.0 16.31 10.97
OS (months) 20.11 18.48 15.37
ICIs
77 56% (43) 32% (25) 12% (9) PFS (months) 2.77 4.63 1.73

KRAS, kirsten rat sarcoma viral oncogene homolog; Pts, patients; KL, KRAS-STK11/LKB1 co-mutant; KP, KRAS-TP53 co-mutant; ORR, objective response rate; PFS, progression-free survival; OS, overall survival; MUT, mutation; KEAP1, Kelch-like ECH-associated protein 1; ICIs, immune checkpoint inhibitors; KS, KRAS-SMARCA4 co-mutant; DFS, disease-free survival.