Table 1.
First author | Platform/genes analyzed | N of patients | Genomic alterations (%) |
---|---|---|---|
Nakamura et al. (13) | WES | 260 | ICC: KRAS 25%, FGFR2 8%, IDH1 6%; EHC: TP53 26%, KRAS 12%, SMAD4 10%; GBC: TP53 43%, ARID2 18%, EGFR 18% |
Javle et al. (14) | HC NGS 182 | ICC 412; EHC 57; GBC 85 | ICC: TP53 27%, KRAS 22%, IDH1 16%; EHC: KRAS 42%, TP53 40%, SMAD4 21 %; GBC: TP53 59%, CDKN2A/B 19%, ERBB2 16% |
Lowery et al. (15) | HC NGS 341/410 | ICC 158; EHC 37 | ICC: IDH1 30%, BAP1 20%, FGFR2 14%; EHC: KRAS 38%, TP53 49%, SMAD4 30% |
Narayan et al. (16) | HC NGS 341/410 | GBC 81 | TP53 58%, SMAD4 31%, ARID1A 25% |
Churi et al. (17) | AB NGS 46 | ICC 55; EHC 20 | ICC: TP53 29%, KRAS 24%, IDH 24%; EHC: KRAS 40%, TP53 45%, SMAD4 25% |
Li et al. (18) | WES | GBC 57 | TP53 47%, ERBB3 12%, KRAS 8% |
Ross et al. (19) | HC NGS 182 | ICC 28 | ARID1A 36%, IDH1/2 36%, TP53 36% |
Zou et al. (20) | WES | ICC 102 | TP53 38%, KRAS 17%, ARID1A 7% |
WES, whole-exome sequencing; HC NGS, hybrid capture next generation sequencing; AB NGS, amplicon-based next generation sequencing; ICC, intrahepatic cholangiocarcinoma; EHC, extrahepatic cholangiocarcinoma; GBC, gallbladder cancer.