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. 2020 Nov 22;21(22):8841. doi: 10.3390/ijms21228841

Table 1.

Genetic status in canonical driver genes, overall incidence, and prognosis of each pancreatic cancer variants.

Subtype KRAS TP53 SMAD4 CDKN2A Incidence Prognosis Ref
CC 30–50% 20% n.a. n.a. 1–3% Good (5-year survival >55%) [9,10,11,12]
Medullary carcinoma 17–30% 18% n.a. n.a. <1% Still unclear [13,14,15,16]
ASC 90–100% 50–90% 18->90% 6% 1–4% Poor (9 months from the diagnosis) [17,18,19,20,21,22,23]
UDC 30–70% 30–60% n.a. n.a. <1% Extremely poor (5 months from the diagnosis [24,25,26,27,28,29]
UCOGC 70–100% 50–100% 10–50% 25% <1% Better than UDC [24,25,26,27,30,31,32,33,34,35,36]
Rhabdoid carcinoma 40% 40–50% n.a. n.a. <1% Still unclear [37]
Hepatoid carcinoma n.a. n.a. n.a. n.a. <1% Still unclear [38,39]
SRCC n.a. n.a. n.a. n.a. <1% Poor [40,41]

ASC, adenosquamous carcinoma; CC, colloid carcinoma; n.a., not assessed; SRCC, signet-ring cell carcinoma; UCOGC, undifferentiated carcinoma with osteoclast-like giant cells; UDC, undifferentiated carcinoma.