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. 2021 Mar 22;123(8):1773–1783. doi: 10.1002/jso.26466

Table 2.

Clinical risk score, metabolic characteristics and metabolic clinical risk score in DHGP and non‐DHGP groups

DHGP (n = 22) Non‐DHGP (n = 86) P value
KRAS mutation 9 (47.4%) 33 (42.9%) 0.799
Clinical risk score, n (%) 0.585
0 1 (4.5%) 3 (3.5%)
1 2 (9.1%) 13 (15.1%)
2 8 (36.4%) 30 (34.9%)
3 7 (31.8%) 31 (36%)
4 4 (18.2%) 6 (7%)
5 0 3 (3.5%)
High risk clinical risk score, n (%) 11 (50%) 40 (46.5%) 0.814
SUVmax/SUVmean(liver) 3.16 (1.74) 4.26 (2.5) 0.009
SUVmax/SUVmean(liver) > 4.3 3 (13.6%) 43 (50%) 0.003
Metabolic clinical risk score 0.94
0 1 (4.5%) 3 (3.5%)
1 2 (9.1%) 8 (9.3%)
2 7 (31.8%) 19 (22.1%)
3 7 (31.8%) 33 (38.4%)
4 4 (18.2%) 15 (17.4%)
5 1 (4.5%) 5 (5.8%)
6 0 3 (3.5%)
High risk metabolic clinical risk score 5 (22.7%) 23 (26.7%) 0.791
Neoadjuvant chemotherapy 19 (86.4%) 66 (76.7%) 0.396
Immunotherapy 0.835
Bevacizumab 2 (9.1%) 8 (9.3%)
Cetuximab 3 (13.6%) 8 (9.3%)