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. 2021 Jul 7;26(10):845–853. doi: 10.1002/onco.13870

Table 3.

Univariate and multivariate analysis for overall survival

Category Univariate Multivariate
HR (95% CI) p valuea HR (95% CI) p valuea
KRAS exon 2 mutation: G12C vs. non‐G12C 1.50 (1.08–2.08) .015 1.42 (1.01–2.00) .044
Age: ≥65 vs. <65 years 1.03 (0.87–1.22) .725
Gender: Male vs. female 0.90 (0.76–1.07) .219
ECOG PS: 1 or 2 vs. 0 1.78 (1.46–2.17) <.001 1.25 (1.00–1.57) .049
Primary tumor site: left vs. right 0.82 (0.68–0.98) .028 0.99 (0.82–1.21) .976
Surgery on primary tumor: Yes vs. no 0.58 (0.48–0.69) <.001 0.75 (0.60–0.93) .010
Time of first metastasis: Synchronous vs. metachronous 1.47 (1.23–1.77) <.001 0.95 (0.76–1.19) .647
Histology: por/muc vs. well/mod 1.44 (1.07–1.94) .016 1.44 (1.06–1.95) .021
Serum LDH, IU/L: ≥210 (median) vs. <210 1.93 (1.62–2.30) <.001 1.59 (1.31–1.92) <.001
GPS: 1 or 2 vs. 0 2.31 (1.83–2.90) <.001 1.64 (1.27–2.12) <.001
Number of metastatic organ site: ≥2 vs. 1 1.63 (1.37–1.94) <.001 1.45 (1.21–1.74) <.001
First‐line backbone regimen: Doubletb or tripletc vs. monod 0.60 (0.41–0.90) .012 0.76 (0.50–1.17) .219
First‐line bevacizumab: Yes vs. no 0.69 (0.55–0.86) <.001 0.84 (0.66–1.08) .174
a

Values of p were calculated using the Cox proportional hazard model.

b

Doublet indicates oxaliplatin‐based regimens (FOLFOX, CAPOX, and SOX) or irinotecan‐based regimens (FOLFIRI, IRIS [SIRB], CAPIRI).

c

Triplet indicates FOLFOXIRI.

d

Mono indicates 5‐fluorouracil (5‐FU)/leucovorin (LV), capecitabine, tegafur‐uracil (UFT)/LV, or S‐1 monotherapy.

Abbreviations: CI, confidence interval; ECOG PS, Eastern Cooperative Oncology Group performance status; GPS, Glasgow prognostic score; HR, hazard ratio; KRAS, Kirsten rat sarcoma; LDH, lactate dehydrogenase; mod, moderately differentiated; muc, mucinous adenocarcinoma; poor, poorly differentiated; well, well differentiated.