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

Table 2.

Univariate and multivariate analysis for progression‐free survival

Category Univariate Multivariate
HR (95% CI) p valuea HR (95% CI) p valuea
KRAS exon 2 mutation: G12C vs. non‐G12C 1.47 (1.08–2.01) .015 1.43 (1.04–1.96) .030
Age: ≥65 vs. <65 years 0.97 (0.83–1.14) .724
Gender: Male vs. female 0.98 (0.83–1.15) .794
ECOG PS: 1 or 2 vs. 0 1.48 (1.24–1.78) <.001 1.08 (0.88–1.33) .443
Primary tumor site: left vs. right 0.93 (0.79–1.10) .417
Surgery on primary tumor: Yes vs. No 0.69 (0.59–0.81) <.001 0.82 (0.69–0.99) .035
Time of first metastasis: Synchronous vs. metachronous 1.15 (0.97–1.35) .113
Histology: Poor/muc vs. well/mod 1.17 (0.89–1.54) .258
Serum LDH, IU/L: ≥210 (median) vs. <210 1.50 (1.28–1.76) <.001 1.24 (1.04–1.47) .014
GPS: 1 or 2 vs. 0 1.96 (1.58–2.44) <.001 1.53 (1.21–1.93) <.001
Number of metastatic organ sites: ≥2 vs. 1 1.46 (1.25–1.71) <.001 1.32 (1.12–1.55) .001
First‐line backbone regimen: Doubletb or tripletc vs. monod 0.84 (0.57–1.22) .355
First‐line bevacizumab: Yes vs. no 0.51 (0.42–0.63) <.001 0.57 (0.45–0.71) <.001
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.