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. 2020 Nov 13;10:587692. doi: 10.3389/fonc.2020.587692

Table 2.

Univariate analysis of PFS and OS in 46 patients.

Variables PFS OS
Univariate analysis Univariate analysis
HR (95% CI) P HR (95% CI) P
Age (years)
 <60 Ref. Ref.
 ≥60 1.362 (0.734–2.527) 0.328 1.036 (0.486–2.210) 0.926
Gender
 Male Ref. Ref.
 Female 1.048 (0.556–1.974) 0.886 1.273 (0.589–2.752) 0.540
ECOG PS
 0–1 Ref. Ref.
 2 1.240 (0.377–4.081) 0.723 1.061 (0.251–4.491) 0.936
Primary site
 Colon Ref. Ref.
 Rectum 0.509 (0.168–1.541) 0.232 0.875 (0.333–2.305) 0.788
 Unknown 0.615 (0.163–2.325) 0.474 0.668 (0.207–2.157) 0.500
Metastatic organs
 1–2 Ref. Ref.
 ≥3 1.703 (0.886–3.275) 0.110 1.993 (0.134–7.376) 0.398
RAS mutant
 Yes Ref. Ref.
 No 1.225 (0.518–2.896) 0.644 1.494 (0.494–4.519) 0.477
 Unknown 1.805 (0.690–4.723) 0.229 1.867 (0.559–6.232) 0.310
Lines of previous therapy
 2 Ref. Ref.
 ≥3 1.187 (0.589–2.392) 0.631 1.830 (0.691–4.844) 0.188
Previous Bevacizumab
 Yes Ref. Ref.
 No 1.017 (0.446–2.319) 0.968 2.659 (0.997–7.091) 0.051
Previous anti-VEGFR
 Yes Ref. Ref.
 No 2.423 (1.245–4.715) 0.009 1.004 (0.438–2.303) 0.992
Sufficient Treatment*
 Yes Ref. Ref.
 No 1.093 (0.584–2.045) 0.782 1.236 (0.577–2.650) 0.586
NLR
 ≤3 Ref. Ref.
 >3 1.976 (1.061–3.682) 0.032 2.332 (1.085–5.011) 0.030
PLR
 >300 Ref. Ref.
 150–300 0.659 (0.283–1.534) 0.333 1.122 (0.425–2.962) 0.816
 <150 0.570 (0.234–1.385) 0.214 0.396 (0.137–1.147) 0.088
CEA
 ≤5 Ref. Ref.
 >5 1.308 (0.506–3.382) 0.579 1.072 (0.321–3.577) 0.910
Hand-foot syndrome
 Yes Ref. Ref.
 No 2.153 (1.077–4.304) 0.030 1.262 (0.565–2.814) 0.570
Hypertension
 Yes Ref. Ref.
 No 1.796 (0.869–1.796) 0.114 1.291 (0.545–3.060) 0.562
Fatigue
 Yes Ref. Ref.
 No 1.128 (0.544–2.340) 0.746 1.987 (0.750–5.264) 0.167

PFS, progression-free survival; OS, overall survival; HR, hazard ratio; CI, confidence interval; ECOG PS, Eastern Cooperative Oncology Group performance status; VEGFR, vascular endothelial growth factor receptor; NLR, neutrophil-to-lymphocyte ratio; PLR, platelet-to-lymphocyte ratio, CEA, carcinoembryonic antigen.

*Fruquintinib was administered without dose reduction, treatment interruption, or therapy discontinuation.