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. Author manuscript; available in PMC: 2018 Aug 1.
Published in final edited form as: Gut. 2016 May 5;66(8):1463–1473. doi: 10.1136/gutjnl-2016-311421

Table 5.

Tumour CD274 expression and colorectal cancer patient mortality

Tumour CD274 expression score Total No. Colorectal cancer-specific mortality
Overall mortality
No. of events Univariable HR (95% CI) Multivariable HR (95% CI)* No. of events Univariable HR (95% CI) Multivariable HR (95% CI)*
0 91 24 1 (reference) 1 (reference) 47 1 (reference) 1 (reference)
1 230 70 1.18 (0.74–1.87) 1.00 (0.63–1.60) 121 1.00 (0.71–1.40) 0.89 (0.63–1.25)
2 216 61 1.10 (0.68–1.76) 1.00 (0.62–1.60) 117 1.08 (0.77–1.51) 1.02 (0.72–1.43)
3 235 79 1.28 (0.81–2.03) 0.95 (0.60–1.52) 139 1.06 (0.76–1.48) 0.96 (0.68–1.34)
4 43 12 1.06 (0.53–2.12) 0.64 (0.32–1.28) 26 1.03 (0.64–1.66) 0.73 (0.45–1.19)
Ptrend 0.49 0.30 0.65 0.66

Abbreviations: CI, confidence interval; HR, hazard risk.

*

The multivariable Cox regression model initially included age, sex, year of diagnosis, family history of colorectal carcinoma in any parent or sibling, tumour location, disease stage, microsatellite instability, CpG island methylator phenotype, KRAS, BRAF, and PIK3CA mutations, and LINE-1 methylation level. A backward stepwise elimination with a threshold of P=0.05 was used to select variables in the final models.

Ptrend value was calculated across the ordinal categories of tumour CD274 expression score as a continuous variable in the Cox regression model.

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