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. Author manuscript; available in PMC: 2020 Sep 24.
Published in final edited form as: Eur J Cancer. 2020 Apr 16;131:89–97. doi: 10.1016/j.ejca.2020.02.048

Table 2.

Association between RSPO2 rs555008 and clinical outcomes among mCRC patients according to KRAS status

Tumor response Progression-free survival Overall survival

Genotype N Yes No Chi- square test P value Median (95%CI), months HR (95%CI) Log-rank test P value Adjusted HR (95%CI) a Wald test P value Median (95%CI), months HR (95%CI) Log-rank test P value Adjusted HR (95%CI) a Wald test P value
KRAS wild-type

Training cohort T/T 121 69(63.3%) 40(36.7%) 0.44 10.1(9.0,12.0) Reference 0.16 Reference 0.44 22.3(17.5,26.4) Reference 0.011 Reference 0.15
Any G 91 57(68.7%) 26(31.3%) 11.5(9.6,13.0) 0.81(0.59,1.09) 0.88(0.64,1.22) 28.4(22.7,35.0) 0.64(0.45,0.90) 0.76(0.52,1.11)

Validation cohort T/T 48 29(61.7%) 18(38.3%) 0.64 9.0(7.6,11.0) Reference 0.17 Reference 0.29 23.3(14.6,26.9) Reference 0.046 Reference 0.012
Any G 38 24(66.7%) 12(33.3%) 11.6(9.9,12.7) 0.72(0.44,1.17) 0.74(0.43,1.28) 36.0(23.9,48.7) 0.62(0.38,1.00) 0.49(0.28,0.86)

Control cohort T/T 105 65(75.6%) 21(24.4%) 0.42 10.1(8.5,11.3) Reference 0.74 Reference 0.66 36.4(21.9,39.4) Reference 0.46 Reference 0.46
Any G 121 76(70.4%) 32(29.6%) 10.0(8.3,12.2) 1.05(0.79,1.40) 1.07(0.80,1.43) 27.6(22.5,33.8) 1.14(0.80,1.63) 1.15(0.80,1.65)

KRAS mutant

Training cohort T/T 23 9(40.9%) 13(59.1%) 0.45 11.2(8.3,14.7) Reference 0.023 Reference 0.099 26.3(18.2,36.0) Reference 0.076 Reference 0.057
Any G 19 10(52.6%) 9(47.4%) 8.1(6.1,12.3) 1.93(0.98,3.79) 1.98(0.88,4.45) 16.5(12.5,25.1) 1.75(0.91,3.36) 2.58(0.97,6.87)

Validation cohort T/T 60 33(55.9%) 26(44.1%) 0.60 10.3(8.8,13.0) Reference 0.009 Reference 0.027 27.9(20.8,38.3) Reference 0.10 Reference 0.59
Any G 28 14(50.0%) 14(50.0%) 8.7(7.8,9.5) 1.91(1.12,3.28) 1.99(1.08,3.65) 19.8(15.6,26.3) 1.52(0.91,2.56) 1.17(0.66,2.06)
a

Based on the multivariable Cox proportional hazards regression model adjusting for sex, age, ECOG performance status, primary tumor site, liver limited metastases, primary tumor resection, adjuvant chemotherapy, and BRAF status in the training and control cohorts; adjusting for sex, age, ECOG performance status, primary tumor site, number of metastatic sites, primary tumor resection, and BRAF status in the validation set.