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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 3.

Association between RSPO2 rs555008 and clinical outcomes among mCRC patients according to RAS 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
RAS wild-type

Training cohort T/T 94 51(62.2%) 31(37.8%) 0.34 9.9(8.8,12.0) Reference 0.073 Reference 0.25 23.6(18.6,27.5) Reference 0.009 Reference 0.16
Any G 73 48(69.6%) 21(30.4%) 11.5(9.3,12.9) 0.74(0.53,1.04) 0.81(0.56,1.16) 29.0(24.2,39.5) 0.60(0.41,0.89) 0.74(0.48,1.13)

Validation cohort T/T 24 14(58.3%) 10(41.7%) 0.67 9.0(6.7,11.7) Reference 0.31 Reference 0.53 19.4(11.2,26.3) Reference 0.021 Reference 0.11
Any G 25 12(52.2%) 11(47.8%) 11.3(7.7,12.7) 0.72(0.38,1.39) 0.78(0.36,1.70) 37.8(20.8,52.5) 0.49(0.25,0.94) 0.53(0.24,1.16)

Control cohort T/T 86 57(80.3%) 14(19.7%) 0.39 10.4(9.2,13.0) Reference 0.90 Reference 0.69 37.1(21.9,41.2) Reference 0.62 Reference 0.49
Any G 93 61(74.4%) 21(25.6%) 10.6(8.7,12.8) 1.02(0.74,1.41) 1.07(0.76,1.50) 29.8(23.7,40.0) 1.11(0.74,1.66) 1.16(0.76,1.78)

RAS mutant

Training cohort T/T 43 22(52.4%) 20(47.6%) 0.82 10.9(8.5,13.0) Reference 0.11 Reference 0.020 21.3(15.9,31.5) Reference 0.52 Reference 0.074
Any G 32 16(55.2%) 13(44.8%) 9.2(7.2,13.4) 1.47(0.87,2.48) 2.01(1.12,3.62) 19.0(16.3,26.9) 1.19(0.70,2.01) 1.81(0.94,3.45)

Validation cohort T/T 74 41(56.9%) 31(43.1%) 0.89 9.5(8.6,11.8) Reference 0.042 Reference 0.18 25.6(20.8,37.2) Reference 0.20 Reference 0.75
Any G 36 21(58.3%) 15(41.7%) 9.2(7.8,9.9) 1.57(0.98,2.50) 1.40(0.86,2.29) 20.8(17.8,27.9) 1.33(0.85,2.10) 0.92(0.56,1.52)
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.