Skip to main content
. 2021 Jan 25;12:574. doi: 10.1038/s41467-020-20887-6

Table 4.

Multivariate LASSO analysis.

Type Item All treatments Oxaliplatin containing PLAT/PYR Target-mono TOP/PYR
Clinical Prior Treatment 0.57
Gender 0.77 −1.14 −1.10
Counts nr of Tandem Duplications 1.19
nr of 10kb–1Mb deletions 0.01
Mutational Signatures DBS2 −0.02
DBS5 0.13
DBS11 −0.03
SBS17b 0.07 0.13
SBS39 0.04
SBS41 −0.21
Driver Genes APC 0.23
KRAS 0.78
PIK3CA 0.22
FBXW7 17.65
Non-coding LINC00672 0.90
GISTIC Regions Gain 17q12 (ERBB2*) 0.44
Gain 18p11.32 (CETN1*) 0.59
Gain 20q11.1 (BCL2L1*) 0.12
Gain 8p11.21 (KAT6A) −0.78 −1.56
Gain 7p21.3 (VWDE) 3.68
Gain 7q31.2 (MET*) 3.59
Gain 7p12.3 (PKD1L1) 3.04
Gain 7q34 (no genes in peak) 3.59
Gain 14q23.1 (no genes in peak) 1.64
Loss 18q12.2 (hsa-mir-924*) −1.52 −3.30 2.79
Loss 6q26 (PARK2) −1.38
Loss 9p21.3 (CDKN2A*) −1.88
Loss 16q23.1 (WWOX) −1.70
Loss 4q22.1 (CCSER1) 2.66
Loss 4q35.1 (IRF2) 1.78
Loss 18q21.2 (SMAD4) −1.35 −3.30 2.79
Loss 18q23 (NFATC1*) −1.14 −3.30
Loss Xp22.31 (STS*) −1.40 1.78
Loss 14q23.3 (GPHN) −2.09

Items that reached univariate statistical significance (p < 0.05) were used in a multivariable penalized ordinal regression model for treatment response. Univariate regression was performed for genomic features (Supplementary Data 3) using the ‘polr’ function from the MASS R package (v7.3-51.4) and subsequently those with a univariate two-sided p-value <0.05 were selected for multivariable ordered LASSO regression using the ordinalNet R package (v2.7). Regression coefficients are shown for features that remained significant in the multivariable model.

*Multiple genes present in region; bold: known Fragile Site region