Table 2.
Cox regression – hazard ratios of discontinuation due to inefficacy, to adverse events, and to any reason
Number of subjects=502
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---|---|---|---|---|---|---|---|---|---|
Number of observed treatment period=1026
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Standard error adjusted for individual clusters
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Variables | Discontinuation due to inefficacy
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Discontinuation due to adverse events
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Discontinuation due to any reason
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HR | Standard error | p-Value | HR | Standard error | p-Value | HR | Standard error | p-Value | |
Order of treatment | 1.272 | 0.087 | <0.001 | 1.349 | 0.128 | 0.002 | 1.260 | 0.070 | <0.001 |
Age | 1.007 | 0.004 | 0.066 | 1.006 | 0.006 | 0.361 | 1.007 | 0.003 | 0.015 |
Male | 0.898 | 0.153 | 0.528 | 0.620 | 0.142 | 0.036 | 0.769 | 0.097 | 0.037 |
RF | 1.048 | 0.138 | 0.725 | 0.900 | 0.154 | 0.536 | 1.003 | 0.094 | 0.973 |
Anti-CCP | 0.878 | 0.115 | 0.317 | 0.914 | 0.158 | 0.601 | 0.898 | 0.085 | 0.257 |
Steroid | 0.931 | 0.108 | 0.537 | 1.112 | 0.183 | 0.519 | 0.985 | 0.084 | 0.856 |
sDMARD | 0.818 | 0.121 | 0.175 | 0.585 | 0.127 | 0.014 | 0.707 | 0.077 | 0.001 |
Years of disease | 1.000 | 0.006 | 0.972 | 1.015 | 0.007 | 0.037 | 1.006 | 0.004 | 0.109 |
Gap above 30 days | 0.604 | 0.116 | 0.009 | 0.829 | 0.207 | 0.454 | 0.730 | 0.088 | 0.009 |
Biological | |||||||||
ETA | 1.220 | 0.444 | 0.584 | 0.630 | 0.261 | 0.265 | 0.767 | 0.181 | 0.26 |
ADA | 1.772 | 0.633 | 0.109 | 0.554 | 0.228 | 0.152 | 0.976 | 0.225 | 0.916 |
RTX | 0.450 | 0.172 | 0.036 | 0.505 | 0.234 | 0.139 | 0.434 | 0.108 | 0.001 |
INF | 1.552 | 0.565 | 0.227 | 1.040 | 0.416 | 0.923 | 1.088 | 0.256 | 0.72 |
TCZ | 0.597 | 0.257 | 0.23 | 0.474 | 0.246 | 0.151 | 0.455 | 0.137 | 0.009 |
GOL | 0.942 | 0.392 | 0.886 | 0.918 | 0.426 | 0.854 | 0.746 | 0.209 | 0.295 |
Note: Bold: significant at 0.05 level.
Abbreviations: ADA, adalimumab; CCP, cyclic citrullinated peptide; ETA, etanercept; GOL, golimumab; HR, hazard ratio; INF, infliximab; RF, rheumatoid factor; RTX, rituximab; sDMARD, synthetic disease-modifying antirheumatic drug; TCZ, tocilizumab.