Table 4

Sensitivity analyses restricted to 2006–2012, on first tumour necrosis factor inhibitor (TNFi) (‘on drug’) and continuous time on TNFi treatment (“on class’), respectively

AnalysisOutcomeCohort comparisonn eventsPerson-yearsHR*
2006–2012 and stricter definition of biologics-naive RA†CIN 1TNFi4041 9381.02 (0.67 to 1.54)
New TNFi users‡2116 7251.12 (0.67 to 1.87)
Biologics-naive RA5988 696Ref
General population6371 394 5190.59 (0.45 to 0.78)
CIN 2+TNFi5842 4291.10 (0.72 to 1.68)
New TNFi users‡3016 9161.09 (0.72 to 1.66)
Biologics-naive RA8989 385Ref
General population10031 403 8020.59 (0.47 to 0.73)
Invasive cervical cancerTNFi1045 5571.36 (0.59 to 3.13)
New TNFi users‡118 110§
Biologics-naive RA1794 590Ref
General population2071 474 6950.73 (0.44 to 1.21)
On drugCIN 1TNFi3029 0941.23 (0.81 to 1.88)
Biologics-naive RA99173 369Ref
CIN 2+TNFi5029 4071.60 (1.15 to 2.22)
Biologics-naive RA137174 514Ref
Invasive cervical cancerTNFi531 4991.46 (0.54 to 3.94)
Biologics-naive RA25184 391Ref
On classCIN 1TNFi3736 6991.21 (0.82 to 1.78)
Biologics-naive RA99173 369Ref
CIN 2+TNFi5937 1001.50 (1.09 to 2.05)
Biologics-naive RA137174 514Ref
Invasive cervical cancerTNFi839 8451.81 (0.78 to 4.18)
Biologics-naive RA25184 391Ref
  • HRs (HRs model a–c) and 95% CIs comparing each outcome between cohorts.

  • *Stratified on decade of birth and adjusted for educational level, number of cervical screens past five years, comorbidities, marital status and total days spent in hospital during last five years, also implicitly adjusted for age since age was used as the model's timescale.

  • †The biologics-naive RA cohort was restricted to patients who initiated or were on treatment with at least two of any of the commonly used non-biological DMARDs (methotrexate, sulfasalazine, antimalarials or leflunomide).

  • ‡TNFi cohort restricted to patients who started their first TNFi treatment 2006 or later.

  • §Not computed due to low number of events.

  • CIN, cervical intraepithelial neoplasia; DMARD, disease-modifying antirheumatic drug; RA, rheumatoid arthritis.