Table A1.
a) Inputs | Reported? (Y/N) | Reported by age? (Y/N) | Report by sex? | Comments |
---|---|---|---|---|
Vaccine uptake | Y | Y | Y | Uptake by number of doses, age, sex |
Vaccine efficacy | Y | Y | Y | Efficacy by number of doses, age, sex, HPV type |
Vaccine cross-protection | Y | N/A | N/A | Level and duration of protection by dose and type. |
Duration vaccine protection and waning | Y | Y | Y (report by sex and site/disease if applicable) | Duration of vaccine protection and waning assumptions. Report base case assumption and sensitivity analysis on duration of protection |
Vaccine and delivery costs | Y | Y (if applicable) | Y (if applicable) | Vaccine-related cost assumptions (by sex if they differ) including infrastructure (overhead), administration, cost per dose. Delivery mechanism |
Pre-vaccination disease burden (including population attributable fractions for HPV) | Y | Y | Y (if applicable) | Pre-vaccination disease burden included when assessing effect on infections and cancer or pre-vaccination cancer burden for population attributable fractions. |
Duration of natural immunity |
Y |
Y |
Y |
Comment on waning function |
b) Outputs |
Reported? (Y/N) |
Report by age? (Y/N) |
Report by sex? (B, F, or M) |
Report as calibration or validation target? (Y/N) |
Absolute reductions in HPV infections, and/or warts, post-vaccination | Y | Y | As appropriate to evaluation | Y |
Absolute reductions in CIN2+ post-vaccination | Y | Y | As appropriate to evaluation | Y. Suggested comparison to vaccine trial data; consideration should be given to trial-based modelling to support this validation process, and/or comment should be made on the applicability and external validity of the trial data to the situation being modelled. |
Absolute reductions in invasive cancer (cervical and other HPV cancers, as relevant) post-vaccination | Y | Y | As appropriate to evaluation | Y |
B: both sexes; CIN2+: cervical intraepithelial neoplasia grade 2 and above; F: female; male; N: no; Y: yes.