# Cost-effectiveness of primary HPV genotyping and dual-stain or cytology reflex testing versus cytology-based screening for cervical cancer in Chile

**Authors:** Nicolas Armijo, Manuel A. Espinoza, Pilar Contreras-Montiel, Macarena Vera, Carlos Balmaceda

PMC · DOI: 10.1371/journal.pone.0332010 · PLOS One · 2026-03-04

## TL;DR

This study compares cervical cancer screening methods in Chile and finds that HPV DNA-based screening with dual-stain triage is more effective and cost-saving than traditional cytology.

## Contribution

The study evaluates HPV DNA-based screening strategies in Chile and identifies the most cost-effective approach for cervical cancer screening.

## Key findings

- HPV DNA-based screening with dual-stain triage (hrHPV–CINtec-5) provides the greatest health gain while remaining cost-saving.
- Transitioning from cytology to HPV DNA-based screening in Chile is projected to improve health outcomes and reduce costs.
- Probabilistic sensitivity analysis confirms the cost-effectiveness of HPV DNA-based strategies over traditional cytology.

## Abstract

Testing for high-risk human papillomavirus with genotyping for types 16 and 18 (HPV16/18) and triage by p16/Ki-67 dual-stain immunocytochemistry improves diagnostic performance in cervical cancer screening. We estimated the cost-effectiveness of HPV DNA–based primary screening strategies that detect high-risk genotypes every 5 years with either reflex cytology (hrHPV–Pap-5) or reflex dual stain (CINtec® PLUS, Roche; hereafter hrHPV–CINtec-5) versus cytology every 3 years (SoC (PAP-3)) among women aged 25–64 years, from the Chilean public healthcare perspective. A state-transition microsimulation reflected the natural history of cervical cancer in screening-eligible Chilean women, using local epidemiology and literature-informed inputs. Direct medical costs were obtained from official Chilean sources and converted to USD (1 USD = 938 CLP). Deterministic and probabilistic sensitivity analyses were conducted; a 30–64 years initiation scenario was also evaluated. Both high-risk HPV DNA-based strategies were more effective and cost-saving than SoC (PAP-3). In the 25–64 base case, hrHPV–CINtec-5 yielded the greatest health gain (13,003 incremental Quality-Adjusted Life Year, hereafter QALYs) with $16.65 saved per woman, while hrHPV–Pap-5 saved $32.57 with 12,844 QALYs. Probabilistic sensitivity analysis confirmed dominance (most simulations in the southeast quadrant) and cost-effectiveness acceptability >90% across willingness-to-pay ranges. Deterministic analysis highlighted progression risk from HPV16/18 and the discount rate as key drivers. Transitioning from PAP-3 to high-risk HPV DNA-based primary screening in Chile is projected to improve health outcomes while reducing costs. Among HPV DNA-based strategies detecting high-risk genotypes evaluated, triage with hrHPV–CINtec-5 provided the largest health gain while remaining cost-saving; hrHPV–Pap-5 maximized cost savings. These findings support modernizing the national screening program.

## Linked entities

- **Proteins:** CDKN2A (cyclin dependent kinase inhibitor 2A), Mki67 (antigen identified by monoclonal antibody Ki 67)
- **Diseases:** cervical cancer (MONDO:0002974)

## Full-text entities

- **Genes:** UBXN11 (UBX domain protein 11) [NCBI Gene 91544] {aka COA-1, PP2243, SOC, SOCI, UBXD5}, CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}, NPEPPS (aminopeptidase puromycin sensitive) [NCBI Gene 9520] {aka AAP-S, MP100, PSA}
- **Diseases:** Cancer (MESH:D009369), CIN 1-3 (MESH:D002578), anxiety (MESH:D001007), Cervical Cancer (MESH:D002583), HSIL (MESH:D000081483), CIN1-3 (MESH:C537153), cervical lesion (MESH:D002575), I (MESH:D006969), PLUS (OMIM:617303), infection (MESH:D007239), COVID-19 (MESH:D000086382), death (MESH:D003643), carcinogenic (MESH:D011230), FIGO stages II-IV (MESH:D062706), invasive disease (MESH:D009361), ASC-US (MESH:D065309), CINtec-5 (MESH:D008232)
- **Chemicals:** CINTec-5 (-), PAP (MESH:D010724)
- **Species:** Human papillomavirus (species) [taxon 10566], Pseudomonas sp. AP3 (species) [taxon 874293], Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus (species) [taxon 12721]

## Full text

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## Figures

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## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12959674/full.md

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Source: https://tomesphere.com/paper/PMC12959674