Performance of Cervical Screening a Decade Following HPV Vaccination: The Costa Rica Vaccine Trial

Author:

Hu Shang-Ying12ORCID,Kreimer Aimée R2,Porras Carolina3,Guillén Diego3ORCID,Alfaro Mario3,Darragh Teresa M4,Stoler Mark H5,Villegas Luis F3,Ocampo Rebecca3,Rodriguez Ana Cecilia6,Schiffman Mark2,Tsang Sabrina H2,Lowy Douglas R27,Schiller John T7,Schussler John8,Quint Wim9,Gail Mitchell H2,Sampson Joshua N2ORCID,Hildesheim Allan2,Herrero Rolando310,

Affiliation:

1. Department of Cancer Epidemiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College , Beijing, China

2. Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health , Bethesda, MD, USA

3. Agencia Costarricense de Investigaciones Biomédicas (ACIB), Fundación INCIENSA , San José, Costa Rica

4. School of Medicine, University of California , San Francisco, CA, USA

5. Department of Pathology, University of Virginia , Charlottesville, VA, USA

6. Independent Consultant , San José, Costa Rica

7. Laboratory of Cellular Oncology, Center for Cancer Research, National Cancer Institute , Rockville, MD, USA

8. Information Management Services , Silver Spring, MD, USA

9. Viroclinics-DDL , Rijswijk, Netherlands

10. Early Detection Prevention and Infections, International Agency for Research on Cancer , Lyon, France

Abstract

Abstract Background We investigated the impact of human papillomavirus (HPV) vaccination on the performance of cytology-based and HPV-based screening for detection of cervical precancer among women vaccinated as young adults and reaching screening age. Methods A total of 4632 women aged 25-36 years from the Costa Rica HPV Vaccine Trial were included (2418 HPV-vaccinated as young adults and 2214 unvaccinated). We assessed the performance of cytology- and HPV-based cervical screening modalities in vaccinated and unvaccinated women to detect high-grade cervical precancers diagnosed over 4 years and the absolute risk of cumulative cervical precancers by screening results at entry. Results We detected 95 cervical intraepithelial neoplasia grade 3 or worse (52 in unvaccinated and 43 in vaccinated women). HPV16/18/31/33/45 was predominant (69%) among unvaccinated participants, and HPV35/52/58/39/51/56/59/66/68 predominated (65%) among vaccinated participants. Sensitivity and specificity of cervical screening approaches were comparable between women vaccinated as young adults and unvaccinated women. Colposcopy referral rates were lower in the vaccinated group for HPV-based screening modalities, but the positive predictive value was comparable between the 2 groups. Conclusions Among women approaching screening ages, vaccinated as young adults, and with a history of intensive screening, the expected reduction in the positive predictive value of HPV testing, associated with dropping prevalence of HPV-associated lesions, was not observed. This is likely due to the presence of high-grade lesions associated with nonvaccine HPV types, which may be less likely to progress to cancer.

Funder

The Costa Rica HPV Vaccine Trial

National Cancer Institute

NCI

National Institutes of Health Office of Research on Women’s Health

GlaxoSmithKline Biologicals

Clinical Trials Agreement

NCI with support from the National Institutes of Health Offices of Research on Women’s Health

Clinicaltrials.gov

Short Term Scientist Exchange Program (STSEP) at the NCI Center for Global Health

China Scholarship Council (CSC

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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