Extended Human Papillomavirus Genotyping to Predict Progression to High-Grade Cervical Precancer: A Prospective Cohort Study in the Southeastern United States

Author:

Bukowski Alexandra1ORCID,Hoyo Cathrine2ORCID,Hudgens Michael G.3ORCID,Brewster Wendy R.14ORCID,Valea Fidel5ORCID,Bentley Rex C.6ORCID,Vidal Adriana C.7ORCID,Maguire Rachel L.28ORCID,Schmitt John W.8ORCID,Murphy Susan K.8ORCID,North Kari E.1ORCID,Smith Jennifer S.19ORCID

Affiliation:

1. 1Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

2. 2Department of Biological Sciences, Center for Human Health and the Environment, North Carolina State University, Raleigh, North Carolina.

3. 3Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

4. 4Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

5. 5Department of Obstetrics and Gynecology, Virginia Tech Carilion School of Medicine, Roanoke, Virginia.

6. 6Department of Pathology, Duke University School of Medicine, Durham, North Carolina.

7. 7Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, California.

8. 8Department of Obstetrics and Gynecology, Duke University School of Medicine, Durham, North Carolina.

9. 9Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina.

Abstract

Abstract Background: High-risk human papillomavirus (hrHPV) testing is utilized in primary cervical cancer screening, generally along with cytology, to triage abnormalities to colposcopy. Most screening-based hrHPV testing involves pooled detection of any hrHPV or of HPV16/18. Cervical neoplasia progression risks based on extended hrHPV genotyping—particularly non-16/18 hrHPV types—are not well characterized. HPV genotype-specific incidence of high-grade cervical intraepithelial neoplasia or more severe (CIN2+) following an abnormal screening result was examined. Methods: We assessed a US-based prospective, multiracial, clinical cohort of 343 colposcopy patients with normal histology (n = 226) or CIN1 (n = 117). Baseline cervical samples underwent HPV DNA genotyping, and participants were followed up to 5 years. Genotype-specific CIN2+ incidence rates (IR) were estimated with accelerated failure time models. Five-year CIN2+ risks were estimated nonparametrically for hierarchical hrHPV risk groups (HPV16; else HPV18/45; else HPV31/33/35/52/58; else HPV39/51/56/59/68). Results: At enrollment, median participant age was 30.1 years; most (63%) were hrHPV-positive. Over follow-up, 24 participants progressed to CIN2+ (7.0%). CIN2+ IR among hrHPV-positive participants was 3.4/1,000 person-months. CIN2+ IRs were highest for HPV16 (8.3), HPV33 (7.8), and HPV58 (4.9). Five-year CIN2+ risk was higher for HPV16 (0.34) compared with HPV18/45 (0.12), HPV31/33/35/52/58 (0.12), and HPV39/51/56/59/68 (0.16) (P = 0.05). Conclusions: Non-16/18 hrHPV types are associated with differential CIN2+ progression rates. HPV16, 33, and 58 exhibited the highest rates over 5 years. HPV risk groups warrant further investigation in diverse US populations. Impact: These novel data assessing extended HPV genotyping in a diverse clinical cohort can inform future directions to improve screening practices in the general population.

Funder

NIH NCI

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology,Epidemiology

Reference36 articles.

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