Pre-Vaccination Human Papillomavirus Genotypes and HPV16 Variants among Women Aged 25 Years or Less with Cervical Cancer

Author:

Jayasinghe Yasmin L.123ORCID,Tabrizi Sepehr N.14,Stevens Matthew5,Leong Trishe Y-M.6,Pyman Jan7,Grover Sonia R.238,Garland Suzanne M.134,

Affiliation:

1. Department of Obstetrics and Gynaecology, Royal Women’s Hospital, The University of Melbourne, Melbourne, VIC 3010, Australia

2. Department of Gynaecology, Royal Children’s Hospital, Melbourne, VIC 3010, Australia

3. Murdoch Children’s Research Institute, Melbourne, VIC 3052, Australia

4. Women’s Centre for Infectious Diseases, Royal Women’s Hospital, Melbourne, VIC 3010, Australia

5. The Australian Genome Research Facility, Melbourne, VIC 3050, Australia

6. Department of Anatomical Pathology, St. Vincents Hospital, Melbourne, VIC 3000, Australia

7. Department of Anatomical Pathology, Royal Women’s Hospital, Melbourne, VIC 3010, Australia

8. Department of Paediatrics, University of Melbourne, Melbourne, VIC 3052, Australia

Abstract

Background: In 2007, Australia introduced a national human papillomavirus (HPV) vaccination program. In 2017, the onset of cervical screening changed from 18 to 25 years of age, utilising human papillomavirus (HPV) nucleic acid testing. The objective of the study is to describe the HPV genotypes and HPV16 variants in biopsies from women ≤ 25 years of age with cervical carcinoma (CC) (cases), compared with those aged >25 years (controls), in a pre-vaccination cohort. Methods: HPV genotyping of archival paraffin blocks (n = 96) was performed using the INNO-LiPA HPV Genotyping assay. HPV16-positive samples were analysed for variants by type-specific PCR spanning L1, E2 and E6 regions. Results: HPV16 was the commonest genotype in cases (54.5%, 12/22) and controls (66.7%, 46/69) (p = 0.30), followed by HPV18 (36.3%, 8/22 vs. 17.3% 12/69, respectively) (p = 0.08). Furthermore, 90% (20/22) of cases and 84.1% (58/69) of controls were positive for HPV16 or 18 (p = 0.42); 100% (22/22) of cases and 95.7% (66/69) of controls had at least one genotype targeted by the nonavalent vaccine (p = 0.3). The majority of HPV16 variants (87.3%, 48/55) were of European lineage. The proportion of unique nucleotide substitutions was significantly higher in cases (83.3%, 10/12) compared with controls (34.1%, 15/44), (p < 0.003, χ2, OR 9.7, 95%CI 1.7–97.7). Conclusions: Virological factors may account for the differences in CCs observed in younger compared with older women. All CCs in young women in this study had preventable 9vHPV types, which is important messaging for health provider adherence to new cervical screening guidelines.

Funder

Victorian Cancer Agency

National Health and Medical Research Council

Royal Australian and New Zealand College of Obstetricians and Gynaecologists Research Foundation

Cancer Council of Victoria

Royal Australasian College of Physicians

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

Reference37 articles.

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2. Clinicians’ attitude towards changes in Australian National Cervical Screening Program;Yap;J. Clin. Virol.,2016

3. Primary HPV DNA based cervical cancer screening at 25 years: Views of young Australian women aged 16–28 years;Jayasinghe;J. Clin. Virol.,2016

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5. Australian National Cervical Screening Program renewal: Attitudes and experiences of general practitioners, and obstetricians and gynaecologists;Obermair;Aust. N. Z. J. Obstet. Gynaecol.,2021

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