A Cross-Sectional Study of the Prevalence of Anal Dysplasia among Women with High-Grade Cervical, Vaginal, and Vulvar Dysplasia or Cancer: The PANDA Study.


Journal

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
ISSN: 1538-7755
Titre abrégé: Cancer Epidemiol Biomarkers Prev
Pays: United States
ID NLM: 9200608

Informations de publication

Date de publication:
05 12 2022
Historique:
received: 11 05 2022
revised: 25 07 2022
accepted: 16 09 2022
pubmed: 21 9 2022
medline: 7 12 2022
entrez: 20 9 2022
Statut: ppublish

Résumé

High-risk human papillomavirus (HR-HPV) infection is a risk factor for anal cancer, yet no anal cancer screening guidelines exist for women with lower genital tract HPV-related disease. We sought to describe the prevalence of anal HR-HPV or cytologic abnormalities in such women. This cross-sectional study was performed between October 2018 and December 2021. Inclusion criteria were ≥21 years of age and a prior diagnosis of high-grade dysplasia/cancer of the cervix, vagina, or vulva. Participants underwent anal cytology and anal/cervicovaginal HR-HPV testing. Women with abnormal anal cytology were referred for high-resolution anoscopy (HRA). 324 evaluable women were enrolled. Primary diagnosis was high-grade dysplasia/cancer of the cervix (77%), vagina (9%), and vulva (14%). Anal HR-HPV was detected in 92 patients (28%) and included HPV-16 in 24 (26%), HPV-18 in 6 (7%), and other HR-HPV types in 72 (78%) patients. Anal cytology was abnormal in 70 patients (23%) and included atypical squamous cells of undetermined significance (80%), low-grade squamous intraepithelial lesion (9%), high-grade intraepithelial lesion (HSIL; 1%), and atypical squamous cells-cannot rule out HSIL (10%). Of these patients, 55 (79%) underwent HRA. Anal biopsies were performed in 14 patients: 2 patients had anal intraepithelial neoplasia (AIN) 2/3, 1 patient had AIN 1, and 11 patients had negative biopsies. Both patients with AIN 2/3 had a history of cervical dysplasia. Our results suggest an elevated risk of anal HR-HPV infection and cytologic abnormalities in women with lower genital tract dysplasia/cancer. These results add to the growing body of evidence suggesting the need for evaluation of screening methods for anal dysplasia/cancer in this patient population to inform evidence-based screening recommendations.

Sections du résumé

BACKGROUND
High-risk human papillomavirus (HR-HPV) infection is a risk factor for anal cancer, yet no anal cancer screening guidelines exist for women with lower genital tract HPV-related disease. We sought to describe the prevalence of anal HR-HPV or cytologic abnormalities in such women.
METHODS
This cross-sectional study was performed between October 2018 and December 2021. Inclusion criteria were ≥21 years of age and a prior diagnosis of high-grade dysplasia/cancer of the cervix, vagina, or vulva. Participants underwent anal cytology and anal/cervicovaginal HR-HPV testing. Women with abnormal anal cytology were referred for high-resolution anoscopy (HRA).
RESULTS
324 evaluable women were enrolled. Primary diagnosis was high-grade dysplasia/cancer of the cervix (77%), vagina (9%), and vulva (14%). Anal HR-HPV was detected in 92 patients (28%) and included HPV-16 in 24 (26%), HPV-18 in 6 (7%), and other HR-HPV types in 72 (78%) patients. Anal cytology was abnormal in 70 patients (23%) and included atypical squamous cells of undetermined significance (80%), low-grade squamous intraepithelial lesion (9%), high-grade intraepithelial lesion (HSIL; 1%), and atypical squamous cells-cannot rule out HSIL (10%). Of these patients, 55 (79%) underwent HRA. Anal biopsies were performed in 14 patients: 2 patients had anal intraepithelial neoplasia (AIN) 2/3, 1 patient had AIN 1, and 11 patients had negative biopsies. Both patients with AIN 2/3 had a history of cervical dysplasia.
CONCLUSIONS
Our results suggest an elevated risk of anal HR-HPV infection and cytologic abnormalities in women with lower genital tract dysplasia/cancer.
IMPACT
These results add to the growing body of evidence suggesting the need for evaluation of screening methods for anal dysplasia/cancer in this patient population to inform evidence-based screening recommendations.

Identifiants

pubmed: 36126275
pii: 709291
doi: 10.1158/1055-9965.EPI-22-0548
pmc: PMC9729427
mid: NIHMS1838936
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2185-2191

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA101642
Pays : United States

Informations de copyright

©2022 American Association for Cancer Research.

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Auteurs

Samantha Batman (S)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Craig A Messick (CA)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Andrea Milbourne (A)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Ming Guo (M)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Mark F Munsell (MF)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Joel Fokom-Domgue (J)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Mila Salcedo (M)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Ashish Deshmukh (A)

The University of Texas Health Science Center, Houston, Texas.

Kristina R Dahlstrom (KR)

Baylor College of Medicine, Houston, Texas.

Mallory Ogburn (M)

The University of Texas Rio Grande Valley, Edinburg, Texas.

Anthony Price (A)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Nicole D Fleming (ND)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Jolyn Taylor (J)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Aaron Shafer (A)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Lauren Cobb (L)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Keith Sigel (K)

The Mount Sinai Hospital, New York, New York.

Erich M Sturgis (EM)

Baylor College of Medicine, Houston, Texas.

Elizabeth Y Chiao (EY)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Kathleen M Schmeler (KM)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

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Classifications MeSH