Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Jan 1;148(1):90-98.
doi: 10.1002/ijc.33198. Epub 2020 Jul 22.

Vulvar intraepithelial neoplasia: Incidence and long-term risk of vulvar squamous cell carcinoma

Affiliations

Vulvar intraepithelial neoplasia: Incidence and long-term risk of vulvar squamous cell carcinoma

Nikki B Thuijs et al. Int J Cancer. .

Abstract

The risk of vulvar squamous cell carcinoma (VSCC) in patients with high-grade vulvar intraepithelial neoplasia (VIN) is considered lower in high-grade squamous intraepithelial lesion (HSIL) compared to differentiated VIN (dVIN), but studies are limited. Our study investigated both the incidence of high-grade VIN and the cumulative incidence of VSCC in patients with HSIL and dVIN separately. A database of women diagnosed with high-grade VIN between 1991 and 2011 was constructed with data from the Dutch Pathology Registry (PALGA). The European standardized incidence rate (ESR) and VSCC risk were calculated, stratified for HSIL and dVIN. The effects of type of VIN (HSIL vs dVIN), age and lichen sclerosis (LS) were estimated by Cox regression. In total, 1148 patients were diagnosed with high-grade VIN between 1991 and 2011. Between 1991-1995 and 2006-2011, the ESR of HSIL increased from 2.39 (per 100 000 woman-years) to 3.26 and the ESR of dVIN increased from 0.02 to 0.08. The 10-year cumulative VSCC risk was 10.3%; 9.7% for HSIL and 50.0% for dVIN (log rank P < .001). Type of VIN, age and presence of LS were independent risk factors for progression to VSCC, with hazard ratios of 3.0 (95% confidence interval [CI] 1.3-7.1), 2.3 (95% CI 1.5-3.4) and 3.1 (95% CI 1.8-5.3), respectively. The incidence of high-grade VIN is rising. Because of the high cancer risk in patients with dVIN, better identification and timely recognition are urgently needed.

Keywords: HSIL; dVIN; incidence; vulvar intraepithelial neoplasia; vulvar squamous cell carcinoma.

PubMed Disclaimer

Conflict of interest statement

Renske Steenbergen is minority shareholder of Self‐screen B.V., a spin‐off company of VUmc. Self‐screen holds patents related to the detection of HPV‐induced cancers issued.

Nikki Thuijs, Marc van Beurden, Annette Bruggink, Hans Berkhof and Maaike Bleeker declare no conflicts of interest.

Figures

FIGURE 1
FIGURE 1
A, All high‐grade VIN. B, high‐grade VIN stratified for HSIL (blue line) and dVIN (red line). Interrupted lines represent VIN, both with and without concurrent VSCC. Continuous lines include VIN without concurrent VSCC. dVIN, differentiated VIN; HSIL, high‐grade squamous intraepithelial lesion; VIN, vulvar intraepithelial neoplasia; VSCC, vulvar squamous cell carcinoma [Color figure can be viewed at wileyonlinelibrary.com]
FIGURE 2
FIGURE 2
A, All high‐grade VIN. B, High‐grade VIN stratified for HSIL (blue line) and dVIN (red line). C, HSIL stratified for presence of LS (interrupted line) and absence of LS (continuous line). *after 14 years of follow‐up. dVIN, differentiated VIN; HSIL, high grade squamous intraepithelial lesion; LS, lichen sclerosus; VSCC, vulvar squamous cell carcinoma [Color figure can be viewed at wileyonlinelibrary.com]

References

    1. Pleunis N, Schuurman MS, Van Rossum MM, et al. Rare vulvar malignancies; incidence, treatment and survival in the Netherlands. Gynecol Oncol. 2016;142:440‐445. - PubMed
    1. Cohen PA, Anderson L, Eva L, Scurry J. Clinical and molecular classification of vulvar squamous pre‐cancers. Int J Gynecol Cancer. 2019;29:821‐828. - PubMed
    1. Hoang LN, Park KJ, Soslow RA, Murali R. Squamous precursor lesions of the vulva: current classification and diagnostic challenges. Pathology. 2016;48:291‐302. - PMC - PubMed
    1. de Sanjose S, Alemany L, Ordi J, et al. Worldwide human papillomavirus genotype attribution in over 2000 cases of intraepithelial and invasive lesions of the vulva. Eur J Cancer. 2013;49:3450‐3461. - PubMed
    1. Hinten F, Molijn A, Eckhardt L, et al. Vulvar cancer: two pathways with different localization and prognosis. Gynecol Oncol. 2018;149:310‐317. - PubMed

Publication types

MeSH terms