A Systematic Review of Risk Factors for Development, Recurrence, and Progression of Vulvar Intraepithelial Neoplasia.


Journal

Journal of lower genital tract disease
ISSN: 1526-0976
Titre abrégé: J Low Genit Tract Dis
Pays: United States
ID NLM: 9704963

Informations de publication

Date de publication:
01 Apr 2022
Historique:
pubmed: 8 3 2022
medline: 25 3 2022
entrez: 7 3 2022
Statut: ppublish

Résumé

Vulvar intraepithelial neoplasia (VIN) is a premalignant condition with high recurrence rates despite treatment. Vulvar intraepithelial neoplasia develops through separate etiologic pathways relative to the presence or absence of human papillomavirus (HPV) and TP53 mutations. This systematic review was conducted (1) to identify historical risk factors for the development, recurrence, and progression of VIN and (2) to critique these risk factors in the context of advances made in the stratification of VIN based on HPV or TP53 status. A systematic search was performed on MEDLINE, Embase, Cochrane Database, PsychInfo, and CINAHL from inception to July 5, 2021. Three gynecologic oncologists independently evaluated the eligibility of studies based on predetermined inclusion and exclusion criteria, abstracted data, and then analyzed the relevant data. A total of 1,969 studies (involving 6,983 patients) were identified. Twenty-nine studies met inclusion criteria. The quality of evidence was low; primarily level 2b (Oxford Centre for Evidence-Based Medicine). Risk factors associated with the development of VIN include: smoking and coexisting vulvar dermatoses. Risk factors associated with recurrence include: smoking, multifocal disease, and positive surgical margins. Recent studies identified the presence of differentiated VIN/TP53 mutation as the most significant risk factor for both VIN recurrence and malignant progression. The current body of evidence consists primarily of small retrospective observational studies. Well-designed retrospective case-control series and/or prospective observational studies are urgently needed. Ideally, future studies will collect standardized data regarding associated risk factors and stratify women with VIN based on HPV and TP53 status.

Identifiants

pubmed: 35249976
doi: 10.1097/LGT.0000000000000662
pii: 00128360-202204000-00009
doi:

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

140-146

Informations de copyright

Copyright © 2022, ASCCP.

Déclaration de conflit d'intérêts

The authors have declared they have no conflicts of interest.

Références

Judson PL, Habermann EB, Baxter NN, et al. Trends in the incidence of invasive and in situ vulvar carcinoma. Obstet Gynecol 2006;107:1018–22.
Kang YJ, Smith M, Barlow E, et al. Vulvar cancer in high-income countries: increasing burden of disease. Int J Cancer 2017;141:2174–86.
Tessier-Cloutier B, Kortekaas KE, Thompson E, et al. Major p53 immunohistochemical patterns in in situ and invasive squamous cell carcinomas of the vulva and correlation with TP53 mutation status. Mod Pathol 2020;33:1595–605.
Singh N, Gilks CB. Vulval squamous cell carcinoma and its precursors. Histopathology 2020;76:128–38.
McAlpine JN, Kim SY, Akbari A, et al. HPV-independent differentiated vulvar intraepithelial neoplasia (dVIN) is associated with an aggressive clinical course. Int J Gynecol Cancer 2017;36:507–16.
Eva LJ, Ganesan R, Chan KK, et al. Differentiated-type vulval intraepithelial neoplasia has a high-risk association with vulval squamous cell carcinoma. Int J Gynecol Cancer 2009;19:741–4.
Thuijs NB, van Beurden M, Bruggink AH, et al. Vulvar intraepithelial neoplasia: incidence and long-term risk of vulvar squamous cell carcinoma. Int J Cancer 2021;148:90–8.
Satmary W, Holschneider CH, Brunette LL, et al. Vulvar intraepithelial neoplasia: risk factors for recurrence. Gynecol Oncol 2018;148:126–31.
Seters M. Vulvar Intraepithelial Neoplasia: New Concepts and Strategy [thesis] . Rotterdam, The Netherlands: Erasmus University; 2008.
Froeding L, Greimel E, Lanceley A, et al. Assessing patient-reported quality of life outcomes in vulva cancer patients: a systematic literature review. Int J Gynecol Cancer 2018;28:808–17.
Green MS, Naumann RW, Elliot M, et al. Sexual dysfunction following vulvectomy. Gynecol Oncol 2000;77:73–7.
Aerts L, Enzlin P, Vergote I, et al. Sexual, psychological, and relational functioning in women after surgical treatment for vulvar malignancy: a literature review. J Sex Med 2019;9:361–71.
Andreasson B, Bock JE. Intraepithelial neoplasia in the vulvar region. Gynecol Oncol 1985;21:300–5.
Barbero M, Micheletti L, Preti M, et al. Biologic behavior of vulvar intraepithelial neoplasia. Histologic and clinical parameters. J Reprod Med 1993;38:108–12.
Hording U, Junge J, Poulsen H, et al. Vulvar intraepithelial neoplasia III: a viral disease of undetermined progressive potential. Gynecol Oncol 1995;56:276–9.
Korn AP, Abercrombie PD, Foster A. Vulvar intraepithelial neoplasia in women infected with human immunodeficiency virus-1. Gynecol Oncol 1996;61:384–6.
Herod JJ, Shafi MI, Rollason TP, et al. Vulvar intraepithelial neoplasia: long term follow up of treated and untreated women. Br J Obstet Gynaecol 1996;103:446–52.
Junge J, Poulsen H, Horn T, et al. Prognosis of vulvar dysplasia and carcinoma in situ with special reference to histology and types of human papillomavirus (HPV). APMIS 1997;105:963–71.
Kuppers V, Stiller M, Somville T, et al. Risk factors for recurrent VIN. Role of multifocality and grade of disease. J Reprod Med 1997;42:140–4.
Modesitt SC, Waters AB, Walton L, et al. Vulvar intraepithelial neoplasia III: occult cancer and the impact of margin status on recurrence. Obstet Gynecol 1998;92:962–6.
Basta A, Adamek K, Pitynski K. Intraepithelial neoplasia and early stage vulvar cancer. Epidemiological, clinical and virological observations. Eur J Gynaecol Oncol 1999;20:111–4.
Sykes P, Smith N, McCormick P, et al. High-grade vulval intraepithelial neoplasia (VIN 3): a retrospective analysis of patient characteristics, management, outcome and relationship to squamous cell carcinoma of the vulva 1989–1999. Aust N Z J Obstet Gynaecol 2002;42:69–74.
Chulvis do Val IC, Almeida Filho GL, Valiante PM, et al. Vulvar intraepithelial neoplasia p53 expression, p53 gene mutation and HPV in recurrent/progressive cases. J Reprod Med 2004;49:868–74.
Jones R, Rowan DM, Stewart AW. Vulvar intraepithelial neoplasia: aspects of the natural history and outcome in 405 women. Obstet Gynecol Surv 2006;61:176–7.
Hillemanns P, Wang X, Staehle S, et al. Evaluation of different treatment modalities for vulvar intraepithelial neoplasia (VIN): CO(2) laser vaporization, photodynamic therapy, excision and vulvectomy. Gynecol Oncol 2006;100:271–5.
van de Nieuwenhof HP, Massuger LF, van der Avoort IA, et al. Vulvar squamous cell carcinoma development after diagnosis of VIN increases with age. Eur J Cancer 2009;45:851–6.
Frega A, Sopracordevole F, Scirpa P, et al. The re-infection rate of high-risk HPV and the recurrence rate of vulvar intraepithelial neoplasia (VIN) usual type after surgical treatment. Med Sci Monit 2011;17:CR532–5.
Nugent EK, Brooks RA, Barr CD, et al. Clinical and pathologic features of vulvar intraepithelial neoplasia in premenopausal and postmenopausal women. J Low Genit Tract Dis 2011;15:15–9.
Wallbillich JJ, Rhodes HE, Milbourne AM, et al. Vulvar intraepithelial neoplasia (VIN 2/3): comparing clinical outcomes and evaluating risk factors for recurrence. Gynecol Oncol 2012;127:312–5.
Frega A, Sesti F, Sopracordevole F, et al. Imiquimod 5% cream versus cold knife excision for treatment of VIN 2/3: a five-year follow-up. Eur Rev Med Pharmacol Sci 2013;17:936–40.
Fehr MK, Baumann M, Mueller M, et al. Disease progression and recurrence in women treated for vulvovaginal intraepithelial neoplasia. J Gynecol Oncol 2013;24:236–41.
van Esch EM, Dam MC, Osse ME, et al. Clinical characteristics associated with development of recurrence and progression in usual-type vulvar intraepithelial neoplasia. Int J Gynecol Cancer 2013;23:1476–83.
Gentile M, Bianchi P, Sesti F, et al. Adjuvant topical treatment with imiquimod 5% after excisional surgery for VIN 2/3. Eur Rev Med Pharmacol Sci 2014;18:2949–52.
Bradbury M, Cabrera S, Garcia-Jimenez A, et al. Vulvar intraepithelial neoplasia: clinical presentation, management and outcomes in women infected with HIV. AIDS 2016;30:859–68.
Brinton LA, Thistle JE, Liao LM, et al. Epidemiology of vulvar neoplasia in the NIH-AARP study. Gynecol Oncol 2017;145:298–304.
Bogani G, Martinelli F, Ditto A, et al. The association of pre-treatment HPV subtypes with recurrence of VIN. Eur J Obstet Gynecol Reprod Biol 2017;211:37–41.
Ayakannu T, Murugesu S, Taylor AH, et al. The impact of focality and centricity on vulvar intraepithelial neoplasia on disease progression in HIV+ patients: a 10-year retrospective study. Dermatology 2019;235:327–33.
Howick J, Chalmers I, Glasziou P, et al. The Oxford levels of evidence 2. [Internet]. 2011. Available at: https://www.cebm.ox.ac.uk/resources/levels-of-evidence/ocebm-levels-of-evidence . Accessed September 15, 2021.
van Seters M, van Beurden M, de Craen AJ. Is the assumed natural history of vulvar intraepithelial neoplasia III based on enough evidence? A systematic review of 3322 published patients. Gynecol Oncol 2005;97:645–51.
Moch H. Female Genital Tumours: WHO Classification of Tumours . 5th Edition, Volume 4. Lyon, France: International Agency for Research on Cancer; 2020.
Perkins RB, Guido RS, Castle PE, et al. 2019 ASCCP Risk-Based Management Consensus Guidelines for abnormal cervical cancer screening tests and cancer precursors. J Low Genit Tract Dis 2020;24:102–31.
Cheng AS, Karnezis AN, Jordan S, et al. p16 Immunostaining allows for accurate subclassification of vulvar squamous cell carcinoma into HPV-associated and HPV-independent cases. Int J Gynecol Pathol 2016;35:385–93.

Auteurs

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH