Treatment of vulvar and vaginal dysplasia: plasma energy ablation versus carbon dioxide laser ablation.


Journal

International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
ISSN: 1525-1438
Titre abrégé: Int J Gynecol Cancer
Pays: England
ID NLM: 9111626

Informations de publication

Date de publication:
11 2021
Historique:
received: 30 06 2021
accepted: 14 09 2021
pubmed: 7 10 2021
medline: 27 1 2022
entrez: 6 10 2021
Statut: ppublish

Résumé

Plasma energy ablation vaporizes tissues similar to carbon dioxide laser ablation, but is not hindered by the unique hazards and regulation of laser technology. We aimed to evaluate the complication rate and effectiveness of plasma versus laser ablation in the treatment of vulvovaginal high-grade squamous intra-epithelial lesions (HSIL). We performed a retrospective cohort study of women treated with plasma or carbon dioxide laser ablation for histologically proven HSIL of the vulva or vagina from January 2014 to October 2019 at a single institution. Demographic factors, surgical characteristics, and complications were compared by ablation type using Fisher's exact tests. Recurrence-free survival was evaluated by ablation type using Kaplan-Meier curves, weighted log-rank tests, and Cox proportional hazards ratio estimates. Forty-two women were included; 50% underwent plasma and 50% underwent carbon dioxide laser ablation. Demographic factors were similar between the groups. 50% (n=21) were immunosuppressed, 45.2% (n=19) had prior vulvovaginal HSIL treatment, and 35.7% (n=15) were current smokers. Most women (n=25, 59.5%) were treated for vulvar HSIL, 38.1% (n=16) for vaginal HSIL. Complication rates did not differ by treatment: 9.5% (n=2) for laser ablation versus 4.8% (n=1) for plasma ablation (p Plasma energy ablation of vulvovaginal HSIL has similar complication rates and recurrence risk to carbon dioxide laser ablation. This technique could be considered as an alternative treatment modality for vulvovaginal HSIL and warrants further investigation.

Identifiants

pubmed: 34610972
pii: ijgc-2021-002913
doi: 10.1136/ijgc-2021-002913
pmc: PMC9415775
mid: NIHMS1743170
doi:

Types de publication

Comparative Study Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1410-1415

Subventions

Organisme : NCI NIH HHS
ID : P50 CA098252
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR003098
Pays : United States

Informations de copyright

© IGCS and ESGO 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: RS reports personal consulting fees from Astra Zeneca and is on an advisory board for GlaxoSmithKline, unrelated to the present work.

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Auteurs

Anna Beavis (A)

Department of Gynecology and Obstetrics, Johns Hopkins School of Medicine, Baltimore, Maryland, USA abeavis2@jhmi.edu.

Omar Najjar (O)

Department of Gynecology and Obstetrics, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

Tricia Murdock (T)

Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

Ashley Abing (A)

Department of Biology, Johns Hopkins University, Baltimore, Maryland, USA.

Amanda Fader (A)

Department of Gynecology and Obstetrics, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

Stephanie Wethington (S)

Department of Gynecology and Obstetrics, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

Rebecca Stone (R)

Department of Gynecology and Obstetrics, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

James Stuart Ferriss (JS)

Department of Gynecology and Obstetrics, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

Edward J Tanner (EJ)

Department of Obstetrics and Gynecology, Northwestern Medicine, Chicago, Illinois, USA.

Kimberly Levinson (K)

Department of Gynecology and Obstetrics, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

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