Reflectance confocal microscopy-guided carbon dioxide laser ablation of low-risk basal cell carcinomas: A prospective study.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 22 02 2019
revised: 13 04 2019
accepted: 08 06 2019
pubmed: 17 6 2019
medline: 15 2 2020
entrez: 17 6 2019
Statut: ppublish

Résumé

Basal cell carcinoma (BCC) treatment modalities can be stratified by tumor subtype and recurrence risk. The main limitation of nonsurgical treatment modalities is the lack of histopathologic confirmation. Reflectance confocal microscopy (RCM) is a noninvasive imaging device that provides quasihistologic images. To evaluate the feasibility and efficacy of RCM-guided carbon dioxide (CO Prospective study with biopsy specimen-proven low-risk BCCs imaged with RCM. RCM was performed on these sites before and after ablation. If residual tumor was found, a new series of laser passes were performed. The patients were then monitored for recurrence clinically and with RCM. Twenty-two tumor sites in 9 patients (5 men, 4 women) were imaged and treated. Median age was 59 ± 12.9 years (range, 30-74 years). Mean tumor size was 7.7 mm (range, 5-10 mm). Residual tumor was identified in 5 of 22 cases (22.7%) under RCM on immediate first-pass postablation sites, prompting additional laser passes. Median follow-up was 28.5 months (range, 22-32 months) with no recurrences found. Addition of RCM to laser ablation workflow can detect subclinical persistent tumor after initial ablation and may serve as an aid to increase the efficacy of laser ablation.

Sections du résumé

BACKGROUND BACKGROUND
Basal cell carcinoma (BCC) treatment modalities can be stratified by tumor subtype and recurrence risk. The main limitation of nonsurgical treatment modalities is the lack of histopathologic confirmation. Reflectance confocal microscopy (RCM) is a noninvasive imaging device that provides quasihistologic images.
OBJECTIVE OBJECTIVE
To evaluate the feasibility and efficacy of RCM-guided carbon dioxide (CO
METHODS METHODS
Prospective study with biopsy specimen-proven low-risk BCCs imaged with RCM. RCM was performed on these sites before and after ablation. If residual tumor was found, a new series of laser passes were performed. The patients were then monitored for recurrence clinically and with RCM.
RESULTS RESULTS
Twenty-two tumor sites in 9 patients (5 men, 4 women) were imaged and treated. Median age was 59 ± 12.9 years (range, 30-74 years). Mean tumor size was 7.7 mm (range, 5-10 mm). Residual tumor was identified in 5 of 22 cases (22.7%) under RCM on immediate first-pass postablation sites, prompting additional laser passes. Median follow-up was 28.5 months (range, 22-32 months) with no recurrences found.
CONCLUSIONS CONCLUSIONS
Addition of RCM to laser ablation workflow can detect subclinical persistent tumor after initial ablation and may serve as an aid to increase the efficacy of laser ablation.

Identifiants

pubmed: 31202871
pii: S0190-9622(19)30977-6
doi: 10.1016/j.jaad.2019.06.014
pmc: PMC6777957
mid: NIHMS1531870
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

984-988

Subventions

Organisme : NCI NIH HHS
ID : L30 CA231456
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

Copyright © 2019 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

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Auteurs

Cristian Navarrete-Dechent (C)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York; Department of Dermatology, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.

Miguel Cordova (M)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York.

Konstantinos Liopyris (K)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York.

Oriol Yélamos (O)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York; Dermatology Department, Hospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.

Saud Aleissa (S)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York.

Brian Hibler (B)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York; Department of Dermatology, Weill Cornell Medical College, New York, New York.

Heidy Sierra (H)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York; Department of Computer Science and Engineering, University of Puerto Rico Mayaguez, Mayaguez, Puerto Rico.

Aditi Sahu (A)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York.

Nina Blank (N)

Department of Dermatology, Weill Cornell Medical College, New York, New York.

Milind Rajadhyaksha (M)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York.

Anthony Rossi (A)

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York; Department of Dermatology, Weill Cornell Medical College, New York, New York. Electronic address: rossia@mskcc.org.

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Classifications MeSH