Effect of Reflectance Confocal Microscopy for Suspect Lesions on Diagnostic Accuracy in Melanoma: A Randomized Clinical Trial.


Journal

JAMA dermatology
ISSN: 2168-6084
Titre abrégé: JAMA Dermatol
Pays: United States
ID NLM: 101589530

Informations de publication

Date de publication:
01 07 2022
Historique:
pubmed: 2 6 2022
medline: 23 7 2022
entrez: 1 6 2022
Statut: ppublish

Résumé

Previous systematic reviews and meta-analyses have concluded that given data paucity, a comparison of reflectance confocal microscopy (RCM) with dermoscopy is complex. They recommend comparative prospective studies in a real-world setting of suspect lesions. To test the hypothesis that RCM reduces unnecessary lesion excision by more than 30% and identifies all melanoma lesions thicker than 0.5 mm at baseline. This randomized clinical trial included 3165 patients enrolled from 3 dermatology referral centers in Italy between January 2017 and December 2019, with a mean (SD) follow-up of 9.6 (6.9) months (range, 1.9-37.0 months). The consecutive sample of 3165 suspect lesions determined through dermoscopy were eligible for inclusion (10 patients refused). Diagnostic analysis included 3078 patients (48 lost, 39 refused excision). Data were analyzed between April and September 2021. Patients were randomly assigned 1:1 to standard therapeutic care (clinical and dermoscopy evaluation) with or without adjunctive RCM. Information available guided prospective clinical decision-making (excision or follow-up). Hypotheses were defined prior to study initiation. All lesions excised (baseline and follow-up) were registered, including histopathological diagnoses/no change at dermoscopy follow-up (with or without adjunctive RCM). Number needed to excise (total number of excised lesions/number of melanomas) and Breslow thickness of delayed diagnosed melanomas were calculated based on real-life, prospective, clinical decision-making. Among the 3165 participants, 1608 (50.8%) were male, and mean (SD) age was 49.3 (14.9) years. When compared with standard therapeutic care only, adjunctive RCM was associated with a higher positive predictive value (18.9 vs 33.3), lower benign to malignant ratio (3.7:1.0 vs 1.8:1.0), and a number needed to excise reduction of 43.4% (5.3 vs 3.0). All lesions (n = 15) with delayed melanoma diagnoses were thinner than 0.5 mm. This randomized clinical trial shows that adjunctive use of RCM for suspect lesions reduces unnecessary excisions and assures the removal of aggressive melanomas at baseline in a real-life, clinical decision-making application for referral centers with RCM. ClinicalTrials.gov Identifier: NCT04789421.

Identifiants

pubmed: 35648432
pii: 2792714
doi: 10.1001/jamadermatol.2022.1570
pmc: PMC9161119
doi:

Banques de données

ClinicalTrials.gov
['NCT04789421']

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

754-761

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : ErratumIn

Auteurs

Giovanni Pellacani (G)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.
Dermatology Clinic, Sapienza University of Rome, Rome, Italy.

Francesca Farnetani (F)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.

Silvana Ciardo (S)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.

Johanna Chester (J)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.
Department of Surgery, Medicine, Dental Medicine and Morphological Sciences, University of Modena and Reggio Emilia, Modena, Italy.

Shaniko Kaleci (S)

Department of Surgery, Medicine, Dental Medicine and Morphological Sciences, University of Modena and Reggio Emilia, Modena, Italy.

Laura Mazzoni (L)

Skin Cancer Unit, Istituto Scientifico Romagnolo per lo Studio dei Tumori (IRST) IRCCS, Meldola, Italy.

Sara Bassoli (S)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.

Alice Casari (A)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.

Riccardo Pampena (R)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.
Skin Cancer Unit, Istituto Scientifico Romagnolo per lo Studio dei Tumori (IRST) IRCCS, Meldola, Italy.

Marica Mirra (M)

Centro Oncologico ad Alta Tecnologia Diagnostica, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Michela Lai (M)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.
Centro Oncologico ad Alta Tecnologia Diagnostica, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Serena Magi (S)

Skin Cancer Unit, Istituto Scientifico Romagnolo per lo Studio dei Tumori (IRST) IRCCS, Meldola, Italy.

Victor D Mandel (VD)

Skin Cancer Unit, Istituto Scientifico Romagnolo per lo Studio dei Tumori (IRST) IRCCS, Meldola, Italy.

Sergio Di Matteo (S)

Center of Research SAVE Study, Milan, Italy.

Giorgio Lorenzo Colombo (GL)

CEFAT Center of Pharmaceuticals Economics and Medical Technologies Evaluation, University of Pavia, Italy.

Ignazio Stanganelli (I)

Skin Cancer Unit, Istituto Scientifico Romagnolo per lo Studio dei Tumori (IRST) IRCCS, Meldola, Italy.
Dermatology Unit, University of Parma, Parma, Italy.

Caterina Longo (C)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.
Centro Oncologico ad Alta Tecnologia Diagnostica, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

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