Optical coherence tomography versus punch biopsy for diagnosis of basal cell carcinoma: a multicentre, randomised, non-inferiority trial.


Journal

The Lancet. Oncology
ISSN: 1474-5488
Titre abrégé: Lancet Oncol
Pays: England
ID NLM: 100957246

Informations de publication

Date de publication:
08 2022
Historique:
received: 30 03 2022
revised: 01 06 2022
accepted: 09 06 2022
pubmed: 15 7 2022
medline: 2 8 2022
entrez: 14 7 2022
Statut: ppublish

Résumé

Punch biopsy is the gold standard for diagnosis and subtyping of basal cell carcinoma. The aim of this study was to assess whether use of optical coherence tomography (OCT), a non-invasive imaging tool, might avoid the need for biopsy. In a multicentre, randomised, non-inferiority trial, patients (aged ≥18 years) with an indication for biopsy of a suspected basal cell carcinoma outside the H-zone (high-risk zone) of the face were randomly assigned (1:1) to receive either OCT or punch biopsy (regular care) via a web-based randomisation system. Patients were enrolled from three participating centres in the Netherlands: Maastricht University Medical Centre+, Catharina Hospital Eindhoven, and Zuyderland Medical Centre Heerlen. Stratification factors for randomisation were participating centre and the grade of clinical basal cell carcinoma suspicion (high vs low). The primary endpoint was the proportion of patients free from a recurrent or residual lesion (malignant or premalignant) 12 months after treatment. Modified intention-to-treat and per-protocol analyses were conducted, with a predefined non-inferiority margin of -10%. This trial is registered with ClinicalTrials.gov number, NCT03848078, and is complete. Between Feb 25, 2019, and Sept 2, 2020, 598 patients were enrolled and randomly assigned to either the regular care group (n=299) or the OCT group (n=299). Data on the primary endpoint were available in 553 patients (n=268 in the regular care group, n=285 in the OCT group). After median follow-up of 12·7 months (IQR 11·2-14·1) in the OCT group and 12·6 months (10·8-14·3) in the regular care group, 253 (94%) of 268 patients in the OCT group and 266 (93%) of 285 patients in the regular care group were free from recurrent or residual lesions (malignant or pre-malignant) 12 months after treatment. According to our modified intention-to-treat analysis, the absolute difference (OCT vs regular care) was 1·07% (95% CI -2·93 to 5·06; one-sided p=0·30), with the lower limit of the 95% CI not exceeding the predefined non-inferiority margin of -10%. Per-protocol analyses led to proportions free from a residual or recurrent lesion (premalignant or malignant) of 95% (250 of 263) in the OCT group and 94% (262 of 278) in the regular care group, and an absolute difference of 0·81% (95% CI -2·98 to 4·60; one-sided p=0·34). OCT-guided diagnosis and treatment of basal cell carcinoma is non-inferior to regular care punch biopsy. Implementation of OCT for diagnosis of basal cell carcinoma could reduce the number of consultations and invasive procedures. The Netherlands Organization for Health Research and Development and Maurits en Anna de Kock Stichting.

Sections du résumé

BACKGROUND
Punch biopsy is the gold standard for diagnosis and subtyping of basal cell carcinoma. The aim of this study was to assess whether use of optical coherence tomography (OCT), a non-invasive imaging tool, might avoid the need for biopsy.
METHODS
In a multicentre, randomised, non-inferiority trial, patients (aged ≥18 years) with an indication for biopsy of a suspected basal cell carcinoma outside the H-zone (high-risk zone) of the face were randomly assigned (1:1) to receive either OCT or punch biopsy (regular care) via a web-based randomisation system. Patients were enrolled from three participating centres in the Netherlands: Maastricht University Medical Centre+, Catharina Hospital Eindhoven, and Zuyderland Medical Centre Heerlen. Stratification factors for randomisation were participating centre and the grade of clinical basal cell carcinoma suspicion (high vs low). The primary endpoint was the proportion of patients free from a recurrent or residual lesion (malignant or premalignant) 12 months after treatment. Modified intention-to-treat and per-protocol analyses were conducted, with a predefined non-inferiority margin of -10%. This trial is registered with ClinicalTrials.gov number, NCT03848078, and is complete.
FINDINGS
Between Feb 25, 2019, and Sept 2, 2020, 598 patients were enrolled and randomly assigned to either the regular care group (n=299) or the OCT group (n=299). Data on the primary endpoint were available in 553 patients (n=268 in the regular care group, n=285 in the OCT group). After median follow-up of 12·7 months (IQR 11·2-14·1) in the OCT group and 12·6 months (10·8-14·3) in the regular care group, 253 (94%) of 268 patients in the OCT group and 266 (93%) of 285 patients in the regular care group were free from recurrent or residual lesions (malignant or pre-malignant) 12 months after treatment. According to our modified intention-to-treat analysis, the absolute difference (OCT vs regular care) was 1·07% (95% CI -2·93 to 5·06; one-sided p=0·30), with the lower limit of the 95% CI not exceeding the predefined non-inferiority margin of -10%. Per-protocol analyses led to proportions free from a residual or recurrent lesion (premalignant or malignant) of 95% (250 of 263) in the OCT group and 94% (262 of 278) in the regular care group, and an absolute difference of 0·81% (95% CI -2·98 to 4·60; one-sided p=0·34).
INTERPRETATION
OCT-guided diagnosis and treatment of basal cell carcinoma is non-inferior to regular care punch biopsy. Implementation of OCT for diagnosis of basal cell carcinoma could reduce the number of consultations and invasive procedures.
FUNDING
The Netherlands Organization for Health Research and Development and Maurits en Anna de Kock Stichting.

Identifiants

pubmed: 35835136
pii: S1470-2045(22)00347-3
doi: 10.1016/S1470-2045(22)00347-3
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT03848078']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1087-1096

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests We declare no competing interests.

Auteurs

Fieke Adan (F)

Department of Dermatology, Maastricht University Medical Centre+, Maastricht, Netherlands; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, Netherlands. Electronic address: fieke.adan@mumc.nl.

Patty J Nelemans (PJ)

Department of Epidemiology, Maastricht University, Maastricht, Netherlands.

Brigitte A B Essers (BAB)

Department of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Centre+, Maastricht, Netherlands.

Tjinta Brinkhuizen (T)

Department of Dermatology, Maastricht University Medical Centre+, Maastricht, Netherlands; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, Netherlands; Department of Dermatology, Catharina Hospital, Eindhoven, Netherlands.

Sharon R P Dodemont (SRP)

Department of Dermatology, Catharina Hospital, Eindhoven, Netherlands.

Janneke P H M Kessels (JPHM)

Department of Dermatology, Zuyderland Medical Centre, Heerlen, Netherlands.

Patricia J F Quaedvlieg (PJF)

Department of Dermatology, Zuyderland Medical Centre, Heerlen, Netherlands.

Gert-Jan Dermont (GJ)

Department of Dermatology, Maastricht University Medical Centre+, Maastricht, Netherlands; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, Netherlands.

Veronique J L Winnepenninckx (VJL)

Department of Pathology, Maastricht University Medical Centre+, Maastricht, Netherlands.

Myrurgia Abdul Hamid (M)

Department of Pathology, Maastricht University Medical Centre+, Maastricht, Netherlands.

Nicole W J Kelleners-Smeets (NWJ)

Department of Dermatology, Maastricht University Medical Centre+, Maastricht, Netherlands; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, Netherlands.

Klara Mosterd (K)

Department of Dermatology, Maastricht University Medical Centre+, Maastricht, Netherlands; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, Netherlands.

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Classifications MeSH