Melanoma recognition by a deep learning convolutional neural network-Performance in different melanoma subtypes and localisations.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
03 2020
Historique:
received: 22 08 2019
revised: 21 10 2019
accepted: 16 11 2019
pubmed: 24 1 2020
medline: 1 8 2020
entrez: 24 1 2020
Statut: ppublish

Résumé

Deep learning convolutional neural networks (CNNs) show great potential for melanoma diagnosis. Melanoma thickness at diagnosis among others depends on melanoma localisation and subtype (e.g. advanced thickness in acrolentiginous or nodular melanomas). The question whether CNN may counterbalance physicians' diagnostic difficulties in these melanomas has not been addressed. We aimed to investigate the diagnostic performance of a CNN with approval for the European market across different melanoma localisations and subtypes. The current market version of a CNN (Moleanalyzer-Pro®, FotoFinder Systems GmbH, Bad Birnbach, Germany) was used for classifications (malignant/benign) in six dermoscopic image sets. Each set included 30 melanomas and 100 benign lesions of related localisations and morphology (set-SSM: superficial spreading melanomas and macular nevi; set-LMM: lentigo maligna melanomas and facial solar lentigines/seborrhoeic keratoses/nevi; set-NM: nodular melanomas and papillomatous/dermal/blue nevi; set-Mucosa: mucosal melanomas and mucosal melanoses/macules/nevi; set-AM The CNN showed a high-level performance in set-SSM, set-NM and set-LMM (sensitivities >93.3%, specificities >65%, receiver operating characteristics-area under the curve [ROC-AUC] >0.926). In set-AM The CNN may help to partly counterbalance reduced human accuracies. However, physicians need to be aware of the CNN's limited diagnostic performance in mucosal and subungual lesions. Improvements may be expected from additional training images of mucosal and subungual sites.

Sections du résumé

BACKGROUND
Deep learning convolutional neural networks (CNNs) show great potential for melanoma diagnosis. Melanoma thickness at diagnosis among others depends on melanoma localisation and subtype (e.g. advanced thickness in acrolentiginous or nodular melanomas). The question whether CNN may counterbalance physicians' diagnostic difficulties in these melanomas has not been addressed. We aimed to investigate the diagnostic performance of a CNN with approval for the European market across different melanoma localisations and subtypes.
METHODS
The current market version of a CNN (Moleanalyzer-Pro®, FotoFinder Systems GmbH, Bad Birnbach, Germany) was used for classifications (malignant/benign) in six dermoscopic image sets. Each set included 30 melanomas and 100 benign lesions of related localisations and morphology (set-SSM: superficial spreading melanomas and macular nevi; set-LMM: lentigo maligna melanomas and facial solar lentigines/seborrhoeic keratoses/nevi; set-NM: nodular melanomas and papillomatous/dermal/blue nevi; set-Mucosa: mucosal melanomas and mucosal melanoses/macules/nevi; set-AM
RESULTS
The CNN showed a high-level performance in set-SSM, set-NM and set-LMM (sensitivities >93.3%, specificities >65%, receiver operating characteristics-area under the curve [ROC-AUC] >0.926). In set-AM
CONCLUSIONS
The CNN may help to partly counterbalance reduced human accuracies. However, physicians need to be aware of the CNN's limited diagnostic performance in mucosal and subungual lesions. Improvements may be expected from additional training images of mucosal and subungual sites.

Identifiants

pubmed: 31972395
pii: S0959-8049(19)30864-0
doi: 10.1016/j.ejca.2019.11.020
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

21-29

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement FotoFinder Systems GmbH had no role in the study design or interpretation of the data. T Fuchs is an employed software developer at the research and development department of FotoFinder Systems GmbH and was responsible for technical support and for writing parts of the supplement method section covering details on the CNN architecture and training. HA Haenssle received honoraria and/or travel expenses from companies involved in the development of devices for skin cancer screening: Scibase AB, FotoFinder Systems GmbH, Heine Optotechnik GmbH, Magnosco GmbH. A Blum received honoraria and/or travel expenses from companies involved in the development of devices for skin cancer screening: Scibase AB, FotoFinder Systems GmbH, Heine Optotechnik GmbH. All other authors indicated no conflict of interest.

Auteurs

Julia K Winkler (JK)

Department of Dermatology, University of Heidelberg, Heidelberg, Germany.

Katharina Sies (K)

Department of Dermatology, University of Heidelberg, Heidelberg, Germany.

Christine Fink (C)

Department of Dermatology, University of Heidelberg, Heidelberg, Germany.

Ferdinand Toberer (F)

Department of Dermatology, University of Heidelberg, Heidelberg, Germany.

Alexander Enk (A)

Department of Dermatology, University of Heidelberg, Heidelberg, Germany.

Teresa Deinlein (T)

Department of Dermatology and Venerology, Medical University of Graz, Graz, Austria.

Rainer Hofmann-Wellenhof (R)

Department of Dermatology and Venerology, Medical University of Graz, Graz, Austria.

Luc Thomas (L)

Hospices Civils de Lyon, Department of Dermatology, Lyon Sud University Hospital, Pierre Bénite, France.

Aimilios Lallas (A)

First Department of Dermatology, Aristotle University, Thessaloniki, Greece.

Andreas Blum (A)

Public, Private and Teaching Practice, Konstanz, Germany.

Wilhelm Stolz (W)

Department of Dermatology, Allergology and Environmental Medicine II, Hospital Thalkirchner Street, Munich, Germany.

Mohamed S Abassi (MS)

Faculty of Computer Science and Mathematics, University of Passau, Passau, Germany.

Tobias Fuchs (T)

Department of Research and Development, FotoFinder Systems GmbH, Bad Birnbach, Germany.

Albert Rosenberger (A)

Institute of Genetic Epidemiology at the Center of Statistics, University of Goettingen, Goettingen, Germany.

Holger A Haenssle (HA)

Department of Dermatology, University of Heidelberg, Heidelberg, Germany. Electronic address: holger.haenssle@med.uni-heidelberg.de.

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