Assessment of a Diagnostic Classification System for Management of Lesions to Exclude Melanoma.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 12 2021
Historique:
entrez: 10 12 2021
pubmed: 11 12 2021
medline: 12 1 2022
Statut: epublish

Résumé

The proposed MOLEM (Management of Lesion to Exclude Melanoma) schema is more clinically relevant than Melanocytic Pathology Assessment Tool and Hierarchy for Diagnosis (MATH-Dx) for the management classification of melanocytic and nonmelanocytic lesions excised to exclude melanoma. A more standardized way of establishing diagnostic criteria will be crucial in the training of artificial intelligence (AI) algorithms. To examine pathologists' variability, reliability, and confidence in reporting melanocytic and nonmelanocytic lesions excised to exclude melanoma using the MOLEM schema in a population of higher-risk patients. This cohort study enrolled higher-risk patients referred to a primary care skin clinic in New South Wales, Australia, between April 2019 and December 2019. Baseline demographic characteristics including age, sex, and related clinical details (eg, history of melanoma) were collected. Patients with lesions suspicious for melanoma assessed by a primary care physician underwent clinical evaluation, dermoscopy imaging, and subsequent excision biopsy of the suspected lesion(s). A total of 217 lesions removed and prepared by conventional histologic method and stained with hematoxylin-eosin were reviewed by up to 9 independent pathologists for diagnosis using the MOLEM reporting schema. Pathologists evaluating for MOLEM schema were masked to the original histopathologic diagnosis. Characteristics of the lesions were described and the concordance of cases per MOLEM class was assessed. Interrater agreement and the agreement between pathologists' ratings and the majority MOLEM diagnosis were calculated by Gwet AC1 with quadratic weighting applied. The diagnostic confidence of pathologists was then assessed. A total of 197 patients were included in the study (102 [51.8%] male; 95 [48.2%] female); mean (SD) age was 64.2 (15.8) years (range, 24-93 years). Overall, 217 index lesions were assessed with a total of 1516 histological diagnoses. Of 1516 diagnoses, 677 (44.7%) were classified as MOLEM class I; 120 (7.9%) as MOLEM class II; 564 (37.2%) as MOLEM class III; 114 (7.5%) as MOLEM class IV; and 55 (3.6%) as MOLEM class V. Concordance rates per MOLEM class were 88.6% (class I), 50.8% (class II), 76.2% (class III), 77.2% (class IV), and 74.2% (class V). The quadratic weighted interrater agreement was 91.3%, with a Gwet AC1 coefficient of 0.76 (95% CI, 0.72-0.81). The quadratic weighted agreement between pathologists' ratings and majority MOLEM was 94.7%, with a Gwet AC1 coefficient of 0.86 (95% CI, 0.84-0.88). The confidence in diagnosis data showed a relatively high level of confidence (between 1.0 and 1.5) when diagnosing classes I (mean [SD], 1.3 [0.3]), IV (1.3 [0.3]) and V (1.1 [0.1]); while classes II (1.8 [0.2]) and III (1.5 [0.4]) were diagnosed with a lower level of pathologist confidence (≥1.5). The quadratic weighted interrater confidence rating agreement was 95.2%, with a Gwet AC1 coefficient of 0.92 (95% CI, 0.90-0.94) for the 1314 confidence ratings collected. The confidence agreement for each MOLEM class was 95.0% (class I), 93.5% (class II), 95.3% (class III), 96.5% (class IV), and 97.5% (class V). The proposed MOLEM schema better reflects clinical practice than the MPATH-Dx schema in lesions excised to exclude melanoma by combining diagnoses with similar prognostic outcomes for melanocytic and nonmelanocytic lesions into standardized classification categories. Pathologists' level of confidence appeared to follow the MOLEM schema diagnostic concordance trend, ie, atypical naevi and melanoma in situ diagnoses were the least agreed upon and the most challenging for pathologists to confidently diagnose.

Identifiants

pubmed: 34889949
pii: 2787002
doi: 10.1001/jamanetworkopen.2021.34614
pmc: PMC8665368
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2134614

Références

Australas J Dermatol. 2012 Nov;53(4):291-4
pubmed: 22497519
Br J Math Stat Psychol. 2008 May;61(Pt 1):29-48
pubmed: 18482474
J Am Acad Dermatol. 2012 Oct;67(4):727-35
pubmed: 22521204
JAMA Dermatol. 2013 Jun;149(6):699-709
pubmed: 23553375
JAMA Dermatol. 2018 Oct 1;154(10):1159-1166
pubmed: 30140929
Histopathology. 2008 Jan;52(2):139-46
pubmed: 18184263
Hum Pathol. 1996 Jun;27(6):528-31
pubmed: 8666360
J Am Acad Dermatol. 2014 Jan;70(1):131-41
pubmed: 24176521
J Med Imaging (Bellingham). 2020 Mar;7(2):027501
pubmed: 32341938
J Am Acad Dermatol. 2016 Aug;75(2):356-63
pubmed: 27189823
Dermatol Surg. 2006 May;32(5):738-44
pubmed: 16706773
J Am Acad Dermatol. 2018 Jul;79(1):52-59.e5
pubmed: 29524584
J Cutan Pathol. 2021 Jul;48(7):856-862
pubmed: 33433032
Nature. 2017 Feb 2;542(7639):115-118
pubmed: 28117445
J Am Acad Dermatol. 2010 May;62(5):751-6
pubmed: 20303612
BMJ. 2017 Jun 28;357:j2813
pubmed: 28659278
Lancet Oncol. 2001 Jul;2(7):443-9
pubmed: 11905739
J Clin Oncol. 1996 Apr;14(4):1218-23
pubmed: 8648377
N Engl J Med. 2019 Dec 12;381(24):2285-2287
pubmed: 31826337
JAMA. 2015 Mar 17;313(11):1122-32
pubmed: 25781441
BMJ Qual Saf. 2013 Oct;22 Suppl 2:ii21-ii27
pubmed: 23771902
Am J Clin Pathol. 2018 Aug 30;150(4):338-345
pubmed: 30007278
PLoS One. 2009;4(4):e5375
pubmed: 19404399
JAMA Intern Med. 2013 Nov 25;173(21):1952-8
pubmed: 23979070
Nat Commun. 2020 Aug 11;11(1):3923
pubmed: 32782264
Biometrics. 1977 Mar;33(1):159-74
pubmed: 843571

Auteurs

Ian Katz (I)

Southern Sun Pathology, Sydney, New South Wales, Australia.
University of Queensland, Brisbane, Queensland, Australia.

Blake O'Brien (B)

Sullivan Nicolaides Pathology, Brisbane, Queensland, Australia.

Simon Clark (S)

Douglass Hanly Moir Pathology, Sydney, New South Wales, Australia.

Curtis T Thompson (CT)

CTA Pathology, Portland, Oregon.

Brian Schapiro (B)

CTA Pathology, Portland, Oregon.

Anthony Azzi (A)

Newcastle Skin Check, Charlestown, New South Wales, Australia.

Alister Lilleyman (A)

Newcastle Skin Check, Charlestown, New South Wales, Australia.

Terry Boyle (T)

Allied Health and Human Performance, University of South Australia, Adelaide, South Australia, Australia.

Lore Jane L Espartero (LJL)

Future Industries Institute, University of South Australia, Adelaide, South Australia, Australia.

Miko Yamada (M)

Future Industries Institute, University of South Australia, Adelaide, South Australia, Australia.

Tarl W Prow (TW)

Future Industries Institute, University of South Australia, Adelaide, South Australia, Australia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH