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Revision of the Melanocytic Pathology Assessment Tool and Hierarchy for Diagnosis Classification Schema for Melanocytic Lesions: A Consensus Statement.
Barnhill, Raymond L; Elder, David E; Piepkorn, Michael W; Knezevich, Stevan R; Reisch, Lisa M; Eguchi, Megan M; Bastian, Boris C; Blokx, Willeke; Bosenberg, Marcus; Busam, Klaus J; Carr, Richard; Cochran, Alistair; Cook, Martin G; Duncan, Lyn M; Elenitsas, Rosalie; de la Fouchardière, Arnaud; Gerami, Pedram; Johansson, Iva; Ko, Jennifer; Landman, Gilles; Lazar, Alexander J; Lowe, Lori; Massi, Daniela; Messina, Jane; Mihic-Probst, Daniela; Parker, Douglas C; Schmidt, Birgitta; Shea, Christopher R; Scolyer, Richard A; Tetzlaff, Michael; Xu, Xiaowei; Yeh, Iwei; Zembowicz, Artur; Elmore, Joann G.
Afiliação
  • Barnhill RL; Department of Translational Research, Institut Curie, Unit of Formation and Research of Medicine University of Paris, Paris, France.
  • Elder DE; Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia.
  • Piepkorn MW; Division of Dermatology, Department of Medicine, University of Washington School of Medicine, Seattle.
  • Knezevich SR; Dermatopathology Northwest, Bellevue, Washington.
  • Reisch LM; Pathology Associates, Clovis, California.
  • Eguchi MM; Department of Biostatistics, University of Washington School of Medicine, Seattle.
  • Bastian BC; Department of Medicine, David Geffen School of Medicine at University of California, Los Angeles.
  • Blokx W; Departments of Pathology and Dermatology, University of California, San Francisco.
  • Bosenberg M; Department of Pathology, Division Laboratories, Pharmacy and Biomedical Genetics University Medical Center Utrecht, Utrecht, the Netherlands.
  • Busam KJ; Departments of Dermatology, Pathology, and Immunobiology, Yale School of Medicine, New Haven, Connecticut.
  • Carr R; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Cochran A; Cellular Pathology, South Warwickshire NHS Trust, Warwick, United Kingdom.
  • Cook MG; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at University of California, Los Angeles.
  • Duncan LM; Department of Histopathology, Royal Surrey NHS Foundation Trust, Guildford, United Kingdom.
  • Elenitsas R; Pathology Service, Massachusetts General Hospital, Harvard Medical School, Boston.
  • de la Fouchardière A; Department of Dermatology, Hospital of the University of Pennsylvania, Philadelphia.
  • Gerami P; Department of Biopathology, Centre Léon Bérard, Lyon, France.
  • Johansson I; University of Lyon, Université Claude Bernard Lyon 1, National Center for Scientific Research, Mixed Research Unit 5286, National Institute of Health and Medical Research U1052, Cancer Research Centre of Lyon, Lyon, France.
  • Ko J; Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Landman G; Department of Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Lazar AJ; Department of Anatomic Pathology, Cleveland Clinic, Cleveland, Ohio.
  • Lowe L; Department of Pathology, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Massi D; Departments of Pathology, Dermatology, and Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston.
  • Messina J; Departments of Pathology and Dermatology, University of Michigan, Ann Arbor.
  • Mihic-Probst D; Section of Pathology, Department of Health Sciences, University of Florence, Florence, Italy.
  • Parker DC; Departments of Pathology and Cutaneous Oncology, Moffitt Cancer Center, Tampa, Florida.
  • Schmidt B; Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
  • Shea CR; Departments of Pathology and Dermatology, Emory University School of Medicine, Atlanta, Georgia.
  • Scolyer RA; Department of Pathology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Tetzlaff M; Department of Dermatology, University of Chicago Medicine, Chicago, Illinois.
  • Xu X; Charles Perkins Centre, The University of Sydney, Sydney, Australia.
  • Yeh I; Melanoma Institute Australia, The University of Sydney, Sydney, Australia.
  • Zembowicz A; Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.
  • Elmore JG; Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital and NSW Health Pathology, Sydney, Australia.
JAMA Netw Open ; 6(1): e2250613, 2023 01 03.
Article em En | MEDLINE | ID: mdl-36630138
ABSTRACT
Importance A standardized pathology classification system for melanocytic lesions is needed to aid both pathologists and clinicians in cataloging currently existing diverse terminologies and in the diagnosis and treatment of patients. The Melanocytic Pathology Assessment Tool and Hierarchy for Diagnosis (MPATH-Dx) has been developed for this purpose.

Objective:

To revise the MPATH-Dx version 1.0 classification tool, using feedback from dermatopathologists participating in the National Institutes of Health-funded Reducing Errors in Melanocytic Interpretations (REMI) Study and from members of the International Melanoma Pathology Study Group (IMPSG). Evidence Review Practicing dermatopathologists recruited from 40 US states participated in the 2-year REMI study and provided feedback on the MPATH-Dx version 1.0 tool. Independently, member dermatopathologists participating in an IMPSG workshop dedicated to the MPATH-Dx schema provided additional input for refining the MPATH-Dx tool. A reference panel of 3 dermatopathologists, the original authors of the MPATH-Dx version 1.0 tool, integrated all feedback into an updated and refined MPATH-Dx version 2.0.

Findings:

The new MPATH-Dx version 2.0 schema simplifies the original 5-class hierarchy into 4 classes to improve diagnostic concordance and to provide more explicit guidance in the treatment of patients. This new version also has clearly defined histopathological criteria for classification of classes I and II lesions; has specific provisions for the most frequently encountered low-cumulative sun damage pathway of melanoma progression, as well as other, less common World Health Organization pathways to melanoma; provides guidance for classifying intermediate class II tumors vs melanoma; and recognizes a subset of pT1a melanomas with very low risk and possible eventual reclassification as neoplasms lacking criteria for melanoma. Conclusions and Relevance The implementation of the newly revised MPATH-Dx version 2.0 schema into clinical practice is anticipated to provide a robust tool and adjunct for standardized diagnostic reporting of melanocytic lesions and management of patients to the benefit of both health care practitioners and patients.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Melanoma Tipo de estudo: Diagnostic_studies / Guideline Limite: Humans Idioma: En Revista: JAMA Netw Open Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Melanoma Tipo de estudo: Diagnostic_studies / Guideline Limite: Humans Idioma: En Revista: JAMA Netw Open Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França