Journal article
Evaluation and Surgical Management of Pediatric Cutaneous Melanoma and Atypical Spitz and Non-Spitz Melanocytic Tumors (Melanocytomas): A Report From Children's Oncology Group
Journal of clinical oncology, Vol.43(9), pp.1157-1167
03/20/2025
DOI: 10.1200/JCO.24.01154
PMCID: PMC11908957
PMID: 39365959
Abstract
The purpose of this study was to develop recommendations for the diagnostic evaluation and surgical management of cutaneous melanoma (CM) and atypical Spitz tumors (AST) and non-Spitz melanocytic tumors (melanocytomas) in pediatric (age 0-10 years) and adolescent (age 11-18 years) patients.PURPOSEThe purpose of this study was to develop recommendations for the diagnostic evaluation and surgical management of cutaneous melanoma (CM) and atypical Spitz tumors (AST) and non-Spitz melanocytic tumors (melanocytomas) in pediatric (age 0-10 years) and adolescent (age 11-18 years) patients.A Children's Oncology Group-led panel with external, multidisciplinary CM specialists convened to develop recommendations on the basis of available data and expertise.METHODSA Children's Oncology Group-led panel with external, multidisciplinary CM specialists convened to develop recommendations on the basis of available data and expertise.Thirty-three experts from multiple specialties (cutaneous/medical/surgical oncology, dermatology, and dermatopathology) established recommendations with supporting data from 87 peer-reviewed publications.RESULTSThirty-three experts from multiple specialties (cutaneous/medical/surgical oncology, dermatology, and dermatopathology) established recommendations with supporting data from 87 peer-reviewed publications.(1) Excisional biopsies with 1-3 mm margins should be performed when feasible for clinically suspicious melanocytic neoplasms. (2) Definitive surgical treatment for CM, including wide local excision and sentinel lymph node biopsy (SLNB), should follow National Comprehensive Cancer Network Guidelines in the absence of data from pediatric-specific surgery trials and/or cohort studies. (3) Accurate classification of ASTs as benign or malignant is more likely with immunohistochemistry and next-generation sequencing. (4) It may not be possible to classify some ASTs as likely/definitively benign or malignant after clinicopathologic and/or molecular correlation, and these Spitz tumors of uncertain malignant potential should be excised with 5 mm margins. (5) ASTs favored to be benign should be excised with 1- to 3-mm margins if transected on biopsy. (6) Re-excision is not necessary if the AST does not extend to the biopsy margin(s) when complete/excisional biopsy was performed. (7) SLNB should not be performed for Spitz tumors unless a diagnosis of CM is favored on clinicopathologic evaluation. (8) Non-Spitz melanocytomas have a presumed increased risk for progression to CM and should be excised with 1- to 3-mm margins if transected on biopsy. (9) Re-excision of non-Spitz melanocytomas is not necessary if the lesion is completely excised on biopsy.RECOMMENDATIONS(1) Excisional biopsies with 1-3 mm margins should be performed when feasible for clinically suspicious melanocytic neoplasms. (2) Definitive surgical treatment for CM, including wide local excision and sentinel lymph node biopsy (SLNB), should follow National Comprehensive Cancer Network Guidelines in the absence of data from pediatric-specific surgery trials and/or cohort studies. (3) Accurate classification of ASTs as benign or malignant is more likely with immunohistochemistry and next-generation sequencing. (4) It may not be possible to classify some ASTs as likely/definitively benign or malignant after clinicopathologic and/or molecular correlation, and these Spitz tumors of uncertain malignant potential should be excised with 5 mm margins. (5) ASTs favored to be benign should be excised with 1- to 3-mm margins if transected on biopsy. (6) Re-excision is not necessary if the AST does not extend to the biopsy margin(s) when complete/excisional biopsy was performed. (7) SLNB should not be performed for Spitz tumors unless a diagnosis of CM is favored on clinicopathologic evaluation. (8) Non-Spitz melanocytomas have a presumed increased risk for progression to CM and should be excised with 1- to 3-mm margins if transected on biopsy. (9) Re-excision of non-Spitz melanocytomas is not necessary if the lesion is completely excised on biopsy.
Details
- Title: Subtitle
- Evaluation and Surgical Management of Pediatric Cutaneous Melanoma and Atypical Spitz and Non-Spitz Melanocytic Tumors (Melanocytomas): A Report From Children's Oncology Group
- Creators
- Michael R Sargen - National Institutes of HealthRaymond L Barnhill - Institut CurieDavid E Elder - Hospital of the University of PennsylvaniaSusan M Swetter - Stanford UniversityVictor G Prieto - The University of Texas MD Anderson Cancer CenterJennifer S Ko - Cleveland ClinicArmita Bahrami - Emory UniversityPedram Gerami - Northwestern UniversityArivarasan Karunamurthy - University of Pittsburgh Medical CenterAlberto S Pappo - St. Jude Children's Research HospitalLynn M Schuchter - University of PennsylvaniaPhilip E LeBoit - UCSF Helen Diller Family Comprehensive Cancer CenterIwei Yeh - UCSF Helen Diller Family Comprehensive Cancer CenterJohn M Kirkwood - University of Pittsburgh Medical CenterMelinda Jen - University of PennsylvaniaIra J Dunkel - Memorial Sloan Kettering Cancer CenterMegan M Durham - Children's Healthcare of AtlantaEmily R Christison-LagayMary T AustinJennifer H Aldrink - Nationwide Children's HospitalCasey Mehrhoff - Huntsman Cancer InstituteElena B Hawryluk - Massachusetts General HospitalEmily Y Chu - University of PennsylvaniaKlaus J Busam - Memorial Sloan Kettering Cancer CenterVernon Sondak - Moffitt Cancer CenterJane Messina - Moffitt Cancer CenterSusana Puig - Universitat de BarcelonaAndrew J Colebatch - Melanoma Institute AustraliaCarrie C Coughlin - Washington University in St. LouisKristen G Berrebi - University of IowaTheodore W Laetsch - Children's Hospital of PhiladelphiaSarah G Mitchell - Children's Healthcare of AtlantaBrittani Seynnaeve - University of Pittsburgh
- Resource Type
- Journal article
- Publication Details
- Journal of clinical oncology, Vol.43(9), pp.1157-1167
- DOI
- 10.1200/JCO.24.01154
- PMID
- 39365959
- PMCID
- PMC11908957
- NLM abbreviation
- J Clin Oncol
- ISSN
- 1527-7755
- eISSN
- 1527-7755
- Publisher
- LIPPINCOTT WILLIAMS & WILKINS
- Grant note
- Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI)National Institutes of Health (NIH)National Clinical Trials Network (NCTN)
The authors thank the Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), National Institutes of Health (NIH), and the National Clinical Trials Network (NCTN) for their support of this work.
- Language
- English
- Electronic publication date
- 10/04/2024
- Date published
- 03/20/2025
- Academic Unit
- Dermatology; Stead Family Department of Pediatrics
- Record Identifier
- 9984721241002771
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