| Title: | Estimated Prevalence, Tumor Spectrum, and Neurofibromatosis Type 1-Like Phenotype of CDKN2A-Related Melanoma-Astrocytoma Syndrome |
| Journal: | JAMA Dermatology |
| Published: | 1 Oct 2023 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/37585199/ |
| DOI: | https://doi.org/10.1001/jamadermatol.2023.2621 |
| URL: | https://jamanetwork.com/journals/jamadermatology/articlepdf/2808644/jamadermatology_sargen_2023_br_230012_1697555574.19053.pdf |
| Citations: | 4 (4 in last 2 years) as of 8 Aug 2024 |
Publication 9438
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Abstract
Importance: Knowledge about the prevalence and tumor types of CDKN2A-related melanoma-astrocytoma syndrome (MAS) is limited and could improve disease recognition.</p>
Objective: To estimate the prevalence and describe the tumor types of MAS.</p>
Design, Setting, and Participants: This retrospective cohort study analyzed all available MAS cases from medical centers in the US (2 sites) and Europe (2 sites) and from biomedical population genomic databases (UK Biobank [United Kingdom], Geisinger MyCode [US]) between January 1, 1976, and December 31, 2020. Patients with MAS with CDKN2A germline pathogenic variants and 1 or more neural tumors were included. Data were analyzed from June 1, 2022, to January 31, 2023.</p>
Main Outcomes and Measures: Disease prevalence and tumor frequency.</p>
Results: Prevalence of MAS ranged from 1 in 170 503 (n = 1 case; 95% CI, 1:30 098-1:965 887) in Geisinger MyCode (n = 170 503; mean [SD] age, 58.9 [19.1] years; 60.6% women; 96.2% White) to 1 in 39 149 (n = 12 cases; 95% CI, 1:22 396-1:68 434) in UK Biobank (n = 469 789; mean [SD] age, 70.0 [8.0] years; 54.2% women; 94.8% White). Among UK Biobank patients with MAS (n = 12) identified using an unbiased genomic ascertainment approach, brain neoplasms (4 of 12, 33%; 1 glioblastoma, 1 gliosarcoma, 1 astrocytoma, 1 unspecified type) and schwannomas (3 of 12, 25%) were the most common malignant and benign neural tumors, while cutaneous melanoma (2 of 12, 17%) and head and neck squamous cell carcinoma (2 of 12, 17%) were the most common nonneural malignant neoplasms. In a separate case series of 14 patients with MAS from the US and Europe, brain neoplasms (4 of 14, 29%; 2 glioblastomas, 2 unspecified type) and malignant peripheral nerve sheath tumor (2 of 14, 14%) were the most common neural cancers, while cutaneous melanoma (4 of 14, 29%) and sarcomas (2 of 14, 14%; 1 liposarcoma, 1 unspecified type) were the most common nonneural cancers. Cutaneous neurofibromas (7 of 14, 50%) and schwannomas (2 of 14, 14%) were also common. In 1 US family, a father and son with MAS had clinical diagnoses of neurofibromatosis type 1 (NF1). Genetic testing of the son detected a pathogenic CDKN2A splicing variant (c.151-1G>C) and was negative for NF1 genetic alterations. In UK Biobank, 2 in 150 (1.3%) individuals with clinical NF1 diagnoses had likely pathogenic variants in CDKN2A, including 1 individual with no detected variants in the NF1 gene.</p>
Conclusions and Relevance: This cohort study estimates the prevalence and describes the tumors of MAS. Additional studies are needed in genetically diverse populations to further define population prevalence and disease phenotypes.</p>
18 Keywords
- Aged
- Astrocytoma
- Brain Neoplasms
- Cohort Studies
- Cyclin-Dependent Kinase Inhibitor p16
- Female
- Humans
- Male
- Melanoma
- Melanoma, Cutaneous Malignant
- Middle Aged
- Nervous System Neoplasms
- Neurilemmoma
- Neurofibromatosis 1
- Phenotype
- Prevalence
- Retrospective Studies
- Skin Neoplasms
22 Authors
- Michael R. Sargen
- Jung Kim
- Thomas P. Potjer
- Mary E. Velthuizen
- Arelis E. Martir-Negron
- Yazmin Odia
- Hildur Helgadottir
- Jessica N. Hatton
- Jeremy S. Haley
- Gretchen Thone
- Brigitte C. Widemann
- Andrea M. Gross
- Marielle E. Yohe
- Rosandra N. Kaplan
- Jack F. Shern
- R. Taylor Sundby
- Esteban Astiazaran-Symonds
- Xiaohong R. Yang
- David J. Carey
- Margaret A. Tucker
- Douglas R. Stewart
- Alisa M. Goldstein
1 Application
| Application ID | Title |
|---|---|
| 54389 | Frequency, phenotypic spectrum, and penetrance of pathogenic variation in cancer susceptibility genes in the general population |
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