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Paired tumor-normal sequencing provides insights into the CDKN2A-associated tumor spectrum.


ABSTRACT: Germline pathogenic variants (PV) in CDKN2A are characterized by an increased risk for melanoma, pancreatic cancer, nervous system tumors, and additional cancer types. We sought to define the tumor and clinical characteristics in a cohort of cancer patients with CDKN2A PV. Amongst 71,868 patients, 69 (0.1%) had a CDKN2A PV. Of these, 87.0% (n = 60), 7.2% (n = 5), and 5.8% (n = 4) had a PV impacting p16INK4A, p14ARF, or both p16INK4A and p14ARF, respectively. Biallelic inactivation of CDKN2A was observed in 33/47 (70.2%) of tumors assessed. Most tumors (28/38, 73.7%) in patients with p16INK4A PV demonstrated biallelic inactivation, including non-classic tumors such as lung cancer and osteosarcoma. Approximately half (5/9, 55.6%) of tumo

SUBMITTER: Breen KE 

PROVIDER: S-EPMC12630871 | biostudies-literature | 2025 Nov

REPOSITORIES: biostudies-literature