Dramatic multifocal osteosarcoma treatment response in the setting of POT1 tumor predisposition syndrome
Evidence suggests that hereditable alterations in telomeric function including POT1 are enriched in sarcoma susceptibility. Furthermore, hereditary tumor predisposition syndromes often increase osteosarcoma risk including a recent report of five patients with POT1-TPD. Multifocal osteosarcoma is rare, but a few retrospective cohorts suggest dismal prognosis. This report details an adolescent male with presumed POT1-TPD who developed synchronous multifocal osteosarcoma exquisitely sensitive to chemotherapy which may represent a unique phenotype for the syndrome.
Authors
- Sara Szabo (ORCID: https://orcid.org/0000-0002-6212-7264)
- Brittany Cooper
- Stephen Gilene
- Joseph G. Pressey (ORCID: https://orcid.org/0000-0003-1816-3281)
- Kristen D'Aquila
Institutions
- Cincinnati Children's Hospital Medical Center (US)
Publication Details
- Journal
- Cancer Genetics
- Published
- 2025-08-25
- DOI
- https://doi.org/10.1016/j.cancergen.2025.08.008
- Primary Topic
- Histiocytic Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00