EWSR1::POU2AF3(COLCA2) Sarcoma: An Aggressive, Polyphenotypic Sarcoma With a Head and Neck Predilection
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
37742928
DOI
10.1016/j.modpat.2023.100337
PII: S0893-3952(23)00242-9
Knihovny.cz E-resources
- Keywords
- COLCA2, EWSR1::POU2AF3, gene fusion, neuroendocrine-like, sarcoma, sinonasal tract, soft tissues, spindle cell sarcoma,
- MeSH
- Adult MeSH
- In Situ Hybridization, Fluorescence MeSH
- Middle Aged MeSH
- Humans MeSH
- Biomarkers, Tumor genetics metabolism MeSH
- Soft Tissue Neoplasms * genetics therapy pathology MeSH
- RNA-Binding Protein EWS genetics metabolism MeSH
- Calmodulin-Binding Proteins genetics MeSH
- RNA-Binding Proteins genetics MeSH
- Sarcoma * genetics MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- EWSR1 protein, human MeSH Browser
- Biomarkers, Tumor MeSH
- RNA-Binding Protein EWS MeSH
- Calmodulin-Binding Proteins MeSH
- RNA-Binding Proteins MeSH
EWSR1::POU2AF3 (COLCA2) sarcomas are a recently identified group of undifferentiated round/spindle cell neoplasms with a predilection for the head and neck region. Herein, we report our experience with 8 cases, occurring in 5 men and 3 women (age range, 37-74 years; median, 60 years). Tumors involved the head/neck (4 cases), and one each the thigh, thoracic wall, fibula, and lung. Seven patients received multimodal therapy; 1 patient was treated only with surgery. Clinical follow-up (8 patients; range, 4-122 months; median, 32 months) showed 5 patients with metastases (often multifocal, with a latency ranging from 7 to 119 months), and 3 of them also with local recurrence. The median local recurrence-free and metastasis-free survival rates were 24 months and 29 months, respectively. Of the 8 patients, 1 died of an unknown cause, 4 were alive with metastatic disease, 1 was alive with unresectable local disease, and 2 were without disease. The tumors were composed of 2 morphologic subgroups: (1) relatively bland tumors consisting of spindled to stellate cells with varying cellularity and fibromyxoid stroma (2 cases) and (2) overtly malignant tumors composed of nests of "neuroendocrine-appearing" round cells surrounded by spindled cells (6 cases). Individual cases in the second group showed glandular, osteogenic, or rhabdomyoblastic differentiation. Immunohistochemical results included CD56 (4/4 cases), GFAP (5/8), SATB2 (4/6), keratin (AE1/AE3) (5/8), and S100 protein (4/7). RNA sequencing identified EWSR1::POU2AF3 gene fusion in all cases. EWSR1 gene rearrangement was confirmed by fluorescence in situ hybridization in 5 cases. Our findings confirm the head/neck predilection and aggressive clinical behavior of EWSR1::POU2AF3 sarcomas and widen the morphologic spectrum of these rare lesions to include relatively bland spindle cell tumors and tumors with divergent differentiation.
Department for Human Genetics University Hospitals Leuven KU Leuven Leuven Belgium
Department of Internal Medicine Maastricht University Medical Center Maastricht The Netherlands
Department of Laboratory Medicine and Pathology Mayo Clinic Rochester Minnesota
Department of Pathology Hacettepe University Ankara Turkey
Department of Pathology The Johns Hopkins Medical Institutions Baltimore Maryland
Department of Pathology University Hospitals Leuven KU Leuven Leuven Belgium
References provided by Crossref.org
Molecular pathology in diagnosis and prognostication of head and neck tumors