ERBB2/ ERBB3-mutated S100/ SOX10-positive unclassified high-grade uterine sarcoma: first detailed description of a novel entity
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, kazuistiky
PubMed
39196362
PubMed Central
PMC11564289
DOI
10.1007/s00428-024-03908-3
PII: 10.1007/s00428-024-03908-3
Knihovny.cz E-zdroje
- Klíčová slova
- EGFR, Molecular profiling; nerve sheath tumor, Targeted therapy, Tyrosine kinase fusions, Undifferentiated uterine sarcoma,
- MeSH
- lidé středního věku MeSH
- lidé MeSH
- mutace * MeSH
- nádorové biomarkery genetika MeSH
- nádory dělohy * genetika patologie MeSH
- proteiny S100 genetika metabolismus MeSH
- receptor erbB-2 * genetika MeSH
- receptor erbB-3 * genetika MeSH
- sarkom * genetika patologie MeSH
- stupeň nádoru MeSH
- transkripční faktory SOXE * genetika MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- Názvy látek
- ERBB2 protein, human MeSH Prohlížeč
- ERBB3 protein, human MeSH Prohlížeč
- nádorové biomarkery MeSH
- proteiny S100 MeSH
- receptor erbB-2 * MeSH
- receptor erbB-3 * MeSH
- SOX10 protein, human MeSH Prohlížeč
- transkripční faktory SOXE * MeSH
With the increasing use of innovative next generation sequencing (NGS) platforms in routine diagnostic and research settings, the genetic landscape of uterine sarcomas has been dynamically evolving during the last two decades. Notably, the majority of recently recognized genotypes in uterine sarcomas represent gene fusions, while recurrent oncogene mutations of diagnostic and/ or therapeutic value have been rare. Recently, a distinctive aggressive uterine sarcoma expressing S100 and SOX10, but otherwise lacking diagnostic morphological, immunophenotypic and molecular features of other uterine malignancies has been presented in a scientific abstract form (USCAP, 2023), but detailed description and delineation of the entity is still missing. We herein describe two high-grade unclassified uterine sarcomas characterized by spindle to round cell morphology and diffuse expression of S100 and SOX10, originating in the uterine body and cervix of 53- and 45-year-old women and carrying an ERBB3 (p.Glu928Gly) and an ERBB2 (p.Val777Leu) mutation, respectively. Both tumors harbored in addition genomic HER2 amplification, ATRX mutation and CDKN2A deletion. Methylation studies revealed a methylome most similar to MPNST-like tumors, but distinct from melanoma, MPNST, clear cell sarcoma, and endometrial stromal sarcoma. Case 1 died of progressive peritoneal metastases after multiple trials of chemotherapy 47 months after diagnosis. Case 2 is a recent case who presented with a cervical mass, which was biopsied. This study defines a novel heretofore unrecognized aggressive uterine sarcoma with unique phenotypic and genotypic features. Given the potential value of targeting HER2, recognizing this tumor type is mandatory for appropriate therapeutic strategies and for better future delineation of the entity.
Biotical Laboratory Ltd Plzeň Czech Republic
Comprehensive Cancer Center European Metropolitan Area Erlangen Nuremberg Erlangen Germany
Department of Pathology and Laboratory Medicine Cleveland Clinic Cleveland Ohio USA
Department of Pathology Faculty of Medicine in Plzeň Charles University Plzeň Czech Republic
Department of Pathology The Johns Hopkins University School of Medicine Baltimore Maryland USA
School of Medicine Johannes Kepler University Linz Linz Austria
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