Targeted RNA Sequencing Highlights a Diverse Genomic and Morphologic Landscape in Low-grade Endometrial Stromal Sarcoma, Including Novel Fusion Genes

Author:

Kolin David L.1,Nucci Marisa R.1,Turashvili Gulisa2,Song Sharon J.1,Corbett-Burns Sophie3,Cesari Matthew45,Chang Martin C.6,Clarke Blaise47,Demicco Elizabeth48,Dube Valerie45,Lee Cheng-Han9,Rouzbahman Marjan47,Shaw Patricia410,Cin Paola Dal11,Swanson David8,Dickson Brendan C.48

Affiliation:

1. Department of Pathology, Division of Women’s and Perinatal Pathology

2. Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA

3. Douglass Hanly Moir Pathology, Macquarie Park, New South Wales, Australia

4. Department of Laboratory Medicine and Pathobiology, University of Toronto

5. Department of Pathology, Trillium Health Partners, Mississauga, Ontario

6. Department of Pathology and Laboratory Medicine, University of Vermont Medical Center, Burlington, VT

7. Department of Pathology & Laboratory Medicine, University Health Network

8. Department of Pathology and Laboratory Medicine, Mount Sinai Hospital

9. Laboratory Medicine & Pathology Department, University of Alberta, Edmonton, Alberta, Canada

10. Department of Anatomic Pathology, Sunnybrook Health Sciences Centre, Toronto

11. Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA

Abstract

Low-grade endometrial stromal sarcoma (LGESS) represents a morphologically and genetically heterogenous mesenchymal neoplasm. Previous work has shown that approximately half of LGESS are characterized by JAZF1::SUZ12 gene fusions, while a smaller proportion involves rearrangement of other genes. However, a subset of cases has no known genetic abnormalities. To better characterize the genomic landscape of LGESS, we interrogated a cohort with targeted RNA sequencing (RNA-Seq). Cases previously diagnosed as low-grade endometrial stromal neoplasia (n=51) were identified and re-reviewed for morphology and subjected to RNA-Seq, of which 47 were successfully sequenced. The median patient age was 49 years (range: 19 to 85). The most commonly detected fusions were JAZF1::SUZ12 (n=26, 55%) and BRD8::PHF1 (n=3, 6%). In addition to the usual/typical LGESS morphology, some JAZF1::SUZ12 fusion tumors showed other morphologies, including fibrous, smooth muscle, sex-cord differentiation, and myxoid change. Novel translocations were identified in 2 cases: MEAF6::PTGR2 and HCFC1::PHF1. Ten tumors (21%) had no identifiable fusion, despite a similar morphology and immunophenotype to fusion-positive cases. This suggests that a subset of cases may be attributable to fusion products among genes that are not covered by the assay, or perhaps altogether different molecular mechanisms. In all, these findings confirm that RNA-Seq is a potentially useful ancillary test in the diagnosis of endometrial stromal neoplasms and highlight their diverse morphology.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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