Progression of Hodgkin lymphoma and plasma cell neoplasms: Report from the 2021 SH/EAHP Workshop

Author:

Nejati Reza1,Amador Catalina2,Czader Magdalena3,Thacker Elizabeth4,Thakkar Devang5,Dave Sandeep S5,Dogan Ahmet6,Duffield Amy6,Goodlad John R7,Ott German8,Wasik Mariusz A1ORCID,Xiao Wenbin5ORCID,Cook James R9ORCID

Affiliation:

1. Department of Pathology, Fox Chase Cancer Center , Philadelphia, PA , USA

2. Department of Pathology, University of Miami Miller School of Medicine , Miami, FL , USA

3. Department of Pathology, Indiana University School of Medicine , Indianapolis, IN , USA

4. Data Driven Bioscience (DDB) , Durham, NC , USA

5. Department of Medcine, Duke University School of Medicine , Durham, NC , USA

6. Department of Pathology, Memorial Sloan Kettering Cancer Center , New York, NY , USA

7. Department of Pathology, NHS Greater Glasgow and Clyde , Glasgow , UK

8. Department of Clinical Pathology, Robert-Bosch-Krankenhaus, and Dr Margarete Fischer-Bosch Institute for Clinical Pharmacology , Stuttgart , Germany

9. Department of Laboratory Medicine, Cleveland Clinic , Cleveland, OH , USA

Abstract

Abstract Objectives To summarize cases submitted to the 2021 Society for Hematopathology/European Association for Haematopathology Workshop under the categories of progression of Hodgkin lymphoma, plasmablastic myeloma, and plasma cell myeloma. Methods The workshop panel reviewed 20 cases covered in this session. In addition, whole-exome sequencing (WES) and whole-genome RNA expression analysis were performed on 10 submitted cases, including 6 Hodgkin lymphoma and 4 plasma neoplasm cases. Results The cases of Hodgkin lymphoma included transformed cases to or from various types of B-cell lymphoma with 1 exception, which had T-cell differentiation. The cases of plasma cell neoplasms included cases with plasmablastic progression, progression to plasma cell leukemia, and secondary B-lymphoblastic leukemia. Gene variants identified by WES included some known to be recurrent in Hodgkin lymphoma and plasma cell neoplasm. All submitted Hodgkin lymphoma samples showed 1 or more of these mutations: SOCS1, FGFR2, KMT2D, RIT1, SPEN, STAT6, TET2, TNFAIP3, and ZNF217. Conclusions Better molecular characterization of both of these neoplasms and mechanisms of progression will help us to better understand mechanisms of progression and perhaps develop better prognostic models, as well as identifying novel therapeutic targets.

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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