Progression of follicular lymphoma and related entities: Report from the 2021 SH/EAHP Workshop

Author:

Duffield Amy S1,Dogan Ahmet1,Amador Catalina2,Cook James R3ORCID,Czader Magdalena4,Goodlad John R5,Nejati Reza6,Xiao Wenbin1ORCID,Happ Lanie7,Parker Clay7,Thacker Elizabeth7,Thakkar Devang8,Dave Sandeep S8,Wasik Mariusz A6ORCID,Ott German9

Affiliation:

1. Department of Pathology and Laboratory Medicine, Hematopathology Service, Memorial Sloan Kettering Cancer Center , New York, NY , US

2. Department of Pathology and Laboratory Medicine, University of Miami Miller School of Medicine , Miami, FL , US

3. Department of Laboratory Medicine, Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic , Cleveland, OH , US

4. Department of Pathology and Laboratory Medicine, Indiana University School of Medicine , Indianapolis, IN , US

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

6. Department of Pathology, Fox Chase Cancer Center , Philadelphia, PA , US

7. Data Drive Bioscience , Durham, NC , US

8. Center for Genomic and Computational Biology and Department of Medicine, Duke University , Durham, NC , US

9. Abteilung für Klinische Pathologie, Robert-Bosch-Krankenhaus, and Dr Margarete Fischer-Bosch Institut für Klinische Pharmakologie , Stuttgart , Germany

Abstract

Abstract Objectives The 2021 Society for Hematopathology and European Association for Haematopathology Workshop addressed the molecular and cytogenetic underpinnings of transformation and transdifferentiation in lymphoid neoplasms. Methods Session 4, “Transformations of Follicular Lymphoma,” and session 5, “Transformations of Other B-Cell Lymphomas,” included 45 cases. Gene alteration analysis and expression profiling were performed on cases with submitted formalin-fixed, paraffin embedded tissue. Results The findings from session 4 suggest that “diffuse large B-cell lymphoma/high-grade B-cell lymphoma with rearrangements of MYC and BCL2” is a distinct category arising from the constraints of a preexisting BCL2 translocation. TdT expression in aggressive B-cell lymphomas is associated with MYC rearrangements, immunophenotypic immaturity, and a dismal prognosis but must be differentiated from lymphoblastic ­lymphoma. Cases in session 5 illustrated unusual morphologic and immunophenotypic patterns of transformation. Additionally, the findings support the role of cytogenetic abnormalities—specifically, MYC and NOTCH1 rearrangements—as well as single gene alterations, including TP53, in transformation. Conclusions Together, these unique cases and their accompanying molecular and cytogenetic data suggest potential mechanisms for and unusual patterns of transformation in B-cell lymphomas and indicate numerous opportunities for further study.

Funder

National Cancer Institute

National Institutes of Health

Robert-Bosch-Stiftung, Stuttgart

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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