Progression and transformation of chronic lymphocytic leukemia/small lymphocytic lymphoma and B-cell prolymphocytic leukemia: Report from the 2021 SH/EAHP Workshop

Author:

Czader Magdalena1,Amador Catalina2,Cook James R3ORCID,Thakkar Devang4,Parker Clay5,Dave Sandeep S4,Dogan Ahmet6,Duffield Amy S7,Nejati Reza8,Ott German9,Xiao Wenbin6ORCID,Wasik Mariusz8ORCID,Goodlad John R10

Affiliation:

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

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

3. Department of Laboratory Medicine, Cleveland Clinic , Cleveland, OH , US

4. Department of Medicine, Duke University School of Medicine , Durham, NC , US

5. Data Driven Bioscience , Durham, NC , US

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

7. Department of Pathology and Laboratory Medicine, Icahn School of Medicine at Mount Sinai Hospital , New York, NY , US

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

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

10. NHS Greater Glasgow and Clyde , Glasgow , UK

Abstract

Abstract Objectives Session 3 of the 2021 Workshop of the Society for Hematopathology/European Association for Haematopathology examined progression and transformation of chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) and B-cell prolymphocytic leukemia (B-PLL). Methods Thirty-one cases were reviewed by the panel. Additional studies such as immunohistochemistry and molecular genetic testing, including whole-exome sequencing and expression profiling, were performed in select cases. Results Session 3 included 27 CLL/SLL cases and miscellaneous associated proliferations, 3 cases of B-PLL, and 1 case of small B-cell lymphoma. The criteria for ­accelerated CLL/SLL are established for lymph nodes, but extranodal disease can be diagnostically challenging. Richter transformation (RT) is a broad term and includes true transformation from original CLL/SLL clone(s) and clonally unrelated neoplasms. The morphologic, immunophenotypic, and genetic spectrum is diverse with classical and highly unusual examples. T-cell proliferations can also be encountered in CLL/SLL. B-cell prolymphocytic leukemia is a rare, diagnostically challenging disease due to its overlaps with other lymphoid neoplasms. Conclusions The workshop highlighted complexity of progression and transformation in CLL/SLL and B-PLL, as well as diagnostic caveats accompanying heterogeneous presentations of RT and other manifestations of disease progression. Molecular genetic studies are pivotal for diagnosis and determination of clonal relationship, and to predict response to treatment and identify resistance to targeted therapy.

Funder

National Cancer Institute

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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