The fifth edition of the WHO classification of mature B‐cell neoplasms: open questions for research

Author:

Coupland Sarah E1,Du Ming‐Qing2ORCID,Ferry Judith A3,de Jong Daphne4,Khoury Joseph D5,Leoncini Lorenzo6,Naresh Kikkeri N7,Ott German8,Siebert Reiner9,Xerri Luc10,

Affiliation:

1. Liverpool Clinical Laboratories Liverpool University Hospitals Foundation Trust Liverpool UK

2. Department of Pathology University of Cambridge Cambridge UK

3. Department of Pathology Massachusetts General Hospital and Harvard Medical School Boston MA USA

4. The Netherlands Cancer Institute Amsterdam The Netherlands

5. Department of Pathology, Microbiology and Immunology University of Nebraska Medical Center Omaha NE USA

6. Department of Medical Biotechnology University of Siena Siena Italy

7. Department of Laboratory Medicine and Pathology University of Washington Seattle WA USA

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

9. Institute of Human Genetics Ulm University and Ulm University Medical Center Ulm Germany

10. Institut Paoli‐Calmettes CRCM and Aix‐Marseille University Marseille France

Abstract

AbstractThe fifth edition of the World Health Organization Classification of Haematolymphoid Tumours (WHO‐HAEM5) is the product of an evidence‐based evolution of the revised fourth edition with wide multidisciplinary consultation. Nonetheless, while every classification incorporates scientific advances and aims to improve upon the prior version, medical knowledge remains incomplete and individual neoplasms may not be easily subclassified in a given scheme. Thus, optimal classification requires ongoing study, and there are certain aspects of some entities and subtypes that require further refinements. In this review, we highlight a selection of these challenging areas to prompt more research investigations. These include (1) a ‘placeholder term’ of splenic B‐cell lymphoma/leukaemia with prominent nucleoli (SBLPN) to accommodate many of the splenic lymphomas previously classified as hairy cell leukaemia variant and B‐prolymphocytic leukaemia, a clear new start to define their pathobiology; (2) how best to classify BCL2 rearrangement negative follicular lymphoma including those with BCL6 rearrangement, integrating the emerging new knowledge on various germinal centre B‐cell subsets; (3) what is the spectrum of non‐IG gene partners of MYC translocation in diffuse large B‐cell lymphoma/high‐grade B‐cell lymphoma and how they impact MYC expression and clinical outcome; how best to investigate this in a routine clinical setting; and (4) how best to define high‐grade B‐cell lymphoma not otherwise specified and high‐grade B‐cell lymphoma with 11q aberrations to distinguish them from their mimics and characterise their molecular pathogenetic mechanism. Addressing these questions would provide more robust evidence to better define these entities/subtypes, improve their diagnosis and/or prognostic stratification, leading to better patient care. © 2024 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Funder

Blood Cancer UK

Cancer Research UK

Publisher

Wiley

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