Updates in the Classification of T-cell Lymphomas and Lymphoproliferative Disorders

Naoki Oishi, Reham Ahmed, Andrew L. Feldman

Research output: Contribution to journalReview articlepeer-review

Abstract

Purpose of Review: Mature T/NK-cell neoplasms comprise a heterogeneous group of diseases with diverse clinical, histopathologic, immunophenotypic, and molecular features. A clinically relevant, comprehensive, and reproducible classification system for T/NK-cell neoplasms is essential for optimal management, risk stratification, and advancing understanding of these diseases. Two classification systems for lymphoid neoplasms were recently introduced: the 5th edition of World Health Organization classification (WHO-HAEM5) and the 2022 International Consensus Classification (ICC). In this review, we summarize the basic framework and updates in the classification of mature T/NK-cell neoplasms. Recent Findings: WHO-HAEM5 and ICC share basic concepts in classification of T/NK-cell neoplasms, emphasizing integration of clinical presentation, pathology, immunophenotype, and genetics. Major updates in both classifications include unifying nodal T-follicular helper-cell lymphomas into a single entity and establishing EBV-positive nodal T/NK-cell lymphoma as a distinct entity. However, some differences exist in taxonomy, terminology, and disease definitions. Summary: The recent classifications of mature T/NK-cell neoplasms are largely similar and provide new insights into taxonomy based on integrated clinicopathologic features.

Original languageEnglish (US)
Pages (from-to)252-263
Number of pages12
JournalCurrent Hematologic Malignancy Reports
Volume18
Issue number6
DOIs
StatePublished - Dec 2023

Keywords

  • International Consensus Classification
  • Lymphoproliferative disorder
  • Mature T-cell leukemia
  • NK/T-cell lymphoma
  • T-cell lymphoma
  • World Health Organization

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Cancer Research

Fingerprint

Dive into the research topics of 'Updates in the Classification of T-cell Lymphomas and Lymphoproliferative Disorders'. Together they form a unique fingerprint.

Cite this