An updated understanding of follicular lymphoma transformation

Although most patients with follicular lymphoma (FL) follow an indolent disease course, some patients experience a critical inflection point when FL transforms into an aggressive lymphoma. Historically, FL transformation is marked by poor outcomes, particularly for patients with previous FL-directed treatment. Compared with FL, transformed FL (tFL) is marked by numerous additional genetic changes, upregulates novel signaling pathways, and arises from an ancestral FL clone with shared FL-initiating mutations. Prediction of tFL risk remains a high-priority area of disease research, with recent work highlighting memory-like B-cell phenotypes associated with transformation risk and implicating critical tumor-immune interactions at transformation emergence. Mechanistic studies provide insight into the role of genetic drivers in determining malignant B-cell phenotypes or reducing microenvironmental dependencies. In parallel, a shifting therapeutic landscape marked by novel immune-based therapeutics is improving outcomes for patients, yet further clinical outcome data in tFL are greatly needed. This review summarizes recent scientific and clinical studies in tFL and provides an updated understanding of the biological basis, diagnosis, and clinical management of tFL. We conclude with a proposed plan of future research aimed at the goal of increasing tFL biologic knowledge and improving outcomes for patients with tFL.

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Publication Details

Journal
Blood
Published
2025-05-15
DOI
https://doi.org/10.1182/blood.2024026016
Citations
5
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
7.36

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article

An updated understanding of follicular lymphoma transformation

Erin Michelle Parry, Jessica Okosun
5 citations
Blood
Lymphoma Diagnosis and Treatment
7.36
article

An updated understanding of follicular lymphoma transformation

Erin Michelle Parry, Jessica Okosun
article en
5 citations

Abstract

Although most patients with follicular lymphoma (FL) follow an indolent disease course, some patients experience a critical inflection point when FL transforms into an aggressive lymphoma. Historically, FL transformation is marked by poor outcomes, particularly for patients with previous FL-directed treatment. Compared with FL, transformed FL (tFL) is marked by numerous additional genetic changes, upregulates novel signaling pathways, and arises from an ancestral FL clone with shared FL-initiating mutations. Prediction of tFL risk remains a high-priority area of disease research, with recent work highlighting memory-like B-cell phenotypes associated with transformation risk and implicating critical tumor-immune interactions at transformation emergence. Mechanistic studies provide insight into the role of genetic drivers in determining malignant B-cell phenotypes or reducing microenvironmental dependencies. In parallel, a shifting therapeutic landscape marked by novel immune-based therapeutics is improving outcomes for patients, yet further clinical outcome data in tFL are greatly needed. This review summarizes recent scientific and clinical studies in tFL and provides an updated understanding of the biological basis, diagnosis, and clinical management of tFL. We conclude with a proposed plan of future research aimed at the goal of increasing tFL biologic knowledge and improving outcomes for patients with tFL.

BloodVol. 146(15)
Broad Institute (US), St Bartholomew's Hospital (GB), Harvard University (US), Queen Mary University of London (GB), Dana-Farber Cancer Institute (US)
Damon Runyon Cancer Research Foundation, AstraZeneca, Queen Mary University of London, BeiGene, Incyte, Cancer Research UK, National Institute for Health and Care Research, Eisai, St George's University Hospitals NHS Foundation Trust, Barts Health NHS Trust, National Institutes of Health, National Cancer Institute
Openalex Percentile: Top 3%
Lymphoma Diagnosis and Treatment
7.36
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