Newly diagnosed and relapsed follicular lymphoma: EHA Clinical Practice Guidelines for diagnosis, treatment, and follow-up
In brief
Follicular lymphoma survival likely exceeds 20 years, with treatment tailored to disease burden
European guidelines say median survival after follicular lymphoma diagnosis likely exceeds 20 years, but treatment depends on disease extent and tumor burden. They recommend surveillance for many low-burden cases and different therapies for advanced or relapsed disease, with biopsy and PET-CT central to diagnosis and staging. The long course and risk of relapse make shared decisions and careful follow-up essential.
- Journal
- HemaSphere (Q1)
- Published
- 19 October 2026
- Study design
- Practice guideline / consensus
- Evidence level
- Level 1, High (CEBM 1c)
- Authors
- Marco Ladetto, Natacha Bolaños, Guy Bouguet, Klaus Herfarth, Wolfram Klapper, Sirpa Leppa, et al.
- PMID
- 42903357
- DOI
- 10.1002/hem3.70507
Why clinicians should know about it
- Picked for Hematology (top studies of the week, 25 October 2026): EHA guideline covers follicular lymphoma diagnosis and treatment
Abstract
Follicular lymphoma (FL) is the second most common lymphoma subtype in Europe, with a median age at diagnosis of 60-65 years. It is generally considered an indolent disease, and the median overall survival at diagnosis now likely exceeds 20 years. However, considerable heterogeneity exists. Diagnosis requires adequate biopsy material and a specialized hematopathologist. Staging and prognosis rely on positron emission tomography (PET)-computed tomography (CT). Prognostication at diagnosis is based on several validated clinical prognostic scores. Localized disease is usually treated with radiotherapy ± Rituximab. The treatment of disseminated disease includes active surveillance (or in selected cases Rituximab monotherapy) for low-tumor burden patients, and most often immunochemotherapy (or in selected cases chemo-free therapeutic options), ±antibody maintenance in high-tumor burden patients. For relapsed or refractory disease, treatment with Rituximab-Lenalidomide combination ± Tafasitamab or Epcoritamab from the first relapse and single-agent bispecific antibodies, chimeric antigen receptor T-cell therapy (CAR-T) cells, and Zanubrutinib-Obinutuzumab after second relapse should be prioritized over immunochemotherapy. Given the long natural history and risk of relapse, careful follow-up is an important part of patient management. Patients should be actively involved in decision-making. In this guideline, we present current evidence-based recommendations for diagnosis, staging, treatment, and follow-up.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.