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New ESMO Clinical Practice Guideline for the Diagnosis and Treatment of DLBCL 20251

Produktresumé för våra godkända läkemedel på FASS: 
Breyanzi® (lisokabtagen-maraleucel)  |  Inrebic® (fedratinib)  |  Reblozyl® (luspatercept)  |  Revlimid® (lenalidomid)

Sep 2025

The new ESMO clinical practice guidelines for lymphomas have been published. The guidelines now include all types of lymphomas in one single document. Here we focus only on DLBCL.

A few selected DLBCL recommendations:

  • A baseline electrocardiogram should be carried out on all patients. Echocardiogram (or multi-gated acquisition or gated heart pool scan if echocardiogram unavailable) can be considered for all patients
    and is recommended for older patients and those with cardiovascular risk factors
  • Positron emission tomography (PET)–computed tomography (CT) can be recommended as the standard imaging modality for baseline and response assessment, and can be considered at interim assessment
  • Assessment of the central nervous system (CNS) with contrast-enhanced cranial magnetic resonance imaging (MRI) and cerebrospinal fluid (CSF) examination can be carried out on a case-by-case basis based on clinical risk factors or presentation
  • Assessment of the frail and elderly using the Elderly Prognostic Index can be considered
  • Patients with early disease progression who relapse ≤12 months after completion of first-line treatment should receive CAR-T therapy, if suitable, including Breyanzi (lisocabtagene maraleucel)
  • Patients relapsing after ≥2 prior lines of treatment should also receive CAR-T therapy, if suitable, for which Breyanzi is also recommended as one option

Click here to read the ESMO guidelines (text in english, estimated reading time 15 minutes)

Key message on CAR-T

aRebiopsy at each relapse, where feasible, to confirm DLBCL [V, B]; bAxicabtagene ciloleucel and lisocabtagene maraleucel are FDA and EMA approved for second-line use; cGlofitamab-Gem-Ox is recommended after ≥1 line of therapy, if available [I, A]; dCaution when selecting Pola-BR for patients who may be candidates for CAR-T therapy as a subsequent treatment line. Bendamustine may have an impact on the quality of T-cells; eConsider palliative care at each treatment juncture in appropri ately selected patients [V, B]; fConsider DS 5 PMR as failure of second-line platinum-based immunoChT on a case-by-case basis; gConsider ISRT to initial isolated bulky relapse or residual isolated PET-avid disease pre- or post-ASCT [IV, B]; hAxicabtagene ciloleucel, lisocabtagene maraleucel and tisagenlecleucel are FDA and EMA app roved options for patients who have received ≥2 prior lines of therapy according to availability and patient preference; iEpcoritamab and glofitamab are FDA and EMA approved for patients who have received ≥2 prior lines of therapy; jOption for patients relapsing after second- or third-line CAR-T therapy or relapsing after second-line treatment if CAR-T-unsuitable; kFor selected young, fit patients who relapse post-CAR-T therapy and who obtain a subsequent remission.

New Swedish guidelines on aggressive B-cell lymphomas were presented in April 2025. Please also refer to the Swedish recommendations for additional guidance.2

Referenser
1. Eyre T.A et al, Ann Oncol 2025.
2. Nationellt Vårdprogram Aggressiva B-cellslymfom 2024, Regionala cancercentrum i samverkan

2009-SE-2500012 sep 2025

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