Evidence map›Paper›PMID 41793237›Full record

ReviewEuropean journal of haematology2026

Management of Primary Refractory Diffuse Large B-Cell Lymphoma in Patients Unsuitable for CAR T-Cell Therapy.

Santino Caserta, Enrica Antonia Martino, Mamdouh Skafi, Maria Eugenia Alvaro, Antonella Bruzzese, Nicola Amodio, Eugenio Lucia, Virginia Olivito, Caterina Labanca, Francesco Mendicino and 3 more

Abstract readReview
In one paragraph

Review in European journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Experimental and therapeutic medicine · 2026
    Article
  2. Review
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Santino CasertaDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.
Enrica Antonia MartinoDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.
Mamdouh SkafiEmergency and Internal Medicine Department, Saint Joseph Hospital, East Jerusalem, Palestine.
Maria Eugenia AlvaroDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.
Antonella BruzzeseDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.
Nicola AmodioDepartment of Experimental and Clinical Medicine, University of Catanzaro, Catanzaro, Italy.
Eugenio LuciaDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.
Virginia OlivitoDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.
Caterina LabancaDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.
Francesco MendicinoDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.ORCID https://orcid.org/0000-0001-6339-632X
Ernesto VignaDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.
Fortunato MorabitoAIL Sezione di Cosenza, Cosenza, Italy.
Massimo GentileDepartment of Onco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.ORCID https://orcid.org/0000-0002-5256-0726

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary refractory Diffuse Large B-Cell Lymphoma is associated with poor outcomes and limited responsiveness to conventional salvage therapies. Although CAR T-cell therapy represents the standard of care in this setting, a substantial proportion of patients cannot receive it despite meeting disease-related criteria. In this review, "unsuitable" refers to patients who are temporarily or functionally unable to undergo CAR T-cell therapy because of reversible clinical conditions, rapidly progressive disease requiring immediate cytoreduction, or logistical and social barriers, rather than permanent contraindications. For these patients, prompt alternative strategies are required. Conventional platinum-based or gemcitabine- and bendamustine-containing regimens retain a role for short-term disease control but offer limited durability. In contrast, novel antibody-based therapies, including polatuzumab-containing combinations, loncastuximab tesirine, and tafasitamab plus lenalidomide, have expanded treatment options with improved tolerability. Most notably, CD20 × CD3 bispecific antibodies represent a major therapeutic advance, providing off-the-shelf immune engagement with predominantly outpatient administration. From a practical perspective, early identification of reversible barriers to CAR T-cell therapy and timely use of bispecific antibodies or other antibody-based regimens are critical to achieve rapid disease control, preserve organ function, and, when feasible, restore eligibility for cellular therapy.

Indexed as

Immunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyDisease ManagementHumansReceptors, Chimeric AntigenSalvage TherapyTreatment OutcomeReceptors, Chimeric Antigenantibody–drug conjugatesbispecific antibodiesCAR T‐cell therapyCAR T‐cell unsuitabilitydisease progressionDLBCLprimary refractory DLBCLsalvage therapy

Identifiers

PMID41793237
PMCPMC13141660

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.