Evidence map›Paper›PMID 41986622›Full record

ReviewLeukemia2026

Evolving therapeutic strategies in mantle cell lymphoma: advancements and future directions.

Rita Tavarozzi, Nawar Maher, Gioacchino Catania, Giulia Zacchi, Francesca D'Andrea, Antonella Sofia, Manuela Zanni, Marco Ladetto

Abstract readReview
In one paragraph

Review in Leukemia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. 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

8 authors.

Rita TavarozziDepartment of Translational Medicine, University of Eastern Piedmont, Novara, Italy. rita.tavarozzi@uniupo.it.ORCID http://orcid.org/0000-0003-3696-7806
Nawar MaherDepartment of Translational Medicine, University of Eastern Piedmont, Novara, Italy.ORCID http://orcid.org/0009-0007-9307-1965
Gioacchino CataniaSCDU of Hematology, Azienda Ospedaliera Universitaria SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
Giulia ZacchiSCDU of Hematology, Azienda Ospedaliera Universitaria SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
Francesca D'AndreaSCDU of Hematology, Azienda Ospedaliera Universitaria SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
Antonella SofiaSCDU of Hematology, Azienda Ospedaliera Universitaria SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
Manuela ZanniSCDU of Hematology, Azienda Ospedaliera Universitaria SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
Marco LadettoDepartment of Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mantle cell lymphoma (MCL) is a biologically and clinically heterogeneous B-cell malignancy with a historically poor prognosis. Recent advances have substantially expanded treatment options, particularly through the integration of targeted therapies, chemotherapy-free regimens, and cellular approaches. Frontline treatment now incorporates Bruton's tyrosine kinase inhibitors (BTKi) in combination with chemotherapy and in chemotherapy-free regimens. For patients with relapsed or refractory disease, particularly those previously exposed to BTKi, chimeric antigen receptor T-cell (CAR T) therapies and third-generation BTKi like pirtobrutinib provide highly effective options while several novel agents, including bispecific antibodies (bsAbs), are under investigation. Nevertheless, achieving long-lasting remissions is still a major challenge, especially among high-risk patients. Future directions include optimizing sequencing, refining rational combination therapies, expanding the application of bsAbs, and integrating small molecules and novel immunoconjugates to enhance therapeutic efficacy and long-term outcomes. This review provides an overview of the current and emerging therapies for MCL, highlighting how the integration of biological agents, strategic combinations, and patient-centered approaches are driving the next phase of MCL treatment.

Indexed as

Lymphoma, Mantle-CellAgammaglobulinaemia Tyrosine KinaseAntibodies, BispecificAntineoplastic Combined Chemotherapy ProtocolsHumansMolecular Targeted TherapyProtein Kinase InhibitorsAgammaglobulinaemia Tyrosine KinaseAntibodies, BispecificProtein Kinase Inhibitors

Identifiers

PMID41986622
PMCPMC13149306

What OpenQuestion holds

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Registered trials

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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.