Evidence map›Paper›PMID 42389542›Full record

ReviewFrontiers in immunology2026

Enhancing immunotherapy efficacy in multiple myeloma and chronic lymphocytic leukemia: from combinatorial therapeutic approaches to gut microbiota modulation.

Andrea Adrados, Juan Pérez-Fernández, Roberto García-Vicente, Alba Garrote-de-Barros, Joaquín Martinez-Lopez, María Linares, María Hernández-Sánchez

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Andrea AdradosDepartment of Translational Hematology, Instituto de Investigación Hospital 12 de Octubre (imas12), Hematological Malignancies Clinical Research Unit H12OCNIO, Madrid, Spain.
Juan Pérez-FernándezDepartment of Biochemistry and Molecular Biology, Pharmacy School, Universidad Complutense de Madrid, Madrid, Spain.
Roberto García-VicenteDepartment of Translational Hematology, Instituto de Investigación Hospital 12 de Octubre (imas12), Hematological Malignancies Clinical Research Unit H12OCNIO, Madrid, Spain.
Alba Garrote-de-BarrosDepartment of Translational Hematology, Instituto de Investigación Hospital 12 de Octubre (imas12), Hematological Malignancies Clinical Research Unit H12OCNIO, Madrid, Spain.
Joaquín Martinez-LopezDepartment of Translational Hematology, Instituto de Investigación Hospital 12 de Octubre (imas12), Hematological Malignancies Clinical Research Unit H12OCNIO, Madrid, Spain.
María Linares *Department of Translational Hematology, Instituto de Investigación Hospital 12 de Octubre (imas12), Hematological Malignancies Clinical Research Unit H12OCNIO, Madrid, Spain.
María Hernández-Sánchez *Department of Translational Hematology, Instituto de Investigación Hospital 12 de Octubre (imas12), Hematological Malignancies Clinical Research Unit H12OCNIO, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma and chronic lymphocytic leukemia are among the most common hematological tumors. Although first-line therapies are initially effective, their clinical benefit is frequently compromised by the emergence of acquired drug resistance. In recent years, novel immunotherapies such as checkpoint inhibitors, chimeric antigen receptor T-cells, and bispecific antibodies are showing promising results in preclinical studies, achieving high rates of response and remission in some cases. However, despite these advances, durable responses are not achieved in all patients, and treatment failure, toxicity and resistance remain major clinical challenges. In this review, we have comprehensively examined current strategies aimed at optimizing immunotherapy efficacy through rational combination approaches including novel immunotherapies with established standard-of-care agents as well as emerging treatments. Moreover, we have explored the growing evidence supporting the role of the gut microbiota in both B-cell malignancies, focusing on its influence on disease biology and modulation of immunotherapeutic responses to further improve patient outcomes. Finally, we have addressed the current challenges and future perspectives in the field of immunotherapy in both diseases.

Indexed as

Gastrointestinal MicrobiomeImmunotherapyLeukemia, Lymphocytic, Chronic, B-CellMultiple MyelomaAnimalsCombined Modality TherapyHumansImmune Checkpoint InhibitorsTreatment OutcomeImmune Checkpoint Inhibitorschronic lymphocytic leukemiacombinatorial therapiesgut microbiotaimmunotherapymultiple myeloma

Identifiers

PMID42389542
PMCPMC13318670

What OpenQuestion holds

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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.