Evidence map›Paper›PMID 41981887›Full record

ArticleEuropean journal of haematology2026

First-Line Treatment of IGHV-Unmutated Chronic Lymphocytic Leukemia: A Network Meta-Analysis of Targeted and Chemoimmunotherapy Regimens.

Santino Caserta, Enrica Antonia Martino, Danilo Lofaro, Ernesto Vigna, Antonella Bruzzese, Francesco Mendicino, Maria Eugenia Alvaro, Caterina Labanca, Eugenio Lucia, Virginia Olivito and 4 more

Abstract readNetwork Meta-Analysis
In one paragraph

Article in European journal of haematology, 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

14 authors.

Santino CasertaHematology Unit, Department of Onco-Hematology, AO of Cosenza, Cosenza, Italy.
Enrica Antonia MartinoHematology Unit, Department of Onco-Hematology, AO of Cosenza, Cosenza, Italy.
Danilo LofaroDepartment of Mathematics and Computer Science, University of Calabria, Rende, Italy.
Ernesto VignaHematology Unit, Department of Onco-Hematology, AO of Cosenza, Cosenza, Italy.
Antonella BruzzeseHematology Unit, Department of Onco-Hematology, AO of Cosenza, Cosenza, Italy.
Francesco MendicinoHematology Unit, Department of Onco-Hematology, AO of Cosenza, Cosenza, Italy.ORCID https://orcid.org/0000-0001-6339-632X
Maria Eugenia AlvaroHematology Unit, Department of Onco-Hematology, AO of Cosenza, Cosenza, Italy.
Caterina LabancaHematology Unit, Department of Onco-Hematology, AO of Cosenza, Cosenza, Italy.
Eugenio LuciaHematology Unit, Department of Onco-Hematology, AO of Cosenza, Cosenza, Italy.
Virginia OlivitoHematology Unit, Department of Onco-Hematology, AO of Cosenza, Cosenza, Italy.
Nicola AmodioDepartment of Experimental and Clinical Medicine, University of Catanzaro, Catanzaro, Italy.
Fortunato MorabitoAIL Sezione di Cosenza, Italy.
Valter GatteiClinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, Italy.
Massimo GentileHematology Unit, Department of Onco-Hematology, 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

Immunoglobulin heavy chain variable region-unmutated (IGHV-U) chronic lymphocytic leukemia (CLL) represents a biologically aggressive subgroup with limited responsiveness to chemoimmunotherapy (CIT). To clarify the comparative effectiveness of available frontline options, we conducted a comprehensive Bayesian network meta-analysis of randomized clinical trials including more than 4500 IGHV-U patients. Targeted therapies consistently outperformed CIT backbones, confirming the minimal benefit of cytotoxic approaches in this population. Acalabrutinib-based regimens, either as monotherapy or combined with obinutuzumab, emerged as the most effective strategies for progression-free survival, followed by other BTK inhibitors and venetoclax-based combinations. Chlorambucil- and Fludarabine-containing regimens ranked lowest. The fixed-duration venetoclax-obinutuzumab regimen also demonstrated strong efficacy, though estimates were less precise due to a smaller evidence base. Overall, heterogeneity was low, model fit was robust, and no statistical evidence was detected. These findings support targeted agents as the preferred first-line treatment for IGHV-U CLL and provide a quantitative framework to guide regimen selection while highlighting the need for head-to-head trials and long-term follow-up to optimize treatment sequencing.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionImmunotherapyLeukemia, Lymphocytic, Chronic, B-CellMutationHumansMolecular Targeted TherapyTreatment OutcomeImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionBruton tyrosine kinase inhibitorsfirst‐line therapyIGHV unmutated CLLnetwork meta‐analysisPRISMA guidelinesprogression‐free survivalvenetoclax‐based therapy

Identifiers

PMID41981887
PMCPMC13326791

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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.