Evidence map›Paper›PMID 42120657›Full record

ArticleAnnals of hematology2026

Comparable outcomes of BTK inhibitors and fixed-duration venetoclax plus rituximab in second-line treatment of chronic lymphocytic leukaemia: a real-world analysis by the Czech CLL study group.

Jana Mihályová, Anna Panovská, Martin Šimkovič, Lukáš Smolej, Martin Špaček, Tereza Shokralla, Zuzana Kubová, Jana Zuchnická, Tomáš Arpáš, Pavel Vodárek and 7 more

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in Annals of hematology, 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

17 authors.

Jana MihályováDepartment of Hematooncology, University Hospital Ostrava, Ostrava, Czech Republic. jana.mihalyova@fno.cz.ORCID http://orcid.org/0000-0001-6773-7873
Anna PanovskáDepartment of Internal Medicine - Hematology and Oncology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID http://orcid.org/0000-0003-4955-3039
Martin Šimkovič4th Department of Internal Medicine-Hematology, Faculty of Medicine in Hradec Králové, University Hospital and Charles University in Prague, Hradec Králové, Czech Republic.ORCID http://orcid.org/0000-0003-0331-5334
Lukáš Smolej4th Department of Internal Medicine-Hematology, Faculty of Medicine in Hradec Králové, University Hospital and Charles University in Prague, Hradec Králové, Czech Republic.ORCID http://orcid.org/0000-0002-4187-8595
Martin Špaček1st Department of Medicine - Haematology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.ORCID http://orcid.org/0000-0001-5250-8218
Tereza Shokralla1st Department of Medicine - Haematology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Zuzana KubováDepartment of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University and University Hospital, Olomouc, Czech Republic.
Jana ZuchnickáDepartment of Hematooncology, University Hospital Ostrava, Ostrava, Czech Republic.
Tomáš ArpášDepartment of Internal Medicine - Hematology and Oncology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID http://orcid.org/0000-0002-5198-0307
Pavel Vodárek4th Department of Internal Medicine-Hematology, Faculty of Medicine in Hradec Králové, University Hospital and Charles University in Prague, Hradec Králové, Czech Republic.ORCID http://orcid.org/0000-0002-8050-7594
Peter TurcsányiDepartment of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University and University Hospital, Olomouc, Czech Republic.ORCID http://orcid.org/0000-0003-0839-3841
Lenka PolcerováInstitute of Biostatistics and Analyses, Ltd, Brno, Czech Republic.ORCID http://orcid.org/0000-0003-3034-9599
Marika ChrápaváInstitute of Biostatistics and Analyses, Ltd, Brno, Czech Republic.
Daniel LysákDepartment of Hematology and Oncology, Medical School and Teaching Hospital in Plzen, Charles University in Prague, Plzen, Czech Republic.ORCID http://orcid.org/0000-0001-9391-4247
Martin BrejchaHospital Agel, Nový Jičín, Czech Republic.
Heidi MócikováDepartment of Hematology, Fakultni nemocnice Kralovske Vinohrady and 3rd Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID http://orcid.org/0000-0003-2034-0769
Michael DoubekDepartment of Internal Medicine - Hematology and Oncology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID http://orcid.org/0000-0002-1269-6282

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In relapsed/refractory (RR) chronic lymphocytic leukaemia (CLL), Bruton tyrosine kinase inhibitors (BTKi) are administered as monotherapy until disease progression. In contrast, venetoclax, a B-cell lymphoma 2 (BCL-2) protein inhibitor, is typically combined with rituximab (VenR) as a time-limited regimen. To date, neither randomized nor retrospective trials have directly compared these approaches in RR CLL, and only limited data are available comparing venetoclax plus obinutuzumab (VenObi) to BTKi in the first-line setting. We retrospectively analysed 352 patients receiving second-line therapy: 93 VenR and 259 BTKi (ibrutinib: n = 222; acalabrutinib: n = 37). Baseline characteristics were well balanced, except for a higher incidence of TP53 mutation and trisomy 12 in BTKi-treated patients. At a median follow-up of 13.8 months (VenR) and 22.1 months (BTKi), 12-month progression-free survival (PFS) and overall survival (OS) were comparable (PFS: 85.1% vs. 82.2%, p = 0.265; OS: 87.6% vs. 88.4%, p = 0.291). Estimated median PFS (45.4 vs. 37.9 months, p = 0.265) and OS (83.6 vs. 74.2 months, p = 0.291) also showed no significant differences between the VenR and BTKi cohorts. Treatment discontinuation due to adverse events before month 24 was more frequent with BTKi (22.5% with VenR vs. 34.3% with BTKi), primarily due to infections (10.6% vs. 28.6%) and disease progression (14.3% vs. 22.5%). These preliminary data suggest comparable outcomes and manageable toxicity profiles for both regimens.

Indexed as

Agammaglobulinaemia Tyrosine KinaseAntineoplastic Combined Chemotherapy ProtocolsLeukemia, Lymphocytic, Chronic, B-CellRituximabSulfonamidesTyrosine Kinase InhibitorsAdenineAgedAged, 80 and overAntibodies, Monoclonal, HumanizedBenzamidesBridged Bicyclo Compounds, HeterocyclicFemaleHumansMaleMiddle AgedacalabrutinibAdenineAgammaglobulinaemia Tyrosine KinaseAntibodies, Monoclonal, HumanizedBenzamidesBridged Bicyclo Compounds, HeterocyclicBTK protein, humanibrutinibobinutuzumabPiperidinesPyrazinesRituximabSulfonamidesTyrosine Kinase InhibitorsvenetoclaxAcalabrutinibChronic lymphocytic leukaemiaIbrutinibRituximabVenetoclax

Identifiers

PMID42120657
PMCPMC13357439

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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.