Evidence map›Paper›PMID 41698679›Full record

ArticleEuropean journal of haematology2026

Real-World Selection of Venetoclax-Obinutuzumab Versus BTK Inhibitor Therapy for Treatment-Naïve Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma.

Rebecca Tidswell, Carolyn Owen, Mona Shafey, Sarah Perry, Nanette Cox-Kennett, Russell Sterrett, Anthea Peters, Robert Puckrin

Abstract read
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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
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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

8 authors.

Rebecca TidswellArthur Child Comprehensive Cancer Centre, Calgary, Canada.
Carolyn OwenArthur Child Comprehensive Cancer Centre, Calgary, Canada.ORCID https://orcid.org/0000-0003-4110-1708
Mona ShafeyArthur Child Comprehensive Cancer Centre, Calgary, Canada.
Sarah PerryArthur Child Comprehensive Cancer Centre, Calgary, Canada.
Nanette Cox-KennettCross Cancer Institute, Edmonton, Canada.
Russell SterrettCross Cancer Institute, Edmonton, Canada.
Anthea PetersCross Cancer Institute, Edmonton, Canada.
Robert PuckrinArthur Child Comprehensive Cancer Centre, Calgary, Canada.ORCID https://orcid.org/0000-0002-8918-6598

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNovel targeted agents have transformed the treatment of chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), including continuous BTK inhibitor (BTKi) therapy and time-limited regimens such as venetoclax-obinutuzumab (Ven-O) and ibrutinib-venetoclax (I + V). However, factors guiding first-line treatment decisions in routine practice remain poorly defined.

objectivesTo describe real-world first-line treatment patterns and identify factors associated with therapy selection.

methodsThis retrospective, population-based study included consecutive patients initiating first-line therapy for CLL/SLL in 2024 in Alberta, Canada.

resultsAmong 148 patients with median age 71 years, time-limited targeted therapy was selected for 75 (51%), including Ven-O (n = 73) and I + V (n = 2). Continuous BTKi therapy was used in 65 (44%), while chemotherapy-based regimens were uncommon (n = 8, 5%). Among 138 patients treated with either continuous BTKi or Ven-O, BTKi use was significantly more frequent among those with del(17p)/TP53 mutation (84% vs. 16%, p = 0.0002), age > 75 years (66% vs. 34%, p = 0.0051), and residence > 100 km from an obinutuzumab-initiating cancer center (70% vs. 30%, p = 0.031).

conclusionsTime-limited and continuous targeted therapies are used with similar frequency for CLL/SLL, with selection shaped by age, TP53 aberrations, geography, and patient preferences. These findings highlight the importance of personalized care and the need to reduce access barriers to time-limited strategies.

Indexed as

Agammaglobulinaemia Tyrosine KinaseAntineoplastic Combined Chemotherapy ProtocolsLeukemia, Lymphocytic, Chronic, B-CellProtein Kinase InhibitorsAgedAged, 80 and overAntibodies, Monoclonal, HumanizedBridged Bicyclo Compounds, HeterocyclicFemaleHumansMaleMiddle AgedRetrospective StudiesSulfonamidesTreatment OutcomeAgammaglobulinaemia Tyrosine KinaseAntibodies, Monoclonal, HumanizedBridged Bicyclo Compounds, HeterocyclicBTK protein, humanobinutuzumabProtein Kinase InhibitorsSulfonamidesvenetoclaxBTK inhibitorschronic lymphocytic leukemiacontinuous therapyobinutuzumabsmall lymphocytic lymphomatime‐limited therapyvenetoclax

Identifiers

PMID41698679
PMCPMC13141657

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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.