Evidence map›Paper›PMID 42329588›Full record

ArticleOncology and therapy2026

Real-World Outcomes Among Medicare Beneficiaries Treated with Bruton Tyrosine Kinase Inhibitors for Treatment-Naïve CLL.

Daniel A Ermann, Deborah M Stephens, Xiaoliang Wang, Irene Varghese, Heidi De Souza, Caitlin Sheetz, Qianhong Fu, Gregory A Maglinte, Rhys Williams, Erlene K Seymour and 3 more

Abstract read
In one paragraph

Article in Oncology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited 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

13 authors.

Daniel A ErmannHuntsman Cancer Institute, University of Utah School of Medicine, Salt Lake City, UT, USA. daniel.ermann@hci.utah.edu.
Deborah M StephensUniversity of North Carolina School of Medicine, Chapel Hill, NC, USA.
Xiaoliang WangBeOne Medicines, Ltd, San Carlos, CA, USA.
Irene VargheseADVI Health, Washington, DC, USA.
Heidi De SouzaADVI Health, Washington, DC, USA.
Caitlin SheetzADVI Health, Washington, DC, USA.
Qianhong FuBeOne Medicines, Ltd, San Carlos, CA, USA.
Gregory A MaglinteBeOne Medicines, Ltd, San Carlos, CA, USA.
Rhys WilliamsBeOne Medicines, Ltd, San Carlos, CA, USA.
Erlene K SeymourBeOne Medicines, Ltd, San Carlos, CA, USA.
Derrick van BeugeBeOne Medicines, Ltd, San Carlos, CA, USA.
Mazyar ShadmanFred Hutchinson Cancer Center, University of Washington, Seattle, WA, USA.
Ryan JacobsAtrium Health Levine Cancer Institute, Wake Forest University School of Medicine, Charlotte, NC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThere is a dearth of head-to-head studies comparing covalent Bruton tyrosine kinase (cBTK) inhibitors in adults with chronic lymphocytic leukemia (CLL). Real-world evidence may complement clinical trial data by assessing relative effectiveness in routine practice. This retrospective observational study used a de-identified Medicare Fee-For-Service database to compare real-world outcomes associated with first-line cBTKi monotherapies in older adults with CLL.

methodsPatients aged ≥ 65 years with CLL initiating first-line ibrutinib, acalabrutinib, or zanubrutinib monotherapy between January 1, 2020 and September 30, 2025 were included. Real-world time to treatment discontinuation (rwTTD), time to next treatment (rwTTNT), and overall survival (rwOS) were evaluated using Kaplan-Meier analyses and Cox proportional hazards models. Subgroup analyses were performed by age group.

resultsAmong 10,523 patients included, 3006 (28.6%) received zanubrutinib (median follow-up 15.8 months), 4309 (40.9%) received acalabrutinib (20.7 months), and 3208 (30.5%) received ibrutinib (34.9 months). Median rwTTD was not reached (NR) for zanubrutinib, compared with 24 months for acalabrutinib and 14 months for ibrutinib. Median rwTTNT was NR for zanubrutinib, 40 months for acalabrutinib, and 20 months for ibrutinib. After adjustments for age, sex, race, CCI, and year of index, zanubrutinib had significantly longer rwTTD (hazard ratio [HR] 0.57 [95% CI 0.51-0.61]), rwTTNT (HR 0.63 [0.55-0.71]), and rwOS (HR 0.64 [0.54-0.77]) compared to ibrutinib. Zanubrutinib also had significantly improved rwTTD (HR 0.86 [0.78-0.94]), rwTTNT (HR 0.87 [0.78-0.96]), and rwOS (HR 0.77 [0.66-0.88]) compared to acalabrutinib. Similar patterns were observed when stratified by age group over 65.

conclusionsThese findings demonstrate that zanubrutinib is associated with improved real-world outcomes compared with other cBTK inhibitors.

Indexed as

AcalabrutinibBTK inhibitorChronic lymphocytic leukemiaIbrutinibReal-world outcomesZanubrutinib

Identifiers

PMID42329588
PMCPMC13574742

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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.