Evidence map›Paper›PMID 40546723›Full record

ArticleBlood neoplasia2025

Real-world characteristics, treatment patterns, and outcomes of patients with 2 or more LOTs for CLL/SLL in the United States.

Matthew S Davids, Jacob Ambrose, Enrico de Nigris, Jennifer Prescott, Siyang Leng, Mohammed Z H Farooqui, Shravanthi R Gandra, Christina M Zettler, Laura L Fernandes, Ching Kun Wang and 1 more

Abstract read
In one paragraph

Article in Blood neoplasia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. BRUIN 313 and 314 Trials Open the Door for Noncovalent Bruton Tyrosine Kinase Inhibition as Initial Therapy for Chronic Lymphocytic Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  3. Article
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

11 authors.

Matthew S DavidsDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Jacob AmbroseCancer Outcomes Research and Evaluation, COTA, Inc, New York, NY.
Enrico de NigrisOutcomes Research, MSD (UK) Limited, London, UK.
Jennifer PrescottEpidemiology, Merck & Co, Inc, Rahway, NJ.
Siyang LengClinical Development, Merck & Co, Inc, Rahway, NJ.
Mohammed Z H FarooquiClinical Development, Merck & Co, Inc, Rahway, NJ.
Shravanthi R GandraOutcomes Research, Merck & Co, Inc, Rahway, NJ.
Christina M ZettlerCancer Outcomes Research and Evaluation, COTA, Inc, New York, NY.
Laura L FernandesCancer Outcomes Research and Evaluation, COTA, Inc, New York, NY.
Ching Kun WangCancer Outcomes Research and Evaluation, COTA, Inc, New York, NY.
Mazyar ShadmanClinical Research Division, Fred Hutchinson Cancer Center and Hematology & Medical Oncology Division at University of Washington, Seattle, WA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of targeted agents for chronic lymphocytic leukemia (CLL) has transformed the treatment paradigm for patients with CLL. Because of this evolving treatment landscape, contemporaneous evidence was needed related to US treatment patterns and outcomes among patients treated in the real-world. Using COTA's electronic health records-based database, we examined characteristics, treatment patterns, and outcomes of patients receiving ≥2 lines of therapy (LOTs). A total of 1283 adult patients with CLL were identified who initiated second LOT (2L) between 1 January 2014 and 30 June 2022. Of those patients, 542 (42.2%) later received third-line (3L) therapy, of whom 228 (42.1%) went on to receive fourth-line (4L) therapy. Overall, >18% of patients died after 2L initiation and before 3L initiation, and more than a quarter died before 4L initiation. Most patients were White (77.7%), male (60.6%), aged ≥65 years (68.8%), and treated in a community practice setting (87.8%). From 2014 to 2023, the use of chemoimmunotherapy in any ≥2L LOT decreased, whereas use of Bruton tyrosine kinase inhibitor and B-cell lymphoma 2 inhibitor therapy increased. Across endpoints, median times to event(s) were generally shorter with each subsequent LOT received, both in the overall population and among patients receiving a given therapy in different LOTs. With a median follow-up time from 2L initiation of 38.0 months, median real-world time to next treatment, progression-free survival, and overall survival was 31.9, 33.8, and 80.1 months, respectively. Despite great advancements in CLL treatments since 2014, unmet need persists for patients receiving late LOT.

Identifiers

PMID40546723
PMCPMC12182857

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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.