Evidence map›Paper›PMID 39193190›Full record

ArticleHemaSphere2024

Long-term immune changes in patients with relapsed/refractory chronic lymphocytic leukemia following treatment with venetoclax plus rituximab.

Arnon P Kater, Barbara F Eichhorst, Carolyn J Owen, Ulrich Jaeger, Brenda Chyla, Marcus Lefebure, Rosemary Millen, Yanwen Jiang, Maria Thadani-Mulero, Michelle Boyer and 1 more

Registry-linked trialAbstract read
In one paragraph

Article in HemaSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02005471 (A Multicenter, Phase III, Open-Label, Randomized Study in Relapsed/Refractory Patients With Chronic Lymphocytic Leukemia to Evaluate the Benefit of Venetoclax), which is not on this 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.

NCT02005471 phase3completednot on this map

A Multicenter, Phase III, Open-Label, Randomized Study in Relapsed/Refractory Patients With Chronic Lymphocytic Leukemia to Evaluate the Benefit of Venetoclax (GDC-0199/ABT-199) Plus Rituximab Compared With Bendamustine Plus Rituximab

TypeinterventionalSponsorHoffmann-La RocheRan2014 to 2022Enrolled389ConditionsChronic Lymphocytic LeukemiaArmsBendamustine, Venetoclax, Rituximab
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
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.

Arnon P KaterDepartment of Hematology, Cancer Center Amsterdam, LYMMCARE, Amsterdam University Medical Centers University of Amsterdam Amsterdam The Netherlands.
Barbara F EichhorstDepartment of Internal Medicine and Center of Integrated Oncology Aachen, Bonn, Cologne, Dusseldorf (CIO ABCD), Faculty of Medicine and University Hospital Cologne University of Cologne Cologne Germany.
Carolyn J OwenDepartments of Medicine and Oncology University of Calgary Calgary Alberta Canada.
Ulrich JaegerClinical Department of Hematology and Hemostaseology Medical University of Vienna Vienna Austria.
Brenda ChylaAbbVie North Chicago Illinois USA.
Marcus LefebureRoche Products Ltd Welwyn Garden City UK.
Rosemary MillenRoche Products Ltd Welwyn Garden City UK.
Yanwen JiangGenentech Inc. South San Francisco California USA.
Maria Thadani-MuleroRoche Products Ltd Welwyn Garden City UK.
Michelle BoyerRoche Products Ltd Welwyn Garden City UK.
John F SeymourPeter MacCallum Cancer Centre Royal Melbourne Hospital and University of Melbourne Melbourne Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune dysregulation is a hallmark of chronic lymphocytic leukemia (CLL). Anti-CD20 antibodies (e.g., rituximab [R]) can be combined with venetoclax (Ven) to treat CLL. However, anti-CD20 antibodies can increase hypogammaglobulinemia risk, while the effects of Ven on immune dysregulation are still uncertain. We report long-term immune changes in VenR- and bendamustine-R (BR)-treated patients with relapsed/refractory CLL in the MURANO trial (NCT02005471). Patients were randomized to fixed-duration VenR (2 years Ven; VenR for the first 6 months) or BR (6 months). Immune cell levels were evaluated at the end of combination treatment (EOCT), end of treatment (EOT; VenR arm only), and 12 and 24 months post-EOCT. Overall, 130/194 VenR- and 134/195 BR-treated patients completed treatment without progressive disease. In patients who completed VenR combination therapy, median immunoglobulin (Ig)G and IgM levels decreased from baseline to EOT (

Identifiers

PMID39193190
PMCPMC11347997

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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 Socratic graph.