Evidence map›Paper›PMID 39594670›Full record

ReviewCells2024

BCL2i-Based Therapies and Emerging Resistance in Chronic Lymphocytic Leukemia.

Wing Fai Li, Eleftheria Atalla, Jiaxin Dong, Marina Konopleva

Abstract readReview
In one paragraph

Review in Cells, 2024. 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. Article
  3. Review
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

4 authors.

Wing Fai LiDepartment of Internal Medicine, Jacobi Medical Center, Bronx, NY 10461, USA.
Eleftheria AtallaDepartment of Hematology and Oncology, The University of Texas at San Antonio, San Antonio, TX 78249, USA.
Jiaxin DongDepartment of Oncology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Marina KonoplevaDepartment of Oncology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.ORCID 0000-0002-9347-2212

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of the anti-apoptotic protein BCL-2 is a key factor in the pathogenesis of chronic lymphocytic leukemia (CLL) and is associated with poor clinical outcomes. Therapeutic activation of apoptosis in cancer cells using the BCL-2 inhibitor (BCL2i) venetoclax has shown remarkable efficacy in clinical trials, both as monotherapy and combination regimens. However, patients with CLL experience a highly variable clinical course, facing significant challenges in advanced stages due to disease relapse and the emergence of resistant clones. Resistance mechanisms include acquired

Indexed as

Drug Resistance, NeoplasmLeukemia, Lymphocytic, Chronic, B-CellProto-Oncogene Proteins c-bcl-2Antineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicHumansSulfonamidesAntineoplastic AgentsBCL2 protein, humanBridged Bicyclo Compounds, HeterocyclicProto-Oncogene Proteins c-bcl-2SulfonamidesvenetoclaxBCL2ichronic lymphocytic leukemiaclinical trialsdrug resistancevenetoclax

Identifiers

PMID39594670
PMCPMC11592612

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.