Evidence map›Paper›PMID 39214096›Full record

ArticleCancer cell2024

Overcoming clinical BCR-ABL1 compound mutant resistance with combined ponatinib and asciminib therapy.

Christopher A Eide, Diana Brewer, Tao Xie, Anna Reister Schultz, Samantha L Savage, Serena Muratcioglu, Noah Merz, Richard D Press, Thomas O'Hare, Thomas Jacob and 6 more

Abstract readCase ReportsLetter
In one paragraph

Article in Cancer cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Chronic Myeloid Leukemia and the T315IInternational journal of molecular sciences · 2025
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. 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

16 authors.

Christopher A EideDivision of Hematology & Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Diana BrewerDivision of Hematology & Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Tao XieDepartment of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Anna Reister SchultzDivision of Hematology & Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Samantha L SavageDivision of Hematology & Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Serena MuratciogluDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, USA.
Noah MerzDivision of Hematology & Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Richard D PressDepartment of Pathology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Thomas O'HareDivision of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, The University of Utah, Salt Lake City, UT, USA.
Thomas JacobDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
Tania Q VuDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA; Center for Spatial Systems Bioscience, Oregon Health & Science University, Portland, OR, USA.
Cristina E TognonDivision of Hematology & Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Tara A MaceyDivision of Hematology & Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
John KuriyanDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, USA; Department of Chemistry, Vanderbilt College of Arts and Science, Nashville, TN, USA.
Charalampos G KalodimosDepartment of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Brian J DrukerDivision of Hematology & Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA. Electronic address: drukerb@ohsu.edu.

Funding

Structure and functional mechanisms of molecular chaperones and protein kinasesR35GM122462 · NIGMS · UNIVERSITY OF MINNESOTA · PI CHARALAMPOS KALODIMOS · 2017 to 2026
$6.8M
CHRONIC MYELOGENOUS LEUKEMIA AND BCR-ABL SUBSTRATESR01CA065823 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI DRUKER, BRIAN J · 1995 to 2021
$4.7M
Molecular Digital CytoImaging for Leukemia Drug ScreeningR01CA222095 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI MARTIN, JODY, VU, TOTHU Q · 2018 to 2022
$2.9M
NCI NIH HHS R01 CA065823NCI NIH HHS R01 CA222095NIGMS NIH HHS R35 GM122462
6 · The paper itself

Abstract

BCR-ABL1 compound mutations can lead to resistance to ABL1 inhibitors in chronic myeloid leukemia (CML), which could be targeted by combining the ATP-site inhibitor ponatinib and the allosteric inhibitor asciminib. Here, we report the clinical validation of this approach in a CML patient, providing a basis for combination therapy to overcome such resistance.

Indexed as

Drug Resistance, NeoplasmFusion Proteins, bcr-ablImidazolesLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMutationProtein Kinase InhibitorsPyridazinesAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansMaleNiacinamidePyrazolesasciminibBCR-ABL1 fusion protein, humanFusion Proteins, bcr-ablImidazolesNiacinamideponatinibProtein Kinase InhibitorsPyrazolesPyridazines

Identifiers

PMID39214096
PMCPMC11771825

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.