Evidence map›Paper›PMID 31493432›Full record

ArticleExperimental hematology2019

BCR-ABL1 tyrosine kinase inhibitor K0706 exhibits preclinical activity in Philadelphia chromosome-positive leukemia.

Orlando Antelope, Nadeem A Vellore, Anthony D Pomicter, Ami B Patel, Alexandria Van Scoyk, Phillip M Clair, Michael W Deininger, Thomas O'Hare

Abstract read
In one paragraph

Article in Experimental hematology, 2019. 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. Trial
  2. Review
  3. Article
  4. Current Status of Molecularly Targeted Therapeutics in Blood Cancers.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Review
  7. Review
  8. Parkinson's Disease Modification Through Abl Kinase Inhibition: An Opportunity.Movement disorders : official journal of the Movement Disorder Society · 2022
    Review
  9. Future Directions in Chronic Phase CML Treatment.Current hematologic malignancy reports · 2021
    Review
  10. Review
  11. Review
  12. Potential ApproachesFrontiers in oncology · 2021
    Review
  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

8 authors.

Orlando AntelopeHuntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Nadeem A VelloreHuntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Anthony D PomicterHuntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Ami B PatelHuntsman Cancer Institute, University of Utah, Salt Lake City, UT; Division of Hematology and Hematologic Malignancies, University of Utah, Salt Lake City, UT.
Alexandria Van ScoykHuntsman Cancer Institute, University of Utah, Salt Lake City, UT; Molecular Biology Graduate Program, University of Utah, Salt Lake City, UT.
Phillip M ClairHuntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Michael W DeiningerHuntsman Cancer Institute, University of Utah, Salt Lake City, UT; Division of Hematology and Hematologic Malignancies, University of Utah, Salt Lake City, UT.
Thomas O'HareHuntsman Cancer Institute, University of Utah, Salt Lake City, UT; Division of Hematology and Hematologic Malignancies, University of Utah, Salt Lake City, UT. Electronic address: thomas.ohare@hci.utah.edu.

Funding

Mechanisms of resistance to ponatinib therapy in chronic myeloid leukemiaR01CA178397 · NCI · UNIVERSITY OF UTAH · PI DEININGER, MICHAEL W., O'HARE, THOMAS J. · 2014 to 2018
$2.6M
NCI NIH HHS R01 CA178397
6 · The paper itself

Abstract

BCR-ABL1 tyrosine kinase inhibitors (TKIs) are the cornerstone of treatment in chronic myeloid leukemia. Although there are now four TKIs approved for use in the front-line setting, acquired TKI resistance via secondary kinase domain mutations remains a problem for patients. K0706 is a novel BCR-ABL1 TKI currently under clinical investigation with structural elements similar to those of ponatinib and dasatinib. In this article, we functionally characterize the anti-leukemic activity of K0706 using cell proliferation assays in conjunction with drug resistance screening. We provide details from molecular modeling to support our in vitro findings and additionally describe our limited clinical experience with this drug in two patients treated on trial. We demonstrate that although K0706 retains efficacy against a large spectrum of clinically relevant mutations, it does not appear to have activity against BCR-ABL1

Indexed as

Fusion Proteins, bcr-ablLeukemia, Myelogenous, Chronic, BCR-ABL PositivePhiladelphia ChromosomeAnimalsCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorFemaleHumansMaleMiceProtein Kinase InhibitorsBCR-ABL1 fusion protein, humanFusion Proteins, bcr-ablProtein Kinase Inhibitors

Identifiers

PMID31493432
PMCPMC6803074

What OpenQuestion holds

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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.