Evidence map›Paper›PMID 22772060›Full record

Trial reportLeukemia2013

MK-0457, an Aurora kinase and BCR-ABL inhibitor, is active in patients with BCR-ABL T315I leukemia.

F J Giles, R T Swords, A Nagler, A Hochhaus, O G Ottmann, D A Rizzieri, M Talpaz, J Clark, P Watson, A Xiao and 5 more

Registry-linked trialAbstract readClinical Trial, Phase IClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in Leukemia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00111683 (A Phase I/II Dose Escalation Study of MK0457 in Patients With Leukemia), which is not on this map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.7field-weighted citation impact, top 11% of its field
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.

NCT00111683 phase1completednot on this map

A Phase I/II Dose Escalation Study of MK0457 in Patients With Leukemia

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2005 to 2008Enrolled28ConditionsChronic Myelogenous Leukemia in Blast Crisis, Lymphocytic Leukemia, B Cell, Acute, Myelodysplastic Syndromes, Myelogenous Leukemia, ChronicArmsMK0457
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 65 citations in OpenAlex.

  1. Trial
  2. Advances in Targeting BCR-ABLMolecules (Basel, Switzerland) · 2026
    Review
  3. Article
  4. Article
  5. The two sides of chromosomal instability: drivers and brakes in cancer.Signal transduction and targeted therapy · 2024
    Review
  6. Article
  7. Aurora B Inhibitors as Cancer Therapeutics.Molecules (Basel, Switzerland) · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Recent Advances in Molecular Diagnosis and Prognosis of Childhood B Cell Lineage Acute Lymphoblastic Leukemia (B-ALL).Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2021
    Review
  19. Review
  20. The role of Aurora-A in human cancers and future therapeutics.American journal of cancer research · 2020
    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

15 authors at 11 institutions in 5 countries.

F J GilesHRB Clinical Research Facilities, National University of Ireland Galway and Trinity College Dublin, Galway, Ireland. frankgiles@aol.com
R T Swords
A Nagler
A Hochhaus
O G Ottmann
D A Rizzieri
M Talpaz
J Clark
P Watson
A Xiao
B Zhao
D Bergstrom
P D Le Coutre
S J Freedman
J E Cortes
Merck (Japan) · JPCharité - Universitätsmedizin Berlin · DEDuke University · USGoethe University Frankfurt · DEJena University Hospital · DEMerck & Co., Inc., Rahway, NJ, USA (United States) · USOllscoil na Gaillimhe – University of Galway · IESheba Medical Center · ILThe University of Texas MD Anderson Cancer Center · USUniversity of Miami · USUniversity of Michigan–Ann Arbor · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
6 · The paper itself

Abstract

MK-0457, an Aurora kinase and BCR-ABL inhibitor, was studied on a Phase I/II study in 77 patients with refractory hematologic malignancies. The average number of cycles per patient was 3 (range 1-21). Maximum tolerated doses for a 5-day short infusion and continuous infusion regimens were 40 mg/m(2)/h and 144 mg/m(2)/h, respectively. Drug-related adverse events (AEs) included transient mucositis and alopecia. Eight of 18 patients with BCR-ABL T315I-mutated chronic myelogenous leukemia (44%) had hematologic responses and one of three patients (33%) with Philadelphia chromosome-positive acute lymphoblastic leukemia obtained complete remission. MK-0457 has important activity in patients with leukemias expressing the highly resistant T315I BCR-ABL mutation.

Indexed as

AdolescentAdultAgedAged, 80 and overAurora KinasesCyclopropanesDrug Resistance, NeoplasmFemaleFollow-Up StudiesFusion Proteins, bcr-ablHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLeukemia, Myeloid, AcuteMaleMaximum Tolerated DoseMiddle AgedAurora KinasesCyclopropanesFusion Proteins, bcr-ablPiperazinesProtein Kinase InhibitorsProtein Serine-Threonine KinasesPyrazolesPyrimidinestozasertib

Identifiers

PMID22772060
OpenAlexW1886178005

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.