Evidence map›Paper›PMID 20017607›Full record

ReviewLeukemia & lymphoma2009

Advances in treatment of chronic myelogenous leukemia--new treatment options with tyrosine kinase inhibitors.

Fabio P S Santos, Farhad Ravandi

Open access · greenAbstract readEvaluation StudyReview
In one paragraph

Review in Leukemia & lymphoma, 2009. 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
1.8field-weighted citation impact, top 14% 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.

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, 27 citations in OpenAlex.

  1. The silent players: AtypicalOncology reports · 2025
    Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. An adaptive Src-PDGFRA-Raf axis in rhabdomyosarcoma.Biochemical and biophysical research communications · 2012
    Article
  9. Article
  10. Article
  11. Disruption of Bcr-Abl coiled coil oligomerization by design.The Journal of biological chemistry · 2011
    Article
  12. Article
  13. Article
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

2 authors at 1 institution in 1 country.

Fabio P S SantosDepartment of Leukemia, University of Texas - M. D. Anderson Cancer Center, Houston, TX 77030, USA.
Farhad Ravandi
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Imatinib is considered standard therapy for patients with chronic myelogenous leukemia (CML), inducing a high rate of hematologic and cytogenetic responses. Despite these excellent results, several patients develop resistance to imatinib. Mechanisms of resistance are varied and include BCR-ABL1 kinase domain mutations, decreased entry of imatinib into cells, acquisition of secondary genetic changes and activation of alternate signaling pathways. Second-generation tyrosine kinase inhibitors (TKI) (dasatinib, nilotinib) were developed as an alternative for patients that develop resistance or are intolerant to imatinib. Dasatinib is a dual Abl/Src kinase TKI that is structurally unrelated to imatinib and is approved for therapy of all phases of CML in patients who are resistant or intolerant to imatinib. Nilotinib is a compound related to imatinib that has greater specificity and improved binding characteristics, and has clinical activity in the setting of imatinib failure. Resistance to multiple TKIs does occur, particularly in patients with the T315I mutation. Several new agents are in development including new TKIs, aurora kinase inhibitors and homoharringtonine.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBenzamidesClinical Trials as TopicDasatinibDrug Resistance, NeoplasmHumansImatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveModels, BiologicalPiperazinesProtein Kinase InhibitorsProtein-Tyrosine KinasesPyrimidinesThiazolesBenzamidesDasatinibImatinib MesylatenilotinibPiperazinesProtein Kinase InhibitorsProtein-Tyrosine KinasesPyrimidinesThiazoles

Identifiers

PMID20017607
PMCPMC4109296
OpenAlexW2096554832

What OpenQuestion 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 OpenQuestion graph.