Evidence map›Paper›PMID 24687085›Full record

ArticleBlood2014

Patients with myeloid malignancies bearing PDGFRB fusion genes achieve durable long-term remissions with imatinib.

Chan Y Cheah, Kate Burbury, Jane F Apperley, Francoise Huguet, Vincenzo Pitini, Martine Gardembas, David M Ross, Donna Forrest, Philippe Genet, Philippe Rousselot and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 2 pooled it
11.0field-weighted citation impact, top 1% 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

57 citing papers in PubMed, 2 syntheses or guidelines pooled it, 137 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Trial
  4. Review
  5. Review
  6. Article
  7. Case reports in hematology · 2026
    Article
  8. Article
  9. Article
  10. Tumour-agnostic kinase inhibitors.Nature reviews. Drug discovery · 2025
    Review
  11. Review
  12. Resistance to imatinib in aFrontiers in oncology · 2025
    Article
  13. Case reports in hematology · 2025
    Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Myeloid/Lymphoid Neoplasms withJournal of inflammation research · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 17 institutions in 7 countries.

Chan Y CheahDepartment of Haematology, Peter MacCallum Cancer Centre, East Melbourne, VIC, Australia; University of Melbourne, Parkville, VIC, Australia;
Kate BurburyDepartment of Haematology, Peter MacCallum Cancer Centre, East Melbourne, VIC, Australia; University of Melbourne, Parkville, VIC, Australia;
Jane F ApperleyDepartment of Haematology, Faculty of Medicine, Imperial College London, London, United Kingdom;
Francoise HuguetDepartment of Haematology, Centre Hospitalier Universitaire, Toulouse, France;
Vincenzo PitiniOncologia Medica e Trapianto di Midollo Osseo, Messina, Italy;
Martine GardembasDepartment of Haematology, Centre Hospitalier Universitaire, Angers, France;
David M RossHaematology, South Australia Pathology, Adelaide, SA, Australia; School of Medicine, University of Adelaide, Adelaide, SA, Australia; School of Medicine, Flinders University, Adelaide, SA, Australia;
Donna ForrestBritish Columbia Cancer Agency, Vancouver, BC, Canada;
Philippe GenetDepartment of Haematology, Hôpital Victor Dupouy, Argenteuil, France;
Philippe RousselotDepartment of Haematology, Hôpital de Versailles and Université de Versailles Saint-Quentin, Le Chesnay, France;
Nigel PattonDepartment of Haematology, Auckland City Hospital, Auckland, New Zealand;
Graeme SmithDepartment of Haematology, St. James's University Hospital, Leeds, United Kingdom;
Cynthia E DunbarHematology Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD;
Sawa ItoHematology Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD;
Ricardo C T AguiarDepartment of Medicine, University of Texas Health Science Center, San Antonio, TX; Audie Murphy Veterans Affairs Hospital, San Antonio, TX;
Olatoyosi OdenikeDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL;
Alla GimelfarbNorthshore University Health Systems, Chicago, IL;
Nicholas C P CrossFaculty of Medicine, University of Southampton, Southampton, United Kingdom.
John F SeymourDepartment of Haematology, Peter MacCallum Cancer Centre, East Melbourne, VIC, Australia; University of Melbourne, Parkville, VIC, Australia;
The University of Melbourne · AUAuckland City Hospital · NZBC Cancer Agency · CACentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Toulouse · FRCentre Hospitalier Victor Dupouy · FRImperial College London · GBMurphy Oil Corporation (United States) · USNational Heart Lung and Blood Institute · USNational Institutes of Health · USNorthShore University HealthSystem · USOspedale Sant'Anna · ITPeter MacCallum Cancer Centre · AUSt James's University Hospital · GBThe University of Adelaide · AUUniversity of Chicago · USUniversity of Southampton · GB

Funding

Novel therapies for bone marrow failure and Diamond-Blackfan AnemiaZIAHL006186 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DUNBAR, CYNTHIA E · 2014 to 2025
$5.7M
6 · The paper itself

Abstract

Myeloid neoplasms and eosinophilia with rearrangements of PDGFRB are uncommon Philadelphia-negative myeloproliferative neoplasms. Patients are typically male, with morphologic features of a Philadelphia-negative chronic myeloproliferative syndrome or chronic myelomonocytic leukemia with eosinophilia. Reciprocal translocations involving PDGFRB result in fusion genes with constitutively activated receptor tyrosine kinase sensitive to inhibition with imatinib. We present an updated and expanded analysis of a cohort of 26 such patients treated with imatinib. After a median follow-up of 10.2 years (range, 1.8-17 years), the 10-year overall survival rate was 90% (95% confidence interval, 64%-97%); after median imatinib duration of 6.6 years (range, 0.1-12 years), the 6-year progression-free survival rate was 88% (95% confidence interval, 65%-96%). Of the patients, 96% responded; no patients who achieved a complete cytogenetic (n = 13) or molecular (n = 8) remission lost their response or progressed to blast crisis. Imatinib is well-tolerated and achieves excellent long-term responses in patients with PDGFRB rearrangements.

Indexed as

AdolescentAdultAgedAntineoplastic AgentsBenzamidesChildChild, PreschoolEosinophiliaFemaleHumansImatinib MesylateInfantLeukemia, MyeloidMaleMiddle AgedOncogene Proteins, FusionAntineoplastic AgentsBenzamidesImatinib MesylateOncogene Proteins, FusionPiperazinesPyrimidinesReceptor, Platelet-Derived Growth Factor beta

Identifiers

PMID24687085
PMCPMC4047496
OpenAlexW2130669032

What OpenQuestion holds

Textmetadata
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.