Evidence map›Paper›PMID 26341525›Full record

ArticleHaematologica2015

An International MDS/MPN Working Group's perspective and recommendations on molecular pathogenesis, diagnosis and clinical characterization of myelodysplastic/myeloproliferative neoplasms.

Tariq I Mughal, Nicholas C P Cross, Eric Padron, Ramon V Tiu, Michael Savona, Luca Malcovati, Raoul Tibes, Rami S Komrokji, Jean-Jacques Kiladjian, Guillermo Garcia-Manero and 8 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Haematologica, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06414681 (An Open Label Pilot Trial of the Combination of Tagraxofusp With Pacritinib in Patients With Intermediate-1 or Higher Myelofibrosis, Who Have Had Prior Therapy With the Approved JAK Inhibitors or in Which Therapy With the Approved JAK Inhibitors is Not Appropriate, Contraindicated or Declined), which is not on this map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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.

NCT06414681 early_phase1recruitingnot on this mapstarted 2025, after this paper: background citation

An Open Label Pilot Trial of the Combination of Tagraxofusp With Pacritinib in Patients With Intermediate-1 or Higher Myelofibrosis, Who Have Had Prior Therapy With the Approved JAK Inhibitors or in Which Therapy With the Approved JAK Inhibitors is Not Appropriate, Contraindicated or Declined

TypeinterventionalSponsorUniversity of Kansas Medical CenterRan2025 to 2026Enrolled20ConditionsMyelofibrosis,MFArmsTagraxofusp, Pacritinib
3 · Its place in the literature

Who cites it

39 citing papers in PubMed.

  1. Trial
  2. Molecular-Based Ecosystem to Improve Personalized Medicine in Chronic Myelomonocytic Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  3. Myeloproliferative Neoplasms: Contemporary Review and Molecular Landscape.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Molecular Pathogenesis ofFrontiers in oncology · 2021
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

18 authors.

Tariq I MughalTufts University Medical Center, Boston, MA, USA tmughal911@hotmail.com.
Nicholas C P CrossWessex Regional Genetics Laboratory, Salisbury, UK.
Eric PadronH. Lee Moffitt Cancer Center, Tampa, FL, USA.
Ramon V TiuCleveland Clinic Taussig Cancer Institute, OH, USA.
Michael SavonaVanderbilt University Medical Center, Nashville, TN, USA.
Luca MalcovatiUniversity of Pavia Medical School, S. Matteo University Hospital, Pavia, Italy.
Raoul TibesMayo Clinic Cancer Center, Scottsdale, AZ, USA.
Rami S KomrokjiH. Lee Moffitt Cancer Center, Tampa, FL, USA.
Jean-Jacques KiladjianHôpital Saint-Louis, Paris 7, France.
Guillermo Garcia-ManeroMD Anderson Cancer Center, Houston, TX, USA.
Attilio OraziWeill Cornell Medical College, New York, NY, USA.
Ruben MesaMayo Clinic Cancer Center, Scottsdale, AZ, USA.
Jaroslaw P MaciejewskiCleveland Clinic Taussig Cancer Institute, OH, USA.
Pierre FenauxHôpital Saint-Louis, Paris 7, France.
Raphael ItzyksonHôpital Saint-Louis, Paris 7, France.
Ghulam MuftiKing's College Hospital, GKT School of Medicine, London, UK.
Eric SolaryInstitut Gustave Roussy, Villejuif, France.
Alan F ListH. Lee Moffitt Cancer Center, Tampa, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the 2008 WHO classification, chronic myeloid malignancies that share both myelodysplastic and myeloproliferative features define the myelodysplastic/myeloproliferative group, which includes chronic myelomonocytic leukemia, juvenile myelomonocytic leukemia, atypical chronic myeloid leukemia, refractory anemia with ring sideroblasts and thrombocytosis, and myelodysplastic/myeloproliferative unclassified. With the notable exception of refractory anemia with ring sideroblasts and thrombocytosis, there is much overlap among the various subtypes at the molecular and clinical levels, and a better definition of these entities, an understanding of their biology and an identification of subtype-specific molecular or cellular markers are needed. To address some of these challenges, a panel comprised of laboratory and clinical experts in myelodysplastic/myeloproliferative was established, and four independent academic MDS/MPN workshops were held on: 9(th) March 2013, in Miami, Florida, USA; 6(th) December 2013, in New Orleans, Louisiana, USA; 13(th) June 2014 in Milan, Italy; and 5(th) December 2014 in San Francisco, USA. During these meetings, the current understanding of these malignancies and matters of biology, diagnosis and management were discussed. This perspective and the recommendations on molecular pathogenesis, diagnosis and clinical characterization for adult onset myelodysplastic/myeloproliferative is the result of a collaborative project endorsed and supported by the MDS Foundation.

Indexed as

Hematologic NeoplasmsMyelodysplastic-Myeloproliferative DiseasesAdultFemaleHumansMalePractice Guidelines as Topic

Identifiers

PMID26341525
PMCPMC4800699

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