Evidence map›Paper›PMID 26371371›Full record

ReviewBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2015

Hematopoietic Cell Transplantation as Curative Therapy for Patients with Myelofibrosis: Long-Term Success in all Age Groups.

H Joachim Deeg, Christopher Bredeson, Stephanie Farnia, Karen Ballen, Vikas Gupta, Ruben A Mesa, Uday Popat, Parameswaran Hari, Wael Saber, Matthew Seftel and 2 more

Open access · hybridAbstract readReview
In one paragraph

Review in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Myeloproliferative Neoplasms, Version 2.2017, NCCN Clinical Practice Guidelines in Oncology.Journal of the National Comprehensive Cancer Network : JNCCN · 2016
    Guideline
  2. Assessment of Quality of Life following Allogeneic Stem Cell Transplant for Myelofibrosis.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
  3. Patient Perspectives Regarding Allogeneic Bone Marrow Transplantation in Myelofibrosis.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
  4. Article
  5. Article
  6. Article
  7. Novel treatments for myelofibrosis: beyond JAK inhibitors.International journal of hematology · 2022
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Observational
  15. Review
  16. Article
  17. Article
  18. Article
  19. Myelofibrosis: to transplant or not to transplant?Hematology. American Society of Hematology. Education Program · 2016
    Review
  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

12 authors at 11 institutions in 2 countries.

H Joachim DeegFred Hutchinson Cancer Research Center and the University of Washington School of Medicine, Seattle, Washington. Electronic address: jdeeg@fredhutch.org.
Christopher BredesonOttawa Hospital Research Institute at University of Ottawa, Ottawa, Canada.
Stephanie FarniaNational Marrow Donor Program, Minneapolis, Minnesota.
Karen BallenHematology/Oncology Division, Massachusetts General Hospital, Boston, Massachusetts.
Vikas GuptaMedical Oncology and Hematology, Princess Margaret Cancer Center, University of Toronto, Toronto, Canada.
Ruben A MesaDivision of Hematology and Medical Oncology, Mayo Clinic Cancer Center, Scottsdale, Arizona.
Uday PopatDepartment of Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, Texas.
Parameswaran HariDivision of Hematology/Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Wael SaberDivision of Hematology/Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Matthew SeftelSection of Hematology/Oncology, University of Manitoba, Winnipeg, Canada.
Roni TamariAdult Bone Marrow Transplantation Service, Memorial Sloan Kettering Cancer Center, New York, New York; Department of Medicine, Weill Cornell Medical College, New York, New York.
Effie W PetersdorfFred Hutchinson Cancer Research Center and the University of Washington School of Medicine, Seattle, Washington.
Medical College of Wisconsin · USCornell University · USFred Hutch Cancer Center · USMassachusetts General Hospital · USMayo Clinic in Arizona · USNational Marrow Donor Program · USThe University of Texas MD Anderson Cancer Center · USUniversity of Manitoba · CAUniversity of Ottawa · CAUniversity of Toronto · CAUniversity of Washington · US

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
NOVEL THERAPEUTIC STRATEGIES IN MYELODYSPLASTIC SYNDROMER01CA087948 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DEEG, H. JOACHIM · 2000 to 2003
$1.6M
NCI NIH HHS R01 CA087948NCI NIH HHS U24 CA076518
6 · The paper itself

Abstract

Myeloproliferative neoplasms (MPN) are chronic marrow disorders with variable prognoses. Most patients with polycythemia vera, essential thrombocythemia, or even primary myelofibrosis (PMF) are successfully treated with conservative strategies for years or even decades, and recent data suggest that even in patients with high-risk disease, in particular those with PMF, life expectancy can be extended by treatment with janus kinase (JAK2) inhibitors. However, none of those modalities are curative, and after marrow failure develops, the disease "accelerates," or transforms to acute leukemia, the only option able to effectively treat and, in fact, cure MPN is allogeneic hematopoietic cell transplantation (HCT). Outcome is superior if HCT is performed before leukemic transformation occurs. Several reports document survival in unmaintained remission beyond 10 years. The most recent analyses show reduced regimen-related mortality (less than 10% or even 5% at day 100) and progressively improved survival with both HLA-identical sibling and unrelated donors. The development of low/reduced-intensity conditioning regimens has contributed to the improved success rate and has allowed successful HCT in patients in their seventh and even eighth decade of life. We propose, therefore, that HCT should be offered to fit patients in these age groups and should be covered by their respective insurance carriers.

Indexed as

Hematopoietic Stem Cell TransplantationAcute DiseaseAdultAgedDisease ProgressionHumansLeukemiaMiddle AgedMyeloablative AgonistsPrimary MyelofibrosisSiblingsSurvival AnalysisTransplantation ConditioningTransplantation, HomologousUnrelated DonorsMyeloablative AgonistsEssential thrombocythemiaHematopoietic cell transplantationMyeloproliferative neoplasmsPolycythemia veraPrimary myelofibrosis

Identifiers

PMID26371371
PMCPMC4604067
OpenAlexW1766283728

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.