Evidence map›Paper›PMID 26493563›Full record

Trial reportBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2016

Outcomes of Allogeneic Hematopoietic Cell Transplantation in Patients with Myelofibrosis with Prior Exposure to Janus Kinase 1/2 Inhibitors.

Mohamed Shanavas, Uday Popat, Laura C Michaelis, Veena Fauble, Donal McLornan, Rebecca Klisovic, John Mascarenhas, Roni Tamari, Murat O Arcasoy, James Davies and 15 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 3 pooled it
7.6field-weighted citation impact, top 2% 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

61 citing papers in PubMed, 3 syntheses or guidelines pooled it, 142 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Myeloproliferative Neoplasms, Version 2.2017, NCCN Clinical Practice Guidelines in Oncology.Journal of the National Comprehensive Cancer Network : JNCCN · 2016
    Guideline
  4. Trial
  5. Trial
  6. Ruxolitinib Therapy Followed by Reduced-Intensity Conditioning for Hematopoietic Cell Transplantation for Myelofibrosis: Myeloproliferative Disorders Research Consortium 114 Study.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
  7. Trial
  8. Trial
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Observational
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review

1 more citing papers are in PubMed but not listed here.

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

25 authors at 16 institutions in 3 countries.

Mohamed ShanavasMPN Program, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Uday PopatDepartment of Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, Texas.
Laura C MichaelisDepartment of Medicine, Division of Hematology/Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Veena FaubleDepartment of Hematology and Oncology, Mayo Clinic Cancer Center, Scottsdale, Arizona.
Donal McLornanDepartment of Haematological Medicine, King's College Hospital NHS Foundation Trust, London, United Kingdom.
Rebecca KlisovicDepartment of Internal Medicine, Ohio State University Wexner Medical Center, Columbus, Ohio.
John MascarenhasTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Roni TamariDepartment of Medicine, Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Murat O ArcasoyDivision of Cellular Therapy and Hematologic Malignancies, Duke Cancer Institute, Duke University School of Medicine, Durham, North Carolina.
James DaviesOxford University Hospitals NHS trust, Oxford, UK.
Usama GergisDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Oluchi C UkaegbuDepartment of Internal Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Rammurti T KambleCenter for Cell and Gene Therapy, Baylor College of Medicine and Houston Methodist Hospital, Houston, Texas.
John M StorringDepartment of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.
Navneet S MajhailBlood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.
Rizwan RomeeDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
Srdan VerstovsekHanns A. Pielenz Clinical Research Center for Myeloproliferative Neoplasms, Department of Leukemia, MD Anderson Cancer Center, Houston, TX, US.
Antonio PagliucaDepartment of Haematological Medicine, King's College Hospital NHS Foundation Trust, London, United Kingdom.
Sumithira VasuDepartment of Internal Medicine, Ohio State University Wexner Medical Center, Columbus, Ohio.
Brenda ErnstDepartment of Hematology and Oncology, Mayo Clinic Cancer Center, Scottsdale, Arizona.
Eshetu G AtenafuDepartment of Biostatistics, Princess Margaret Cancer Centre, Toronto, ON, Canada.
Ahmad HanifDepartment of Medicine, Division of Hematology/Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Richard ChamplinDepartment of Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, Texas.
Paremeswaran HariDepartment of Medicine, Division of Hematology/Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Vikas GuptaMPN Program, Princess Margaret Cancer Centre, Toronto, Ontario, Canada. Electronic address: vikas.gupta@uhn.ca.
Medical College of Wisconsin · USPrincess Margaret Cancer Centre · CAThe University of Texas MD Anderson Cancer Center · USKing's College Hospital NHS Foundation Trust · GBMayo Clinic in Arizona · USThe Ohio State University Wexner Medical Center · USCleveland Clinic · USCornell University · USDuke University · USIcahn School of Medicine at Mount Sinai · USMcGill University Health Centre · CAMemorial Sloan Kettering Cancer Center · USMethodist Hospital · USOxford University Hospitals NHS Trust · GBVanderbilt University Medical Center · USWashington University in St. Louis · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Tissue BankP01CA108671 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Ronald Hoffman · 2006 to 2026
$82.0M
NCI NIH HHS P01 CA108671NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

The impact of Janus kinase (JAK) 1/2 inhibitor therapy before allogeneic hematopoietic cell transplantation (HCT) has not been studied in a large cohort in myelofibrosis (MF). In this retrospective multicenter study, we analyzed outcomes of patients who underwent HCT for MF with prior exposure to JAK1/2 inhibitors. One hundred consecutive patients from participating centers were analyzed, and based on clinical status and response to JAK1/2 inhibitors at the time of HCT, patients were stratified into 5 groups: (1) clinical improvement (n = 23), (2) stable disease (n = 31), (3) new cytopenia/increasing blasts/intolerance (n = 15), (4) progressive disease: splenomegaly (n = 18), and (5) progressive disease: leukemic transformation (LT) (n = 13). Overall survival (OS) at 2 years was 61% (95% confidence interval [CI], 49% to 71%). OS was 91% (95% CI, 69% to 98%) for those who experienced clinical improvement and 32% (95% CI, 8% to 59%) for those who developed LT on JAK1/2 inhibitors. In multivariable analysis, response to JAK1/2 inhibitors (P = .03), dynamic international prognostic scoring system score (P = .003), and donor type (P = .006) were independent predictors of survival. Among the 66 patients who remained on JAK1/2 inhibitors until stopped for HCT, 2 patients developed serious adverse events necessitating delay of HCT and another 8 patients had symptoms with lesser severity. Adverse events were more common in patients who started tapering or abruptly stopped their regular dose ≥6 days before conditioning therapy. We conclude that prior exposure to JAK1/2 inhibitors did not adversely affect post-transplantation outcomes. Our data suggest that JAK1/2 inhibitors should be continued near to the start of conditioning therapy. The favorable outcomes of patients who experienced clinical improvement with JAK1/2 inhibitor therapy before HCT were particularly encouraging, and need further prospective validation.

Indexed as

Hematopoietic Stem Cell TransplantationPrimary MyelofibrosisProtein Kinase InhibitorsAdultAgedAllograftsDisease-Free SurvivalFemaleHumansJanus Kinase 1Janus Kinase 2Middle AgedRetrospective StudiesSurvival RateJAK1 protein, humanJAK2 protein, humanJanus Kinase 1Janus Kinase 2Protein Kinase InhibitorsAllogeneic transplantationJAK1/2 inhibitorsMyelofibrosisRuxolitinibSurvival

Identifiers

PMID26493563
PMCPMC5030817
OpenAlexW2176736150

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.