Evidence map›Paper›PMID 29907599›Full record

ArticleBlood2018

Aggressive B-cell lymphomas in patients with myelofibrosis receiving JAK1/2 inhibitor therapy.

Edit Porpaczy, Sabrina Tripolt, Andrea Hoelbl-Kovacic, Bettina Gisslinger, Zsuzsanna Bago-Horvath, Emilio Casanova-Hevia, Emmanuelle Clappier, Thomas Decker, Sabine Fajmann, Daniela A Fux and 27 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
14.6field-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

70 citing papers in PubMed, 1 synthesis or guideline pooled it, 152 citations in OpenAlex.

  1. JAK inhibitors and COVID-19.Journal for immunotherapy of cancer · 2022
    Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Immunosuppressants/Immunomodulators and Malignancy.Journal of clinical medicine · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Exploring the molecular mechanisms between lymphoma and myelofibrosis.American journal of translational research · 2024
    Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

37 authors at 9 institutions in 3 countries.

Edit PorpaczyDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Sabrina TripoltInstitute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria.
Andrea Hoelbl-KovacicInstitute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria.
Bettina GisslingerDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Zsuzsanna Bago-HorvathInstitute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria.
Emilio Casanova-HeviaLudwig Boltzmann Institute for Cancer Research, Vienna, Austria.
Emmanuelle ClappierINSERM/CNRS UMR 944/7212, Paris, France.
Thomas DeckerMax F. Perutz Laboratories.
Sabine FajmannInstitute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria.
Daniela A FuxInstitute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria.
Georg GreinerDepartment of Laboratory Medicine.
Sinan GueltekinDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Gerwin HellerClinical Division of Oncology, Department of Medicine I, Comprehensive Cancer Center.
Harald HerknerDepartment of Emergency Medicine, and.
Gregor HoermannDepartment of Laboratory Medicine.
Jean-Jacques KiladjianCentre d'Investigations Cliniques, Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis, INSERM, Université Paris 7, Paris, France.
Thomas KolbeBiomodels Austria, University of Veterinary Medicine Vienna, Vienna, Austria.
Christoph KornauthClinical Institute of Pathology, Medical University of Vienna, Vienna, Austria.
Maria-Theresa KrauthDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Robert KralovicsDepartment of Laboratory Medicine.
Leonhard MuellauerClinical Institute of Pathology, Medical University of Vienna, Vienna, Austria.
Mathias MuellerInstitute of Animal Breeding and Genetics, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria; and.
Michaela Prchal-MurphyInstitute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria.
Eva Maria PutzInstitute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria.
Emmanuel RaffouxHematology Department, Hopital Saint Louis, Assistance Publique-Hopitaux de Paris, University Paris Diderot, Paris, France.
Ana-Iris SchieferClinical Institute of Pathology, Medical University of Vienna, Vienna, Austria.
Klaus SchmettererDepartment of Laboratory Medicine.
Christine SchneckenleithnerInstitute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria.
Ingrid Simonitsch-KluppClinical Institute of Pathology, Medical University of Vienna, Vienna, Austria.
Cathrin SkrabsDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Wolfgang R SperrDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Philipp Bernhard StaberDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Birgit StroblInstitute of Animal Breeding and Genetics, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria; and.
Peter ValentDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Ulrich JaegerDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Heinz GisslingerDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Veronika SexlInstitute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, Vienna, Austria.
University of Veterinary Medicine Vienna · ATComprehensive Cancer Center Vienna · ATMedical University of Vienna · ATAssistance Publique – Hôpitaux de Paris · FRLudwig Boltzmann Cluster for Cardiovascular Research · ATCeMM Research Center for Molecular Medicine · ATCentre National de la Recherche Scientifique · FRMax Perutz Labs · ATMunich Leukemia Laboratory (Germany) · DE

Funding

Austrian Science Fund FWF F 2810Austrian Science Fund FWF F 4701Austrian Science Fund FWF F 4704Austrian Science Fund FWF F 4706Austrian Science Fund FWF F 6103Austrian Science Fund FWF F 6106Austrian Science Fund FWF F 6107Austrian Science Fund FWF P 24295Austrian Science Fund FWF P 27132Austrian Science Fund FWF P 27248
6 · The paper itself

Abstract

Inhibition of Janus-kinase 1/2 (JAK1/2) is a mainstay to treat myeloproliferative neoplasms (MPN). Sporadic observations reported the co-incidence of B-cell non-Hodgkin lymphomas during treatment of MPN with JAK1/2 inhibitors. We assessed 626 patients with MPN, including 69 with myelofibrosis receiving JAK1/2 inhibitors for lymphoma development. B-cell lymphomas evolved in 4 (5.8%) of 69 patients receiving JAK1/2 inhibition compared with 2 (0.36%) of 557 with conventional treatment (16-fold increased risk). A similar 15-fold increase was observed in an independent cohort of 929 patients with MPN. Considering primary myelofibrosis only (N = 216), 3 lymphomas were observed in 31 inhibitor-treated patients (9.7%) vs 1 (0.54%) of 185 control patients. Lymphomas were of aggressive B-cell type, extranodal, or leukemic with high MYC expression in the absence of

Indexed as

AnimalsCell Line, TumorFemaleHumansJanus Kinase 1Janus Kinase 2Lymphoma, B-CellMiceMice, KnockoutNeoplasm ProteinsPrimary MyelofibrosisProtein Kinase InhibitorsRetrospective StudiesJAK1 protein, humanJak1 protein, mouseJAK2 protein, humanJak2 protein, mouseJanus Kinase 1Janus Kinase 2Neoplasm ProteinsProtein Kinase Inhibitors

Identifiers

PMID29907599
PMCPMC7115916
OpenAlexW2808491541

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.