Evidence map›Paper›PMID 27966016›Full record

ArticleWiener klinische Wochenschrift2017

Austrian recommendations for the management of primary myelofibrosis, post-polycythemia vera myelofibrosis and post-essential thrombocythemia myelofibrosis: an expert statement.

Thamer Sliwa, Christine Beham-Schmid, Sonja Burgstaller, Veronika Buxhofer-Ausch, Günther Gastl, Klaus Geissler, Maria Krauth, Peter Krippl, Alois Lang, Andreas Petzer and 3 more

Abstract read
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In one paragraph

Article in Wiener klinische Wochenschrift, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Article
  4. Article
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

13 authors at 10 institutions in 1 country.

Thamer Sliwa3rd Medical Department, Hanusch Hospital, Vienna, Austria. thamer.sliwa@wgkk.at.
Christine Beham-SchmidInstitute of Pathology, Medical University of Graz, Graz, Austria.
Sonja BurgstallerDepartment of Internal Medicine IV, Klinikum Wels-Grieskirchen, Wels, Austria.
Veronika Buxhofer-AuschDepartment of Internal Medicine I, Elisabethinen Hospital Linz, Linz, Austria.
Günther GastlDivision of Hematology and Oncology, Innsbruck Medical University, Innsbruck, Austria.
Klaus Geissler5th Medical Department with Hematology, Oncology and Palliative Medicine, Hospital Hietzing, Vienna, Austria.
Maria KrauthDepartment of Internal Medicine I, Division of Hematology and Blood Coagulation, Medical University of Vienna, Vienna, Austria.
Peter KripplDepartment of Internal Medicine with Hematology and Oncology, Steiermärkische Krankenanstaltengesellschaft m. b. H. Krankenhausverbund Feldbach-Fürstenfeld, Fürstenfeld, Austria.
Alois LangDepartment of Internal Medicine, LKH Feldkirch, Feldkirch, Austria.
Andreas PetzerDepartment of Medical Oncology, Hematology and Gastroenterology, Barmherzige Schwestern Hospital Linz, Linz, Austria.
Stefan WöhrerDepartment of Oncology, Landesklinikum Wiener Neustadt, Wiener Neustadt, Austria.
Albert WölflerDivision of Hematology, Medical University of Graz, Graz, Austria.
Heinz GisslingerDepartment of Internal Medicine I, Division of Hematology and Blood Coagulation, Medical University of Vienna, Vienna, Austria.
Medical University of Graz · ATMedical University of Vienna · ATAGO Austria · ATFachhochschule Wiener Neustadt · ATHanusch Hospital · ATInnsbruck Medical University · ATKlinik Hietzing · ATKlinikum Wels-Grieskirchen · ATKrankenhaus der Elisabethinen · ATLandeskrankenhaus Feldkirch · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The entity "myelofibrosis" represents a subgroup of the Philadelphia chromosome-negative myeloproliferative neoplasms. It comprises primary myelofibrosis, post-polycythemia vera myelofibrosis and post-essential thrombocythemia myelofibrosis. This heterogeneous disease is characterized by clonal myeloproliferation, dysregulated kinase signalling and the abnormal expression of several proinflammatory cytokines. Clinically, patients present with symptoms related to thrombocytosis/leukocytosis, anemia and/or progressive splenomegaly. Mutations in Janus kinase 2, an enzyme that is essential for the normal development of erythrocytes, granulocytes, and platelets, notably the V617F mutation, have been identified in approximately 60% of patients with primary myelofibrosis. Recent molecular advances have not only elucidated critical pathways in the pathogenesis of the disease, but also contributed to a more precise assessment of a patient's individual risk. While allogeneic stem cell transplantation remains the only curative treatment, the natural course of the disease and the patient's survival and quality of life may be improved by new treatments, notably ruxolitinib, the first Janus kinase 1/2 inhibitor approved for the management of myelofibrosis. Additional treatment options are being explored.

Indexed as

Expert TestimonyPractice Guidelines as TopicAntibodies, MonoclonalAustriaHematologyMolecular Targeted TherapyPrimary MyelofibrosisAntibodies, MonoclonalJanus kinase inhibitorsManagement recommendationsPost-essential thrombocythemia myelofibrosisPost-polycythemia myelofibrosisPrimary myelofibrosisRuxolitinibTargeted therapies

Identifiers

PMID27966016
OpenAlexW2566767705

What OpenQuestion holds

Textmetadata
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Registered trials

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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.