Evidence map›Paper›PMID 39888352›Full record

ArticleAnnals of hematology2025

How I diagnose and treat patients in the pre-fibrotic phase of primary myelofibrosis (pre-PMF) - practical approaches of a German expert panel discussion in 2024.

Martin Griesshammer, Haifa Kathrin Al-Ali, Jan-Niklas Eckardt, Michael Fiegl, Joachim Göthert, Kathleen Jentsch-Ullrich, Steffen Koschmieder, Hans Michael Kvasnicka, Andreas Reiter, Burkhard Schmidt and 1 more

Abstract read
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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.

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

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

  1. Guideline
  2. Review
  3. Article
  4. [Myelofibrosis: watch and wait or treat?]Innere Medizin (Heidelberg, Germany) · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Myelofibrosis: Treatment Options After Ruxolitinib Failure.Current oncology (Toronto, Ont.) · 2025
    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

11 authors.

Martin GriesshammerOncology, Haemostaseology and Palliative Care, Johannes Wesling Medical Center Minden, University Clinic for Hematology, University of Bochum, Bochum, Germany.
Haifa Kathrin Al-AliKrukenberg Cancer Center, University Hospital of Halle, Halle, Germany.
Jan-Niklas EckardtDepartment of Internal Medicine I, University Hospital Dresden, Dresden, Germany.
Michael FieglHämatologie Onkologie Germering, Germering, Germany.
Joachim GöthertDepartment of Hematology and Stem Cell Transplantation, University Hospital Essen, Essen, Germany.
Kathleen Jentsch-UllrichGemeinschaftspraxis Hämatologie und Onkologie, Magdeburg, Germany.
Steffen KoschmiederDepartment of Hematology, Oncology, Hemostaseology, and Stem Cell Transplantation, Faculty of Medicine, RWTH Aachen University, Aachen, Germany.
Hans Michael KvasnickaFakultät für Gesundheit (Department für Humanmedizin), Pathologie, Universität Witten/Herdecke, Herdecke, Germany.
Andreas ReiterDepartment of Hematology and Oncology, University Hospital Mannheim, Mannheim, Germany.
Burkhard SchmidtHämatologie und Onkologie München Pasing MVZ GmbH, München, Germany.
Florian H HeidelHematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School (MHH), Hannover, Germany. heidel.florian@mh-hannover.de.ORCID http://orcid.org/0000-0003-2438-1955

Funding

Deutsche Forschungsgemeinschaft 428858786Deutsche Forschungsgemeinschaft 517204983
6 · The paper itself

Abstract

The prefibrotic phase of primary myelofibrosis (pre-PMF) represents a distinct subentity within the spectrum of myeloproliferative neoplasms (MPNs), recognized by the World Health Organization (WHO) and the International Consensus Classification (ICC). Pre-PMF is characterized by unique morphological, clinical, and molecular features, distinguishing it from essential thrombocythemia (ET) and overt myelofibrosis (overt-PMF). The diagnostic process for pre-PMF relies on bone marrow histology, identification of molecular mutations and exclusion of other myeloid neoplasms. Misclassification remains a significant challenge due to overlapping phenotypes and the heterogeneity of clinical presentations, which range from asymptomatic cases to severe cytopenias and a high thrombotic risk. Management strategies for pre-PMF focus on mitigating symptom burden, reducing thromboembolic events, and preventing disease progression. Low-risk patients often benefit from observational approaches or low-dose aspirin, while cytoreductive therapies, such as hydroxyurea or interferon-alpha, are utilized in symptomatic or high-risk cases. JAK inhibitors like ruxolitinib have shown promise in addressing splenomegaly and systemic symptoms, although their role in pre-PMF requires further investigation. Advances in artificial intelligence are enhancing diagnostic precision by refining bone marrow histopathological analysis, paving the way for more accurate disease classification and tailored therapeutic strategies. This position paper integrates insights from a German expert panel discussion, underscoring the need for interdisciplinary collaboration, adherence to updated WHO/ICC diagnostic criteria, and personalized treatment approaches. By addressing diagnostic challenges and therapeutic nuances, it seeks to improve outcomes and quality of life for patients navigating the complexities of pre-PMF.

Indexed as

Primary MyelofibrosisGermanyHumansPractice Guidelines as TopicPyrazolesThrombocythemia, EssentialPyrazolesMPNMyeloproliferative neoplasmPrefibrotic myelofibrosisPre-PMFTargeted therapy

Identifiers

PMID39888352
PMCPMC11868337

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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.