The German ONKOPEDIA Guideline for Myelofibrosis in 2025—Recommendations of an MPN Expert Panel of the German Society for Hematology and Oncology (DGHO)
DGHO (Onkopedia) · 2026 · Germany
Source and licence
- Authors
- Martin Griesshammer, Haifa Kathrin Al‐Ali, Gabriela M. Baerlocher et al.
- Title
- The German ONKOPEDIA Guideline for Myelofibrosis in 2025—Recommendations of an MPN Expert Panel of the German Society for Hematology and Oncology (DGHO)
- Journal
- International Journal of Cancer, 2026
- Licence
- CC BY 4.0
- Changes
- Verbatim excerpts; formatting adapted
Full text retrieved 2026-10-27 from Europe PMC · PMC13432566
Licence statement of the original publication
This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
This page reproduces excerpts of the original publication; the original is authoritative. It has not been reviewed by a physician, does not state a recommendation of Medelix and does not replace medical advice. The guideline may have been updated since.
Open the original publication →Full text on Europe PMC
Recommendations
Verbatim, with grade of recommendation or strength of consensus where given.
Recommendations for the Pre‐Fibrotic Phase of Myelofibrosis
- The pre‐fibrotic phase of primary myelofibrosis (pre‐PMF) is now firmly recognized as a distinct clinical and pathological entity within the MPN spectrum, clearly separated from essential thrombocythemia (ET) and overt PMF by the WHO (2016, 2022) and ICC (2022) classifications [7, 8]. The differences between WHO 2022 and ICC 2022 for pre‐PMF are mainly related to wording, emphasis, and the presentation of clonality criteria, whereas the overall diagnostic framework remains highly concordant. Accurate diagnosis is essential but remains challenging, as clinical overlap with ET and early PMF is frequent, and misclassification may lead to inappropriate treatment strategies. Diagnosis requires integration of bone marrow histopathology—characterized by hypercellularity, atypical megakaryopoiesis, and minimal reticulin fibrosis (grade 0–1)—with molecular findings (JAK2, CALR, or MPL mutations, or other clonal markers) and minor criteria including anemia, leukocytosis, splenomegaly, or elevated LDH. Communication between clinicians and expert hematopathologists is strongly recommended to ensure diagnostic precision.
Abstract
The recently published ONKOPEDIA guideline on myelofibrosis, issued under the auspices of the German Society of Hematology and Oncology (DGHO), provides an updated, evidence‐based framework for the diagnosis and management of this rare, chronic myeloproliferative neoplasm. Developed by a panel of experts (including Germany, Austria and Switzerland) nominated by the DGHO, the guideline reflects a structured and consensus‐oriented process in which internationally recognized specialists in hematology critically reviewed the available evidence, revised the written draft, and engaged in multiple rounds of discussion to ensure consistency, clinical relevance, and scientific rigor. This update builds upon the foundation of the previously available ONKOPEDIA guideline (accessible at www.onkopedia.com), but extends and refines the recommendations in light of several important recent developments.
Contents of the original publication
The section headings of the original.
- Guideline Generation by an International Expert Panel
- The 2025 Update of the ONKOPEDIA Guidelines on MF
- Stronger Emphasis on Symptom Burden
- Recommendations for the Pre‐Fibrotic Phase of Myelofibrosis
- Use of Molecular Risk Scores
- Update on JAK‐Inhibitor Use and Stratification
- New Therapeutic Options
- Identification of Ruxolitinib Failure by Clinical Practice Tools
- The Updated MF‐ONKOPEDIA‐Guidelines in Context of International Treatment Recommendations: Comparison With the NCCN‐Guidelines for MF
- Risk Stratification and Diagnostic Frameworks
- Weighting of Symptom Burden in Initial Assessment and Follow‐Up
- JAK‐Inhibitor Selection and Sequencing: Platelets, Anemia, and Geography
- Management of MF‐Associated Anemia and “New” Options
- Recognition of Ruxolitinib Failure and Timing of Transition
- Transplant Referral and Timing Strategies
- Novel Therapeutic Approaches and Pipeline Integration
- Summary
- Key Messages
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