All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a healthcare professional. If you are a patient or carer, please visit the MPN Advocates Network.
The MPN Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the MPN Hub cannot guarantee the accuracy of translated content. The MPN Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The MPN Hub is an independent medical education platform, sponsored by GSK, Novartis, AOP, Sobi and Takeda and supported through independent educational grants from Bristol Myers Squibb, Blueprint Medicines, Incyte and Merck Sharp & Dohme LLC, Rahway, NJ, USA. Funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders.
Now you can support HCPs in making informed decisions for their patients
Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.
Find out more
Create an account to access:
Bookmark & personalize site content
Receive alerts for new content in your areas of interest
View MPN content recommended for you
Updates from the National Comprehensive Cancer Network (NCCN) Guidelines for Myeloproliferative Neoplasms (MPN), Version 2.2026, were published in the Journal of the National Comprehensive Cancer Network by Gerds et al. These guideline insights focus on updates for the treatment of myelofibrosis (MF).
Key data: Key updates include revised risk stratification models for post-polycythemia vera (PV) and post-essential thrombocythemia (ET) MF, with the Mutation and Karyotype-Enhanced International Prognostic Scoring System Version 2.0 for patients aged ≤70 years (MIPSS70+ v2.0) designated as the preferred prognostic model. Momelotinib and pacritinib were added as Janus kinase inhibitor (JAKi) treatment options across risk categories. Updated anemia management pathways now position momelotinib as a Category 1 preferred option for patients with ongoing symptomatic splenomegaly and/or constitutional symptoms, while clinical trial enrollment is a preferred option across the anemia management scenarios. Post-allogeneic hematopoietic stem cell transplantation (allo-HSCT) measurable residual disease (MRD) monitoring is also now recommended.
Key learning: Version 2.2026 of the NCCN Guidelines for MPN introduces clinically meaningful updates for MF, including expanded JAKi treatment options, refined anemia management algorithms that prioritize momelotinib in appropriate patients, and updated guidance on MRD monitoring after allo-HSCT.
References
Please indicate your level of agreement with the following statements:
The content was clear and easy to understand
The content addressed the learning objectives
The content was relevant to my practice
I will change my clinical practice as a result of this content
Your opinion matters
Do you include basal serum tryptase (bST) testing in the diagnostic evaluation of patients with MPN?