How I manage myeloproliferative neoplasm-unclassifiable: Practical approaches for 2022 and beyond
Donal P McLornan1,2, Rupen Hargreaves2, Juan Carlos Hernández-Boluda3
1Department of Haematology, 4th Floor Southwark Wing, Guy's and St. Thomas' NHS Foundation Trust, Great Maze Pond, London, UK.
Abstract:
Myeloproliferative neoplasm (MPN)-unclassifiable (MPN-U) or not otherwise specified represents a rare, poorly defined and heterogeneous group of MPNs. Disease incidence is difficult to define but likely represents close to 5% of all MPNs when strict World Health Organisation (WHO) criteria are applied. Dynamic review over time is required to assess if the disease can be re-classified into another MPN entity. A diagnosis of MPN-U leads to many challenges for both the patient and physician alike including lack of agreed monitoring and therapeutic guidelines, validated prognostic markers and licenced therapies coupled with exclusion from clinical trials. MPN-U has an inherent risk of an aggressive clinical course and transformation in some but who, and when to treat in the chronic phase, including identifying who may require more aggressive therapy at an earlier stage, remains elusive. Moreover, despite the significant thrombotic risk, there is no agreement on systematic primary thromboprophylaxis. We hereby provide a contemporary overview of MPN-U in addition to four illustrative cases providing our collective suggested approaches to clinical challenges.
Insights
Myeloproliferative neoplasm-unclassifiable (MPN-U) is a rare MPN group lacking clear guidelines. This overview addresses diagnostic and therapeutic challenges for MPN-U patients.
Area of Science:
- Hematology
- Oncology
Background:
- Myeloproliferative neoplasm-unclassifiable (MPN-U) is a rare, heterogeneous hematologic disorder.
- MPN-U diagnosis presents challenges due to lack of defined monitoring, therapeutic guidelines, prognostic markers, and licensed therapies.
Purpose of the Study:
- To provide a contemporary overview of MPN-U.
- To suggest approaches for clinical challenges associated with MPN-U.
Main Methods:
- Literature review and analysis of current understanding of MPN-U.
- Presentation of four illustrative cases to demonstrate clinical management strategies.
Main Results:
- MPN-U constitutes approximately 5% of MPNs under strict WHO criteria.
- The condition carries an inherent risk of aggressive clinical course and transformation.
- There is a significant thrombotic risk without agreed-upon thromboprophylaxis guidelines.
Conclusions:
- MPN-U requires dynamic review for potential reclassification into other MPN entities.
- Addressing the diagnostic, prognostic, and therapeutic uncertainties in MPN-U is crucial for patient care.
- Further research and guideline development are needed for optimal management of MPN-U.
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