AI Article Synopsis

  • Triple negative myeloproliferative neoplasms (MPNs) lack classical driver mutations and are not well understood, despite advancements in MPN research.
  • Triple negative primary myelofibrosis (TN-PMF) is associated with a poor prognosis, while triple negative essential thrombocythemia (TN-ET) has a better outlook compared to mutated forms.
  • The review covers clinical features, diagnostics challenges, possible molecular drivers, and current and novel therapies, especially focusing on the difficult-to-treat TN-PMF patients.

Article Abstract

Myeloproliferative neoplasms (MPNs) that lack the classical "driver mutations," termed triple negative MPNs, remain a poorly understood entity. Despite considerable progress toward understanding MPN pathobiology, the mechanisms leading to the development of these MPNs remains inadequately elucidated. While triple negative primary myelofibrosis (TN-PMF) portends a poor prognosis, triple negative essential thrombocythemia (TN-ET) is more favorable as compared with mutated ET. In this review, we summarize the clinical features and prognosis of TN-PMF and -ET as well as diagnostic challenges including identification of non-canonical driver mutations. We also discuss additional molecular drivers to better understand possible pathogenic mechanisms underlying triple negative MPNs. Finally, we highlight current therapeutic approaches as well as novel targets, particularly in the difficult to treat TN-PMF population.

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Source
http://dx.doi.org/10.1080/10428194.2023.2277674DOI Listing

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