Understanding triple negative myeloproliferative neoplasms: pathogenesis, clinical features, and management

Research output: Contribution to journalReview articlepeer-review

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 JAK2 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.

Original languageEnglish
Pages (from-to)158-167
Number of pages10
JournalLeukemia and Lymphoma
Volume65
Issue number2
DOIs
StatePublished - 2024

Keywords

  • JAK2
  • KRAS
  • Myelofibrosis
  • essential thrombocythemia
  • triple negative

Fingerprint

Dive into the research topics of 'Understanding triple negative myeloproliferative neoplasms: pathogenesis, clinical features, and management'. Together they form a unique fingerprint.

Cite this