Literature DB >> 26825696

New molecular genetics in the diagnosis and treatment of myeloproliferative neoplasms.

Francesco Passamonti1, Barbara Mora, Margherita Maffioli.   

Abstract

PURPOSE OF REVIEW: Myeloproliferative neoplasms (MPN) are conditions of great interest because of the identification of their molecular basis and of the entering of new small molecules into clinical practice. The aim of this review is to report the role of mutations in the diagnosis, prognosis, and in the prediction of response to JAK inhibitors in MPN. RECENT
FINDINGS: New mutations of the CALR gene have been discovered in patients without JAK2 or MPL mutations and are now included in the World Health Organization classification system. The role of ASXL1 and SRSF2 together with the driver mutations is emerging in the prognostication of myelofibrosis.
SUMMARY: A wide mutational analysis of MPN helps to define diagnosis and prognosis. In the future, clinical trials based on a robust valuation of mutations will guide treatment decision-making towards precision medicine.

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Year:  2016        PMID: 26825696     DOI: 10.1097/MOH.0000000000000218

Source DB:  PubMed          Journal:  Curr Opin Hematol        ISSN: 1065-6251            Impact factor:   3.284


  3 in total

Review 1.  Update from the latest WHO classification of MPNs: a user's manual.

Authors:  Francesco Passamonti; Margherita Maffioli
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

2.  Quality of life and symptom burden among myeloproliferative neoplasm patients: do symptoms impact quality of life?

Authors:  Blake T Langlais; Holly Geyer; Robyn Scherber; Ruben A Mesa; Amylou C Dueck
Journal:  Leuk Lymphoma       Date:  2018-07-22

Review 3.  Towards a Personalized Definition of Prognosis in Philadelphia-Negative Myeloproliferative Neoplasms.

Authors:  Barbara Mora; Francesco Passamonti
Journal:  Curr Hematol Malig Rep       Date:  2022-09-01       Impact factor: 4.213

  3 in total

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