Literature DB >> 30333119

How I treat the blast phase of Philadelphia chromosome-negative myeloproliferative neoplasms.

Olatoyosi Odenike1.   

Abstract

The classic Philadelphia chromosome (Ph)-negative myeloproliferative neoplasms (MPNs) are a heterogeneous group of hematopoietic stem-cell diseases, characterized by activated JAK/STAT signaling and significant phenotypic mimicry, including a propensity for evolution to myeloid blast phase disease. Effective therapeutic options are limited for patients with Ph- MPNs in the blast phase (MPN-BP), and allogeneic stem-cell transplantation is the only known cure. Our increasing understanding of the molecular pathogenesis of this group of diseases, coupled with the increasing availability of targeted agents, has the potential to inform new subset-specific therapeutic approaches. Ultimately, progress in MPN-BP will hinge on prospective clinical and translational investigations with the goal of generating more effective treatment interventions. This case-based review highlights the molecular and clinical heterogeneities of MPN-BP and incorporates a treatment algorithm that underscores the importance of a personalized approach to this challenging group of diseases.
© 2018 by The American Society of Hematology.

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Year:  2018        PMID: 30333119     DOI: 10.1182/blood-2018-03-785907

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  8 in total

1.  Genetic factors rather than blast reduction determine outcomes of allogeneic HCT in BCR-ABL-negative MPN in blast phase.

Authors:  Vikas Gupta; James A Kennedy; Jose-Mario Capo-Chichi; Soyoung Kim; Zhen-Huan Hu; Edwin P Alyea; Uday R Popat; Ronald M Sobecks; Bart L Scott; Aaron T Gerds; Rachel B Salit; H Joachim Deeg; Ryotara Nakamura; Wael Saber
Journal:  Blood Adv       Date:  2020-11-10

Review 2.  Genomics of MPN progression.

Authors:  Anand A Patel; Olatoyosi Odenike
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2020-12-04

3.  A phase 1 study of azacitidine with high-dose cytarabine and mitoxantrone in high-risk acute myeloid leukemia.

Authors:  Kirk E Cahill; Yasmin H Karimi; Theodore G Karrison; Nitin Jain; Margaret Green; Howard Weiner; Noreen Fulton; Sabah Kadri; Lucy A Godley; Andrew S Artz; Hongtao Liu; Michael J Thirman; Michelle M Le Beau; Megan E McNerney; Jeremy Segal; Richard A Larson; Wendy Stock; Olatoyosi Odenike
Journal:  Blood Adv       Date:  2020-02-25

Review 4.  Accelerated Phase of Myeloproliferative Neoplasms.

Authors:  Omar A Shahin; Helen T Chifotides; Prithviraj Bose; Lucia Masarova; Srdan Verstovsek
Journal:  Acta Haematol       Date:  2021-04-21       Impact factor: 2.195

Review 5.  Patterns of Ruxolitinib Therapy Failure and Its Management in Myelofibrosis: Perspectives of the Canadian Myeloproliferative Neoplasm Group.

Authors:  Vikas Gupta; Sonia Cerquozzi; Lynda Foltz; Christopher Hillis; Rebecca Devlin; Mahmoud Elsawy; Kuljit Grewal; Caroline Hamm; Caroline McNamara; Shireen Sirhan; Brian Leber
Journal:  JCO Oncol Pract       Date:  2020-03-05

Review 6.  Myelofibrosis in 2019: moving beyond JAK2 inhibition.

Authors:  Michael Schieber; John D Crispino; Brady Stein
Journal:  Blood Cancer J       Date:  2019-09-11       Impact factor: 11.037

7.  Outcome of patients with IDH1/2-mutated post-myeloproliferative neoplasm AML in the era of IDH inhibitors.

Authors:  Helen T Chifotides; Lucia Masarova; Mansour Alfayez; Naval Daver; Yesid Alvarado; Elias Jabbour; Marina Konopleva; Hagop M Kantarjian; Keyur P Patel; Courtney D DiNardo; Srdan Verstovsek
Journal:  Blood Adv       Date:  2020-11-10

8.  An agenda for future research projects in polycythemia vera and essential thrombocythemia.

Authors:  Tiziano Barbui; Alessandro Maria Vannucchi; Paola Guglielmelli; Valerio De Stefano; Alessandro Rambaldi
Journal:  Haematologica       Date:  2020-05-28       Impact factor: 9.941

  8 in total

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