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Recent advances in the genomics and therapy of BCR/ABL1-positive and -negative chronic myeloproliferative neoplasms

  • Tariq I. Mughal(corresponding author)
    ,
  • Jason Gotlib
    ,
  • Ruben Mesa
    ,
  • Steffen Koschmieder
    ,
  • H. Jean Khoury
    ,
*Corresponding author for this work
  • Tufts University Medical Center
    ,
  • Stanford University
    ,
  • University of Texas Health Science Center at San Antonio
    ,
  • RWTH Aachen University
    ,
  • Emory University
    ,
  • University of Texas MD Anderson Cancer Center
Scholary Output:
Contribution to journal
Review article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

This review is based on the presentations and deliberations at the 7th John Goldman Chronic Myeloid Leukemia (CML) and Myeloproliferative Neoplasms (MPN) Colloquium which took place in Estoril, Portugal on the 15th October 2017, and the 11th post-ASH International Workshop on CML and MPN which took place on the 6th-7th December 2016, immediately after the 58th American Society of Hematology Annual Meeting. Rather than present a resume of the proceedings, we have elected to address some of the topical translational research and clinically relevant topics in greater detail. We address recent updates in the genetics and epigenetics of MPN, the mechanisms of transformation by mutant calreticulin, advances in the biology and therapy of systemic mastocytosis, clinical updates on JAK2 inhibitors and other therapeutic approaches for patients with MPNs, cardiovascular toxicity related to tyrosine kinase inhibitors and the concept of treatment-free remission for patients with CML.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 67-74 (8 pages)

Journal (Volume, Issue Number)

Leukemia Research (Volume 67)

Publication milestones

  • Published - 04/2018

Publication status

Published - 04/2018

ISSN

0145-2126

Publication IDs

  • Scopus: 85042214146
  • PubMed: 29466766

Publication metrics

Metrics

SciVal
FWCI
0.34
SciVal
Author count
16
SciVal
citations
6
SciVal
Paper percentile
70
Fractional count
1
Fractional count
0.06
Fractional count
15
Fractional count
0.94
Fractional count
1
Fractional count
1
Scopus
citations

PlumX, opens in new tab

Citation count
9
Captures
37

Funding Details

O Abdel-Wahab: No relevant disclosures. T Barbui: No relevant disclosures. J Cortes: Consultancy: Novartis, Bristol-Myers Squibb, Pfizer. Research funding: Novartis, Bristol-Myers Squibb, Pfizer. R Gale : Part-time employee Celgene Corp. J Gotlib: No relevant disclosures. R Hehlmann: Research funding: Bristol-Myers Squibb, Novartis. HJ Khoury: No relevant disclosures. S Koschmieder: Consultancy: Novartis, Bristol-Myers Squibb, Pfizer, Baxalta/CTI, AOP, Sanofi. Research funding: Novartis, Bristol-Myers Squibb, Novartis Foundation. R Mesa: Research funding: Incyte, Lilly, NS Pharma, Sanofi, Gilead, CTI, Genentech. TI Mughal: No relevant disclosures. G Saglio: Consultancy: Bristol-Myers Squibb; Research funding: Novartis. S Saussele: No relevant disclosures. RA Van Etten: Scientific Advisory Boards: Bristol Myers-Squibb, Pfizer, TEVA, Sunesis, Karyopharm; Research funding: TEVA, Verastem. S Verstovsek: Research funding: Incyte Corporation, Roche, Astrazeneca, Lilly Oncology, NS Pharma, Bristol Myers Squibb, Celgene, Gilead, Seattle Genetics, Promedior, CTI BioPharma Corp., Galena BioPharma, Pfizer, Genentech, Blueprint Medicines Corp.
FundersFunding number
Novartis Foundation
-
NCI
P30CA054174
BMS
-
Novartis
-