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Illuminating novel biological aspects and potential new therapeutic approaches for chronic myeloproliferative malignancies.
Mughal, Tariq I; Pemmaraju, Naveen; Psaila, Bethan; Radich, Jerald; Bose, Prithviraj; Lion, Thomas; Kiladjian, Jean-Jacques; Rampal, Raajit; Jain, Tania; Verstovsek, Srdnan; Yacoub, Abdulraheem; Cortes, Jorge E; Mesa, Ruben; Saglio, Giuseppe; van Etten, Richard A.
Afiliación
  • Mughal TI; Tufts University Medical Center, Boston, Massachusetts, USA.
  • Pemmaraju N; MD Anderson Cancer Center, Houston, Texas, USA.
  • Psaila B; MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Radich J; Frederick Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Bose P; MD Anderson Cancer Center, Houston, Texas, USA.
  • Lion T; Childrens Cancer Research Institute, Vienna, Austria.
  • Kiladjian JJ; Hôpital Saint-Louis, Université de Paris, Paris, France.
  • Rampal R; Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Jain T; Sidney Kimmel Cancer Center, John Hopkins Hospital, Baltimore, Maryland, USA.
  • Verstovsek S; MD Anderson Cancer Center, Houston, Texas, USA.
  • Yacoub A; Division of Hematologic Malignancies, University of Kansas, Kansas City, Kansas, USA.
  • Cortes JE; Georgia Cancer Center, Augusta University, Augusta, Georgia, USA.
  • Mesa R; Mays Cancer Center at UT Health San Antonio MD Anderson, San Antonio, Texas, USA.
  • Saglio G; Orbassano University Hospital, Turin, Italy.
  • van Etten RA; University of California Irvine, Irvine, California, USA.
Hematol Oncol ; 38(5): 654-664, 2020 Dec.
Article en En | MEDLINE | ID: mdl-32592408
This review reflects the presentations and discussion at the 14th post-American Society of Hematology (ASH) International Workshop on Chronic Myeloproliferative Malignancies, which took place on the December 10 and 11, 2019, immediately after the 61st ASH Annual Meeting in Orlando, Florida. Rather than present a resume of the proceedings, we address some of the topical translational science research and clinically relevant topics in detail. We consider how recent studies using single-cell genomics and other molecular methods reveal novel aspects of hematopoiesis which in turn raise the possibility of new therapeutic approaches for patients with myeloproliferative neoplasms (MPNs). We discuss how alternative therapies could benefit patients with chronic myeloid leukemia who develop BCR-ABL1 mutant subclones following ABL1-tyrosine kinase inhibitor therapy. In MPNs, we focus on efforts beyond JAK-STAT and the merits of integrating activin receptor ligand traps, interferon-α, and allografting in the current treatment algorithm for patients with myelofibrosis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva / Susceptibilidad a Enfermedades / Trastornos Mieloproliferativos Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Hematol Oncol Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva / Susceptibilidad a Enfermedades / Trastornos Mieloproliferativos Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Hematol Oncol Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos