2021
DOI: 10.1016/j.revmed.2020.08.018
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Les myélofibroses

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Cited by 5 publications
(2 citation statements)
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“…On February 28, 2022, the FDA granted accelerated approval to Pacritinib, a highly effective inhibitor of JAK2 and FMS-like tyrosine kinase 3 (FLT3), which was used to treat adult patients with low platelets who suffer from intermediate or high-risk primary or secondary myelofibrosis (MF) [ 127 , 128 ]. Pacritinib potently inhibits wild-type JAK2 (IC 50 = 23 nM), JAK2 V617F (IC 50 = 19 nM), FLT3 (IC 50 = 22 nM), and FLT3 D835Y (IC 50 = 6 nM) [ 129 ], which benefits the signaling of many growth factors and cytokines associated with immune and hematopoiesis function.…”
Section: Hematologic Drugsmentioning
confidence: 99%
“…On February 28, 2022, the FDA granted accelerated approval to Pacritinib, a highly effective inhibitor of JAK2 and FMS-like tyrosine kinase 3 (FLT3), which was used to treat adult patients with low platelets who suffer from intermediate or high-risk primary or secondary myelofibrosis (MF) [ 127 , 128 ]. Pacritinib potently inhibits wild-type JAK2 (IC 50 = 23 nM), JAK2 V617F (IC 50 = 19 nM), FLT3 (IC 50 = 22 nM), and FLT3 D835Y (IC 50 = 6 nM) [ 129 ], which benefits the signaling of many growth factors and cytokines associated with immune and hematopoiesis function.…”
Section: Hematologic Drugsmentioning
confidence: 99%
“…Other common mutations include those of calreticulin (CALR) and of myeloproliferative leukemia virus oncogene (MPL) which make up 25% and 7% of PMF cases, respectively [4]. These mutations are believed to start clonal myeloproliferation, leading to clinical presentation including anemia, hepatosplenomegaly, and systemic symptoms like fatigue, night sweats, and low-grade fever [5].…”
Section: Introductionmentioning
confidence: 99%