BRAF inhibition in refractory hairy-cell leukemia

To the Editor: Hairy-cell leukemia (HCL) is a mature B-cell lymphoid cancer that is commonly treated with purine analogues.1 Virtually all patients with HCL carry the BRAF V600E mutation, which constitutively activates the MEK-ERK pathway and which can be inhibited in vitro by the mutation-specific...

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Main Authors: Dietrich, Sascha (Author) , Glimm, Hanno (Author) , Andrulis, Mindaugas (Author) , Kalle, Christof von (Author) , Ho, Anthony Dick (Author) , Zenz, Thorsten (Author)
Format: Article (Journal)
Language:English
Published: May 24, 2012
In: The New England journal of medicine
Year: 2012, Volume: 366, Issue: 21, Pages: 2038-2040
ISSN:1533-4406
DOI:10.1056/NEJMc1202124
Online Access:Verlag, Volltext: http://dx.doi.org/10.1056/NEJMc1202124
Verlag, Volltext: https://doi.org/10.1056/NEJMc1202124
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Author Notes:Sascha Dietrich, Hanno Glimm, Mindaugas Andrulis, Christof von Kalle, Anthony D. Ho, Thorsten Zenz
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Summary:To the Editor: Hairy-cell leukemia (HCL) is a mature B-cell lymphoid cancer that is commonly treated with purine analogues.1 Virtually all patients with HCL carry the BRAF V600E mutation, which constitutively activates the MEK-ERK pathway and which can be inhibited in vitro by the mutation-specific BRAF inhibitor PLX-4720.2 BRAF mutations have been identified in melanoma but are found across cancers.3 An inhibitor of mutated BRAF (vemurafenib) has transformed the treatment of melanoma. It is unclear whether this clinical efficacy can be extrapolated to other cancers.4,5 We used vemurafenib in a patient with refractory HCL and a pressing need for . . .
Item Description:Gesehen am 29.03.2018
Physical Description:Online Resource
ISSN:1533-4406
DOI:10.1056/NEJMc1202124