Durable response to lenalidomide in a patient with myelodysplastic syndrome associated with isolated 5q deletion and JAK2 V617F mutation despite discontinuation of treatment

Loss of a section of the long arm of chromosome 5, as a sole cytogenetic abnormality, characterizes a rare type of myelodysplastic syndrome [del(5q) MDS] and the co-existence of the JAK2 V617F mutation occurs in a small subset of these cases. Patients with isolated del(5q) MDS have a relatively favo...

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Vydáno v:Mol Clin Oncol
Hlavní autoři: HATZIMICHAEL, ELEFTHERIA, LAGOS, KONSTANTINOS, VASSOU, AMALIA, GOUGOPOULOU, DORA, PAPOUDOU-BAI, ALEXANDRA, BRIASOULIS, EVANGELOS
Médium: Artigo
Jazyk:Inglês
Vydáno: D.A. Spandidos 2016
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4906970/
https://ncbi.nlm.nih.gov/pubmed/27330758
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mco.2016.866
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