Új utak a hajas sejtes leukémia és a rokon kórképek diagnosztikájában és kezelésében

Eszter Sári, Hajnalka Rajnai, Kitti Dénes, Csaba Bödör, Judit Csomor, Gábor Körösmezey, Ilona Tárkányi, Hanna Eid, Zsolt Nagy, J. Demeter

Research output: Review article

1 Citation (Scopus)

Abstract

Differential diagnosis of hairy cell leukemia (HCL) and related disorders (hairy cell leukemia variant and splenic marginal zone lymphoma) is of utmost importance since the treatment and prognosis of these lymphomas differ. Since 2011 diagnosis of hairy cell leukemia has been easier because of discovery of the disease defining somatic mutation BRAF V600E mutation, which has been also known as driver mutation in malignant melanoma. The presence of this mutation enabled targeted molecular therapy in HCL as well. As first line therapy purine nucleoside analogues are the gold standard, but refractory/relapsed patient are candidates for targeted BRAF-inhibitor therapy. This manuscript serves as guidance in making diagnosis and standard treatment of HCL, and summarizes newest data about molecular therapy, including our single center experience collected from 75 patients.

Original languageHungarian
Pages (from-to)137-144
Number of pages8
JournalMagyar Onkologia
Volume60
Issue number2
Publication statusPublished - jún. 6 2016

    Fingerprint

ASJC Scopus subject areas

  • Oncology

Cite this

Sári, E., Rajnai, H., Dénes, K., Bödör, C., Csomor, J., Körösmezey, G., Tárkányi, I., Eid, H., Nagy, Z., & Demeter, J. (2016). Új utak a hajas sejtes leukémia és a rokon kórképek diagnosztikájában és kezelésében. Magyar Onkologia, 60(2), 137-144.