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1.
Pathol Oncol Res ; 29: 1611378, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-38025907

RESUMEN

Introduction: Hairy cell leukemia (HCL) is an indolent B-cell lymphoproliferative disease. BRAF V600E mutation is detected in nearly all classical HCL cases which offers the possibility of targeted therapy. Objective: The aim of our study was to assess the efficacy of low-dose vemurafenib as well as to assess the long term outcome of HCL patients treated with this drug at the Department of Internal Medicine and Oncology at Semmelweis University. Methods: We report on 10 patients with classical HCL treated with low-dose vemurafenib at our Department between 2013 and 2022. Results: As a result of fixed time low-dose vemurafenib treatment, 5 of 10 patients (5/10) achieved partial remission, 4 (4/10) had stable disease, and 1 (1/10) had MRD positivity. No patients achieved complete remission. The median progression-free survival was 28.5 months while the overall survival was 82 months. Conclusion: We confirm that low dose of vemurafenib is effective and safe in the vast majority of patients with HCL. This small-molecule oral treatment allows to gain valuable time-months or even years-before further, usually parenteral treatment options have to be given or before previous treatment has to be repeated. There are also promising data supporting the combination of vemurafenib with other drugs for the treatment of HCL patients which could provide even further possibility to bridge treatment.


Asunto(s)
Antineoplásicos , Leucemia de Células Pilosas , Humanos , Vemurafenib/uso terapéutico , Leucemia de Células Pilosas/tratamiento farmacológico , Leucemia de Células Pilosas/genética , Antineoplásicos/uso terapéutico , Estudios de Seguimiento , Universidades , Proteínas Proto-Oncogénicas B-raf/genética
2.
Pathol Oncol Res ; 28: 1610338, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35570843

RESUMEN

Hairy cell leukaemia (HCL) is a rare B cell malignancy with an indolent course leading to pancytopaenia due to bone marrow infiltration. It has been proposed that HCL patients are at risk of developing a secondary malignancy, with a marked likelihood of the development of other hematologic malignancies including Hodgkin lymphoma and high-grade non-Hodgkin lymphomas. Here, we present the case of two patients who developed diffuse large B cell lymphoma after a long course of hairy cell leukaemia. In the case of the female patient, we report on the occurrence of a third malignant disease, which is very uncommon. With our case descriptions we contribute to the very small number of similar cases reported.


Asunto(s)
Leucemia de Células Pilosas , Linfoma de Células B Grandes Difuso , Linfoma no Hodgkin , Linfocitos B/patología , Médula Ósea/patología , Femenino , Humanos , Leucemia de Células Pilosas/complicaciones , Leucemia de Células Pilosas/patología , Linfoma de Células B Grandes Difuso/patología , Linfoma no Hodgkin/patología
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