| Literature DB >> 33799933 |
Aneta Szudy-Szczyrek1, Oliwia Bachanek-Mitura1, Tomasz Gromek1, Karolina Chromik2, Andrzej Mital3, Michał Szczyrek4, Witold Krupski5, Justyna Szumiło6, Zuzanna Kanduła7, Grzegorz Helbig2, Marek Hus1.
Abstract
In April 2017 midostaurin was approved by the US Food and Drug Administration for the treatment of patients with aggressive systemic mastocytosis (ASM). So far, very limited real world data on its efficacy is available. Thirteen patients aged from 48 to 79 years, who received midostaurin in the early access program, were included in the study. Midostaurin was used both in first (n = 5) and subsequent lines of treatment (n = 8). The median duration of exposure was 9 months. Most patients (77%, n = 10) had a clinical improvement already as soon as the second month of therapy. Objective response was noted in 4 (50%) of eight evaluated patients. Among responders, we observed a decrease in serum tryptase level (median 74.14%) and bone marrow infiltration by mast cells (median 50%) in the sixth month of treatment. In one case, in the 10th month of treatment, allogenic stem cell transplantation was performed, achieving complete remission. Five patients died, three due to progression of disease, one in the course of secondary acute myeloid leukemia and one due to reasons not related to mastocytosis. Treatment is ongoing in seven patients. We found that midostaurin therapy is beneficial to patients with ASM.Entities:
Keywords: KIT D816V mutation; aggressive systemic mastocytosis; mast cells; midostaurin; tryptase
Year: 2021 PMID: 33799933 PMCID: PMC7961806 DOI: 10.3390/jcm10051109
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241