Nilotinib in patients with systemic mastocytosis: analysis of the phase 2, open-label, single-arm nilotinib registration study

作者：Hochhaus Andreas^*; Baccarani Michele; Giles Francis J; Le Coutre Philipp D; Mueller Martin C; Reiter Andreas; Santanastasio Helene; Leung Mimi; Novick Steven; Kantarjian Hagop M

来源：Journal of Cancer Research and Clinical Oncology, 2015, 141(11): 2047-2060.

DOI：10.1007/s00432-015-1988-0

• Nilotinib
• Tyrosine kinase inhibitor
• Systemic mastocytosis
• KIT D816V
• Aggressive systemic mastocytosis
• Indolent systemic mastocytosis

Activating KIT mutations are part of the pathogenesis of systemic mastocytosis (SM). Nilotinib is a tyrosine kinase inhibitor that potently inhibits activated forms of KIT. This phase 2, open-label, single-arm study (CAMN107A2101; evaluated nilotinib in patients with SM.
Patients with SM [aggressive SM (ASM), indolent SM, or other] received nilotinib 400 mg twice daily. C-findings were collected retrospectively to assess response using criteria proposed after trial initiation. Response was evaluated using improvements in laboratory findings (for all patients) and ASM response criteria (for the ASM subgroup).
In 61 patients enrolled, the median nilotinib exposure was 232 days (range 3-1274 days) with a median follow-up of 34.7 months. In patients with ASM (n = 37), the overall response rate was 21.6 %. In the eight responders, all of whom had a KIT D816V mutation at any time, mast cell infiltration and tryptase level decreased by 70 % and 29.8 %, respectively; absolute neutrophil count increased by 94.7 %. Laboratory parameters also improved in the non-ASM subgroups. Overall survival at 24 months was 81.2 % (95 % CI 70.6-91.8 %) with median survival not yet reached. New or worsening grade 3/4 hematologic adverse events (AEs) included thrombocytopenia (10.3 %), anemia (10.0 %), and neutropenia (6.9 %). The most common grade 3/4 nonhematologic drug-related AEs were diarrhea (6.6 %) and headache (4.9 %). Eleven patients (9 with ASM, 2 with MCL) died, 10 due to progressive disease; 7 deaths occurred a parts per thousand yen28 days after treatment discontinuation.
Nilotinib 400 mg twice daily was effective in some patients with SM, including patients with mutated KIT D816V.

• 出版日期2015-11