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Olutasidenib(FT-2102)诱导复发或难治性 IDH1 突变 AML 患者获得持久完全缓解。

Olutasidenib (FT-2102) induces durable complete remissions in patients with relapsed or refractory IDH1-mutated AML.

机构信息

Hematologie Clinique, Institut Gustave Roussy, Villejuif, France.

Département (DMU) d'hématologie et immunologie, APHP Nord, Service d'hématologie séniors, Hôpital St Louis/université de Paris, Paris, France.

出版信息

Blood Adv. 2023 Jul 11;7(13):3117-3127. doi: 10.1182/bloodadvances.2022009411.

Abstract

Olutasidenib (FT-2102) is a potent, selective, oral, small-molecule inhibitor of mutant isocitrate dehydrogenase 1 (mIDH1). Overall, 153 IDH1 inhibitor-naive patients with mIDH1R132 relapsed/refractory (R/R) acute myeloid leukemia (AML) received olutasidenib monotherapy 150 mg twice daily in the pivotal cohort of this study. The median age of participants was 71 years (range, 32-87 years) and the median number of prior regimens received by patients was 2 (1-7). The rate of complete remission (CR) plus CR with partial hematologic recovery (CRh) was 35%, and the overall response rate was 48%. Response rates were similar in patients who had, and who had not, received prior venetoclax. With 55% of patients censored at the time of data cut-off, the median duration of CR/CRh was 25.9 months. The median duration of overall response was 11.7 months, and the median overall survival was 11.6 months. Of 86 patients who were transfusion dependent at baseline, a 56-day transfusion independence was achieved in 29 (34%), which included patients in all response groups. Grade 3 or 4 treatment-emergent adverse events (≥10%) were febrile neutropenia and anemia (n = 31; 20% each), thrombocytopenia (n = 25; 16%), and neutropenia (n = 20; 13%). Differentiation syndrome adverse events of special interest occurred in 22 (14%) patients, with 14 (9%) grade ≥3 and 1 fatal case reported. Overall, olutasidenib induced durable remissions and transfusion independence with a well-characterized and manageable side effect profile. The observed efficacy represents a therapeutic advance in this molecularly defined, poor-prognostic population of patients with mIDH1 R/R AML. This trial was registered at www.clinicaltrials.gov as #NCT02719574.

摘要

奥拉帕尼(FT-2102)是一种有效的、选择性的、口服的、小分子突变型异柠檬酸脱氢酶 1(mIDH1)抑制剂。在这项研究的关键队列中,153 名 IDH1 抑制剂初治伴 mIDH1R132 复发/难治性(R/R)急性髓系白血病(AML)患者接受奥拉帕尼单药治疗,每日两次,每次 150mg。参与者的中位年龄为 71 岁(范围为 32-87 岁),患者接受的中位数治疗方案为 2 种(1-7 种)。完全缓解(CR)加部分血液学恢复(CRh)的缓解率为 35%,总缓解率为 48%。在接受和未接受维奈托克治疗的患者中,缓解率相似。在数据截止时,55%的患者被排除在外,CR/CRh 的中位持续时间为 25.9 个月。总反应的中位持续时间为 11.7 个月,总生存时间为 11.6 个月。在基线时依赖输血的 86 名患者中,有 29 名(34%)实现了 56 天的输血独立性,包括所有反应组的患者。≥10%的 3 级或 4 级治疗相关不良事件为发热性中性粒细胞减少症和贫血(n=31;各占 20%)、血小板减少症(n=25;16%)和中性粒细胞减少症(n=20;13%)。特别关注的分化综合征不良事件发生在 22 名(14%)患者中,其中 14 名(9%)为 3 级及以上,1 例死亡。总的来说,奥拉帕尼诱导了持久的缓解和输血独立性,具有特征明确且可管理的副作用谱。观察到的疗效代表了在这种分子定义的、预后不良的伴 mIDH1 R/R AML 患者群体中的治疗进展。该试验在 www.clinicaltrials.gov 上注册为#NCT02719574。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69bf/10362540/5bc4166e5ea4/BLOODA_ADV-2022-009411-fx1.jpg

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