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阿伐普利替尼对比最佳可用疗法治疗晚期系统性肥大细胞增多症的疗效。

Efficacy of avapritinib versus best available therapy in the treatment of advanced systemic mastocytosis.

机构信息

Department of Hematology and Oncology, University Hospital Mannheim, Mannheim, Germany.

Stanford Cancer Institute/Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Leukemia. 2022 Aug;36(8):2108-2120. doi: 10.1038/s41375-022-01615-z. Epub 2022 Jul 5.

Abstract

Advanced systemic mastocytosis (AdvSM) is a rare myeloid neoplasm associated with poor overall survival (OS). This study (NCT04695431) compared clinical outcomes between patients with AdvSM treated with avapritinib in the Phase 1 EXPLORER (NCT0256198) and Phase 2 PATHFINDER (NCT03580655) trials (N = 176) and patients treated with best available therapy (BAT; N = 141). A multi-center, observational, retrospective chart review study was conducted at six study sites (four European, two American) to collect data from patients with AdvSM who received BAT; these data were pooled with data from EXPLORER and PATHFINDER. Comparisons between outcomes of OS, duration of treatment (DOT), and maximum reduction in serum tryptase were conducted between the treatment cohorts, with adjustment for key covariates. The results indicated that the avapritinib cohort had significantly better survival (adjusted hazard ratio (HR) (95% confidence interval (CI)): 0.48 (0.29, 0.79); p = 0.004) and significantly longer DOT (HR: 0.36 (0.26, 0.51); p < 0.001) compared to the BAT cohort. Additionally, the mean difference in percentage maximum reduction in serum tryptase levels was 60.3% greater in the avapritinib cohort (95% CI: -72.8, -47.9; p < 0.001). With no randomized controlled trials comparing avapritinib to BAT, these data offer crucial insights into the improved efficacy of avapritinib for the treatment of AdvSM.

摘要

高级系统性肥大细胞增多症(AdvSM)是一种与总体生存(OS)较差相关的罕见骨髓增生性肿瘤。这项研究(NCT04695431)比较了接受 avapritinib 治疗的 AdvSM 患者(EXPLORER 期,NCT0256198 和 PATHFINDER 期,NCT03580655,N = 176)与接受最佳可用治疗(BAT;N = 141)的患者的临床结果。在六个研究地点(四个欧洲,两个美国)进行了一项多中心、观察性、回顾性图表审查研究,以收集接受 BAT 的 AdvSM 患者的数据;这些数据与 EXPLORER 和 PATHFINDER 的数据合并。在调整了关键协变量后,对 OS 结果、治疗持续时间(DOT)和血清胰蛋白酶最大降低的比较进行了治疗组之间的比较。结果表明,与 BAT 队列相比,avapritinib 队列的生存明显更好(调整后的风险比(HR)(95%置信区间(CI)):0.48(0.29,0.79);p = 0.004),DOT 明显更长(HR:0.36(0.26,0.51);p < 0.001)。此外,avapritinib 队列中血清胰蛋白酶水平最大降低的平均差异百分比高出 60.3%(95%CI:-72.8,-47.9;p < 0.001)。由于没有随机对照试验比较 avapritinib 与 BAT,这些数据为 avapritinib 治疗 AdvSM 的疗效改善提供了关键的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fd/9343245/6770d3763e36/41375_2022_1615_Fig1_HTML.jpg

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