局部晚期基底细胞癌患者停止索尼替吉治疗后的疗效:BOLT 42个月分析结果

Michael Migden, M. Kheterpal, Brent Moody, Kunal Patel, Leonard Lionnet, Sakthivel Sivam, Joe Conti, N. Squittieri, Aaron Farberg
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摘要

简介:索尼替吉(Sonidegib)是一种刺猬(HH)通路抑制剂,已被批准用于治疗无法接受根治性手术或放射治疗的局部晚期基底细胞癌(laBCC)。为期 42 个月的关键性 BOLT(NCT01327053)研究表明,索尼替吉具有持续的疗效和可控的安全性。之前进行的为期 18 个月的分析表明,临床获益在索尼替吉停药后仍能持续。药代动力学模型表明,HH 通路抑制作用在停药后仍可维持。本分析报告介绍了索尼吉布(sonidegib)200 毫克/天对 LaBCC 患者的疗效,这些患者在停药 42 个月(研究结束)后未出现疾病进展 (PD)。研究方法BOLT是一项随机、双盲、安慰剂对照的2期研究。客观反应率(ORRs;完全反应+部分反应)、反应持续时间(DOR)和无进展生存期(PFS)由中央和研究者根据实体瘤改良反应评价标准(mRECIST)进行审查评估。此外,还对不良事件(AEs)进行了评估。结果:在随机接受索尼替吉每天200毫克治疗的66例laBCC患者中,有37例患者在没有PD的情况下中断了治疗。根据中央审查(57% [n = 20])和研究者审查(73% [n = 27]),这些患者的ORR与总体患者相似(根据中央审查和研究者审查,ORR分别为61% [n = 40]和71% [n = 47])。对于中断治疗的患者,中央审查和研究者审查的 DOR 中位数(95% 置信区间 [CI])分别为不可估计(NE)和 20.2 个月(12.0,NE)。中央审查和研究者审查的 PFS 中位数(95% 置信区间 [CI])分别为 NE 和 22.0 个月(16.6 个月,NE)。大多数 AE 的严重程度为 1/2 级。结论在这项为期42个月的分析中,每天接受索尼替吉200毫克治疗的laBCC患者在研究期间停药后仍能观察到临床获益。
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Efficacy Following Discontinuation of Sonidegib Treatment in Patients With Locally Advanced Basal Cell Carcinoma: Results From the BOLT 42-Month Analysis
Introduction: Sonidegib, a Hedgehog (HH) pathway inhibitor, is approved for the treatment of locally advanced basal cell carcinoma (laBCC) not amenable to curative surgery or radiation. The pivotal 42-month BOLT (NCT01327053) study demonstrated sustained efficacy and manageable safety of sonidegib. Prior analyses at 18 months demonstrated clinical benefit persisting beyond sonidegib discontinuation. Pharmacokinetic modeling suggests HH pathway inhibition can be maintained following discontinuation. This analysis presents the efficacy of sonidegib 200 mg daily in patients with laBCC who discontinued treatment without disease progression (PD) at 42 months (end of study). Methods: BOLT was a randomized, double-blind, placebo-controlled, Phase 2 study. Objective response rates (ORRs; complete response + partial response), duration of response (DOR), and progression-free survival (PFS) were assessed by central and investigator review per modified response evaluation criteria in solid tumors (mRECIST). Adverse events (AEs) were also assessed. Results: Of the 66 patients with laBCC randomized to sonidegib 200 mg daily, 37 discontinued treatment without PD. The ORRs for these patients per central (57% [n = 20]) and investigator (73% [n = 27]) review were similar to the overall patient population (61% [n = 40] and 71% [n = 47] per central and investigator review, respectively). For patients who discontinued treatment, the median (95% confidence interval [CI]) DOR per central and investigator review was not estimable (NE) and 20.2 months (12.0, NE), respectively. The median PFS (95% CI) per central and investigator review was NE and 22.0 months (16.6, NE), respectively. Most AEs were Grades 1/2 in severity. Conclusion: In this 42-month analysis among patients with laBCC who received sonidegib 200 mg daily, clinical benefit was observed beyond treatment discontinuation during this study.
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