联邦拉替尼在中-2或高危骨髓纤维化患者中的暴露-反应关系。

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Yizhe Chen, Yan Li, Yongjun Xue, Patrick Brown, Christopher Hernandez, Shelonitda Rose, Richard Pilot, Gopal Krishna, Ken Ogasawara
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引用次数: 0

摘要

目的:federatinib是一种有效的口服Janus激酶抑制剂,用于治疗骨髓纤维化(MF)。本报告描述了联邦拉替尼的暴露-反应(E-R)分析,该分析基于中2或高风险MF患者的2/3期研究汇总数据,既往有或没有鲁索利替尼暴露。方法:药代动力学(PK)暴露量来源于人群PK分析。疗效终点包括脾体积缩小≥35% (SVR35)和总症状评分缩小≥50% (TSS缓解)。安全性终点包括≥3级贫血或血小板减少症,任何级别的恶心/呕吐和腹泻。E-R模型采用逻辑回归分析。结果:fdratinib暴露与SVR35呈正相关(优势比[OR], 38.2;95%置信区间[CI], 12.4-118;p9 /L)与经历≥3级贫血相关(P结论:Fedratinib暴露与脾脏体积缩小和TSS反应呈正相关,对安全性没有显著影响。无论鲁索利替尼是否暴露,联邦拉替尼400mg每日一次是MF患者的适当剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exposure-response relationship of fedratinib in patients with intermediate-2 or high-risk myelofibrosis.

Aims: Fedratinib is a potent, oral, Janus kinase inhibitor for the treatment of myelofibrosis (MF). This report describes exposure-response (E-R) analyses of fedratinib based on pooled data from phase 2/3 studies in patients with intermediate-2 or high-risk MF, with or without prior ruxolitinib exposure.

Methods: Pharmacokinetic (PK) exposures were derived from the population PK analysis. Efficacy endpoints included spleen volume reduction ≥35% (SVR35) and total symptom score reduction ≥50% (TSS response). Safety endpoints included grade ≥3 anaemia or thrombocytopenia, any-grade nausea/vomiting and diarrhoea. The E-R models were developed using logistic regression analyses.

Results: Fedratinib exposure was positively associated with SVR35 (odds ratio [OR], 38.2; 95% confidence interval [CI], 12.4-118; P < 0.001) and TSS response (OR, 20.8; 95% CI, 6.27-69.2; P < 0.001), after adjusting for covariates. Baseline spleen volume was inversely associated with SVR35 (P = 0.029). Prior ruxolitinib exposure was not associated with SVR35 (P = 0.090) or TSS response (P = 0.326). Although numerically higher incidence of adverse events was observed in patients with higher fedratinib exposure, there was no statistically significant association between fedratinib exposure and any safety related endpoints. Prior ruxolitinib exposure was associated with experiencing grade ≥3 thrombocytopenia (P = 0.004). Lower baseline haemoglobin level (<10 g/dL) and platelet count (<100 × 109/L) were associated with experiencing grade ≥3 anaemia (P < 0.001) and thrombocytopenia (P < 0.001), respectively. Antiemetic prophylaxis was associated with lower rates of nausea/vomiting (P < 0.001).

Conclusions: Fedratinib exposure was positively associated with spleen volume reduction and TSS responses, without having significant impact on safety. Fedratinib 400 mg once daily is an appropriate dose for patients with MF regardless of ruxolitinib exposure.

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来源期刊
CiteScore
6.30
自引率
8.80%
发文量
419
审稿时长
1 months
期刊介绍: Published on behalf of the British Pharmacological Society, the British Journal of Clinical Pharmacology features papers and reports on all aspects of drug action in humans: review articles, mini review articles, original papers, commentaries, editorials and letters. The Journal enjoys a wide readership, bridging the gap between the medical profession, clinical research and the pharmaceutical industry. It also publishes research on new methods, new drugs and new approaches to treatment. The Journal is recognised as one of the leading publications in its field. It is online only, publishes open access research through its OnlineOpen programme and is published monthly.
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