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达菲林(一种促性腺激素释放激素受体拮抗剂)治疗前列腺癌对健康男性心脏复极的影响:一项随机、安慰剂和阳性对照全面 QT/QTc 临床试验

Effect of Degarelix, a Gonadotropin-Releasing Hormone Receptor Antagonist for the Treatment of Prostate Cancer, on Cardiac Repolarisation in a Randomised, Placebo and Active Comparator Controlled Thorough QT/QTc Trial in Healthy Men.

机构信息

Ferring Pharmaceuticals A/S, Kay Fiskers Plads 11, 2100, Copenhagen, Denmark.

Novo Nordisk A/S, Copenhagen, Denmark.

出版信息

Clin Drug Investig. 2017 Sep;37(9):873-879. doi: 10.1007/s40261-017-0547-7.

Abstract

BACKGROUND AND OBJECTIVES

Degarelix is a gonadotropin-releasing hormone antagonist registered for the treatment of advanced hormone-dependent prostate cancer. Treatment causing androgen deprivation is associated with QT prolongation and this study investigated whether degarelix at supratherapeutic concentrations has an intrinsic effect per se on cardiac repolarisation and the QT interval.

METHODS

This was a single-centre, randomised, crossover study comparing the effect of degarelix, placebo, and the positive control moxifloxacin on the QT interval. Degarelix and placebo treatments were double-blind, whereas moxifloxacin treatment was open-label. Eighty healthy men, aged 18-45 years, received single intravenous doses of degarelix 2.8 mg, and placebo, as well as a single oral dose of moxifloxacin 400 mg. Electrocardiograms were collected up to 24 h after the start of administration, with the QT interval assessed and plasma concentrations of degarelix concomitantly analysed.

RESULTS

Time-matched, one-sided 95% upper confidence boundaries for baseline-corrected average changes from placebo for the QT interval, corrected using the Fridericia method (ΔΔQTcF), did not exceed 10 ms at any timepoint, with maximum degarelix concentrations reaching approximately threefold the concentrations seen in the treatment of prostate cancer. Furthermore, concentration-exposure analysis indicated absence of any QT prolongation effects of degarelix. No significant effect on any other cardiac parameter was observed. The lower bound of the 98.3% confidence interval for moxifloxacin ΔΔQTcF exceeded 5 ms, thus verifying assay sensitivity.

CONCLUSION

The results showed that the study was validated to detect a significant effect on the QT interval, and that degarelix by itself does not have any effect on the QT interval and cardiac repolarisation at supratherapeutic concentrations.

摘要

背景与目的

地加瑞克是一种促性腺激素释放激素拮抗剂,用于治疗晚期激素依赖性前列腺癌。导致雄激素剥夺的治疗与 QT 间期延长有关,本研究旨在探讨超治疗浓度的地加瑞克本身是否对心脏复极和 QT 间期有内在影响。

方法

这是一项单中心、随机、交叉研究,比较了地加瑞克、安慰剂和阳性对照莫西沙星对 QT 间期的影响。地加瑞克和安慰剂治疗为双盲,而莫西沙星治疗为开放标签。80 名年龄在 18-45 岁的健康男性接受了单次静脉注射地加瑞克 2.8mg 和安慰剂,以及单次口服莫西沙星 400mg。给药开始后 24 小时内采集心电图,评估 QT 间期,并同时分析地加瑞克的血浆浓度。

结果

以时间为匹配的单侧 95%置信区间上限,用 Fridericia 法校正(ΔΔQTcF),地加瑞克与安慰剂相比,在任何时间点的平均变化均未超过 10ms,最大地加瑞克浓度约为治疗前列腺癌时的 3 倍。此外,浓度-暴露分析表明地加瑞克没有延长 QT 间期的作用。未观察到地加瑞克对任何其他心脏参数有显著影响。莫西沙星 ΔΔQTcF 的 98.3%置信区间下限超过 5ms,从而验证了检测方法的灵敏度。

结论

结果表明,该研究验证了检测 QT 间期显著影响的能力,并且在超治疗浓度下,地加瑞克本身对地加瑞克和心脏复极没有任何影响。

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