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关于无效性监测的评论。

A comment on futility monitoring.

作者信息

Freidlin Boris, Korn Edward L

机构信息

Biometric Research Branch, National Cancer Institute, Bethesda, MD 20892, USA.

出版信息

Control Clin Trials. 2002 Aug;23(4):355-66. doi: 10.1016/s0197-2456(02)00218-0.

Abstract

Futility monitoring of randomized clinical trials is becoming widely used. In this paper we discuss several concerns associated with aggressive monitoring for lack of activity in studies comparing experimental and control treatment arms: (1) stopping for futility when the experimental arm is doing better than the control arm, (2) conditional power not being low at the time of stopping, (3) potential loss of power to detect clinically interesting differences that are smaller than the design alternative, and (4) sensitivity of the power to the departure from the proportional hazards assumption. Our investigation suggests that aggressive futility rules do not generally reduce power (relative to less aggressive rules) under incorrect design assumptions such as overstatement of the target treatment effect or mild violations of the proportional hazards assumption. On the other hand, aggressive monitoring rules may result in an early termination for futility when the experimental arm is doing better than the control arm (in some cases nontrivially better, especially when trials are designed for unrealistically large effects). Thus, aggressive monitoring rules may fail to provide sufficiently convincing evidence to influence clinical practice or to establish a standard of treatment.

摘要

随机临床试验的无效性监测正被广泛应用。在本文中,我们讨论了与在比较试验组和对照组治疗效果的研究中积极监测无效性相关的几个问题:(1)当试验组比对照组表现更好时因无效性而停止试验;(2)停止试验时条件把握度不低;(3)检测小于设计替代值的临床有意义差异的把握度可能丧失;(4)把握度对偏离比例风险假设的敏感性。我们的研究表明,在诸如夸大目标治疗效果或轻微违反比例风险假设等错误设计假设下,积极的无效性规则通常不会降低把握度(相对于不太积极的规则)。另一方面,当试验组比对照组表现更好时(在某些情况下好很多,尤其是当试验设计的效果不切实际地大时),积极的监测规则可能会因无效性而导致试验提前终止。因此,积极的监测规则可能无法提供足够有说服力的证据来影响临床实践或确立治疗标准。

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