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Two-treatment comparison based on joint toxicity and efficacy ordered alternatives in cancer trials.

机译:基于联合毒性和疗效的两种治疗方法比较在癌症试验中提出了替代方案。

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The primary goal of anticancer treatments is to attain efficacy, however toxicity could affect the course of the therapy. Methods have been proposed for comparing two treatments on the basis of the joint distribution for safety and efficacy outcomes, but they do not take into account the cumulative doses of drugs (chemotherapy) or radiation (radiotherapy) received by each patient. Moreover, these methods assume a parametric form for the joint distribution. In this paper we define a multi-dimensional parameter including toxicity and efficacy outcomes and the dose at which one, none or both occur. Each patient is classified into an ordered category depending on the order of occurrence of these two criteria: the sooner the patient benefits from efficacy and/or the later he/she experiences toxicity, the better is the treatment. We then apply likelihood ratio tests with ordered alternatives. This procedure requires constrained maximum likelihood estimation via isotonic regression. A large set of simulationscompares the proposed tests to other more usual tests and the results show a good power and a satisfactory type I error control. Our approach is illustrated with a multi-centre randomized clinical trial involving patients with metastatic non-seminomatous germ cell tumours. Copyright 2003 John Wiley & Sons, Ltd.
机译:抗癌治疗的主要目标是获得疗效,但是毒性可能会影响治疗过程。已经提出了基于关节分布的安全性和有效性结果比较两种治疗方法的方法,但是它们没有考虑每个患者接受的累积剂量的药物(化学疗法)或放射线(放射疗法)。此外,这些方法采用联合分布的参数形式。在本文中,我们定义了一个多维参数,包括毒性和功效结果以及一种,一种或两种都不发生的剂量。根据这两个标准的出现顺序,将每个患者分为有序类别:患者越早从疗效中受益和/或他/她越晚经历毒性,治疗效果就越好。然后,我们将似然比检验与有序替代方案结合使用。此过程需要通过等张回归来约束最大似然估计。大量的仿真将建议的测试与其他更常见的测试进行了比较,结果显示出良好的性能和令人满意的I类错误控制。我们的方法通过一项涉及转移性非精原细胞生殖细胞肿瘤患者的多中心随机临床试验进行了说明。版权所有2003 John Wiley&Sons,Ltd.

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