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不良事件负担评分——癌症临床试验的一种通用汇总指标

Adverse Event Burden Score-A Versatile Summary Measure for Cancer Clinical Trials.

作者信息

Le-Rademacher Jennifer G, Hillman Shauna, Storrick Elizabeth, Mahoney Michelle R, Thall Peter F, Jatoi Aminah, Mandrekar Sumithra J

机构信息

Department of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.

IQVIA, Raleigh-Durham, NC 27703, USA.

出版信息

Cancers (Basel). 2020 Nov 4;12(11):3251. doi: 10.3390/cancers12113251.

Abstract

This article introduces the adverse event (AE) burden score. The AE burden by treatment cycle is a weighted sum of all grades and AEs that the patient experienced in a cycle. The overall AE burden score is the total AE burden the patient experienced across all treatment cycles. AE data from two completed Alliance multi-center randomized double-blind placebo-controlled trials, with different AE profiles (NCCTG 97-24-51: 176 patients, and A091105: 83 patients), were utilized for illustration. Results of the AE burden score analyses corroborated the trials' primary results. In 97-24-51, the overall AE burden for patients on the treatment arm was 2.2 points higher than those on the placebo arm, with a higher AE burden for patients who went off treatment early due to AE. Similarly, in A091105, the overall AE burden was 1.6 points higher on the treatment arm. On the placebo arms, the AE burden in 97-24-51 remained constant over time; and increased in later cycles in A091105, likely attributable to the increase in disease morbidity. The AE burden score enables statistical comparisons analogous to other quantitative endpoints in clinical trials, and can readily accommodate different trial settings, diseases, and treatments, with diverse AE profiles.

摘要

本文介绍了不良事件(AE)负担评分。按治疗周期计算的AE负担是患者在一个周期内经历的所有等级AE的加权总和。总体AE负担评分是患者在所有治疗周期中经历的总AE负担。为了进行说明,使用了两项已完成的联盟多中心随机双盲安慰剂对照试验的AE数据,这两项试验具有不同的AE特征(NCCTG 97 - 24 - 51:176例患者,A091105:83例患者)。AE负担评分分析结果证实了试验的主要结果。在97 - 24 - 51试验中,治疗组患者的总体AE负担比安慰剂组高2.2分,因AE提前停止治疗的患者AE负担更高。同样,在A091105试验中,治疗组的总体AE负担高1.6分。在安慰剂组中,97 - 24 - 51试验中的AE负担随时间保持不变;而在A091105试验中,后期周期的AE负担增加,这可能归因于疾病发病率的增加。AE负担评分能够进行类似于临床试验中其他定量终点的统计比较,并且可以轻松适应不同的试验设置、疾病和治疗方法,以及具有不同AE特征的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdb/7694214/2d4f01caeccd/cancers-12-03251-g001.jpg

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