医学
微小残留病
危险系数
内科学
临床试验
肿瘤科
疾病
荟萃分析
置信区间
儿科
梅德林
白血病
政治学
法学
作者
Donald A. Berry,Shouhao Zhou,Howard R. Higley,Lata Mukundan,Shuangshuang Fu,Gregory H. Reaman,Brent L. Wood,Gary J. Kelloff,J. Milburn Jessup,Jerald P. Radich
出处
期刊:JAMA Oncology
[American Medical Association]
日期:2017-05-11
卷期号:3 (7): e170580-e170580
被引量:529
标识
DOI:10.1001/jamaoncol.2017.0580
摘要
The value of having achieved MRD negativity is substantial in both pediatric and adult patients with ALL. These results are consistent across therapies, methods of and times of MRD assessment, cutoff levels, and disease subtypes. Minimal residual disease status warrants consideration as an early measure of disease response for evaluating new therapies, improving the efficiency of clinical trials, accelerating drug development, and for regulatory approval. A caveat is that an accelerated approval of a particular new drug using an intermediate end point, such as MRD, would require confirmation using traditional efficacy end points.
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