Division of Hematology and Oncology, Department of Medicine, O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Section of Hematology/Oncology, University of Chicago Medical Center, Chicago, IL, USA.
Leukemia. 2021 Jan;35(1):18-30. doi: 10.1038/s41375-020-01012-4. Epub 2020 Aug 11.
Minimal residual disease (MRD) assessment is incorporated in an increasing number of multiple myeloma (MM) clinical trials as a correlative analysis, an endpoint or even as a determinant of subsequent therapy. There is substantial heterogeneity across clinical trials in how MRD is assessed and reported, creating challenges for data interpretation and for the design of subsequent studies. We convened an international panel of MM investigators to harmonize how MRD should be assessed and reported in MM clinical trials. The panel provides consensus on which MM trials should include MRD, the recommended time points for MRD assessment, and expected analytical validation for MRD assays. We subsequently outlined parameters for reporting MRD results implementing the intention-to-treat principle. The panel provides guidance regarding the incorporation of newer peripheral blood-based and imaging-based approaches to detection of residual disease. Recommendations are summarized in 13 consensus statements that should be followed by sponsors, investigators, editors, and reviewers engaged in designing, performing, and interpreting MM trials.
微小残留病灶 (MRD) 评估作为相关性分析、终点甚至后续治疗的决定因素,已被纳入越来越多的多发性骨髓瘤 (MM) 临床试验中。在如何评估和报告 MRD 方面,临床试验之间存在着实质性的异质性,这给数据解释和后续研究的设计带来了挑战。我们召集了一个国际多发性骨髓瘤研究人员小组,以协调如何在 MM 临床试验中评估和报告 MRD。该小组就哪些 MM 试验应包括 MRD、MRD 评估的推荐时间点以及 MRD 检测的预期分析验证达成了共识。随后,我们概述了实施意向治疗原则报告 MRD 结果的参数。该小组就纳入新的基于外周血和基于成像的残留疾病检测方法提供了指导。建议总结在 13 条共识声明中,参与设计、进行和解释 MM 试验的赞助商、研究人员、编辑和评审人员应遵循这些声明。