Ramasamy Karthik, Avet-Loiseau Hervé, Hveding Blimark Cecilie, Delforge Michel, Gay Francesca, Manier Salomon, Martinez-Lopez Joaquín, Mateos Maria Victoria, Mohty Mohamad, van de Donk Niels W C J, Weisel Katja
Oxford University Hospitals NHS Foundation Trust, Radcliffe Department of Medicine, Oxford University, Oxford, United Kingdom.
University Institute of Cancer Toulouse, University Hospital of Toulouse, Toulouse, France.
Hemasphere. 2023 Aug 30;7(9):e942. doi: 10.1097/HS9.0000000000000942. eCollection 2023 Sep.
We used a modified Delphi approach to establish areas of consensus and nonconsensus regarding the utility of determining measurable residual disease (MRD) to assess multiple myeloma (MM) treatment response, which may inform disease management and design of future clinical trials. This modified Delphi study incorporated 2 iterative rounds of surveys to evaluate the opinions of an expert panel of 61 practicing hematological oncologists from across 14 countries in Europe concerning the use of MRD testing in MM management. Survey 1 assessed experts' opinions on MRD testing in different clinical situations and associated challenges. Survey 2 focused on the lack of consensus areas identified in survey 1. Consensus to an individual question was defined as 75% agreement or disagreement by the panel. From the 2 rounds of surveys, the experts reached consensus agreement that MRD testing should be performed in newly diagnosed or relapsed patients who achieved complete response (CR) or better after transplantation. In transplant-ineligible patients, experts recommended MRD testing in those who are ≤70 years old and in CR. If a patient was previously positive on positron-emission tomography and computed tomography (PET/CT), both MRD and PET/CT should be assessed at CR. MRD testing should be performed ≤6 months after transplantation and every 6-12 months in continuously treated patients in CR. There was no consensus on making treatment decisions based on MRD status. MRD testing is an important component of clinical management in MM. Additional data will further clarify the role of MRD in guiding treatment decisions.
我们采用改良的德尔菲法,以确定在评估多发性骨髓瘤(MM)治疗反应时测定可测量残留病(MRD)的效用方面的共识和非共识领域,这可能为疾病管理和未来临床试验的设计提供参考。这项改良的德尔菲研究纳入了两轮迭代调查,以评估来自欧洲14个国家的61名血液肿瘤学执业专家组成的专家小组对在MM管理中使用MRD检测的意见。调查1评估了专家对不同临床情况下MRD检测及其相关挑战的意见。调查2聚焦于调查1中确定的缺乏共识的领域。对单个问题的共识定义为专家小组75%的同意或不同意。通过两轮调查,专家们达成了共识,即对于新诊断或复发且在移植后达到完全缓解(CR)或更好缓解的患者,应进行MRD检测。对于不符合移植条件的患者,专家建议对年龄≤70岁且处于CR的患者进行MRD检测。如果患者先前正电子发射断层扫描和计算机断层扫描(PET/CT)呈阳性,则应在CR时同时评估MRD和PET/CT。MRD检测应在移植后≤6个月进行,对于持续接受治疗且处于CR的患者,应每6 - 12个月进行一次。对于基于MRD状态做出治疗决策,尚未达成共识。MRD检测是MM临床管理的重要组成部分。更多数据将进一步阐明MRD在指导治疗决策中的作用。