Division of Hematology, Mayo Clinic, Rochester, MN, USA.
Blood Cancer J. 2020 Sep 28;10(9):94. doi: 10.1038/s41408-020-00359-2.
The treatment of multiple myeloma (MM) continues to evolve rapidly with arrival of multiple new drugs, and emerging data from randomized trials to guide therapy. Along the disease course, the choice of specific therapy is affected by many variables including age, performance status, comorbidities, and eligibility for stem cell transplantation. In addition, another key variable that affects treatment strategy is risk stratification of patients into standard and high-risk MM. High-risk MM is defined by the presence of t(4;14), t(14;16), t(14;20), gain 1q, del(17p), or p53 mutation. In this paper, we provide algorithms for the treatment of newly diagnosed and relapsed MM based on the best available evidence. We have relied on data from randomized controlled trials whenever possible, and when appropriate trials to guide therapy are not available, our recommendations reflect best practices based on non-randomized data, and expert opinion. Each algorithm has been designed to facilitate easy decision-making for practicing clinicians. In all patients, clinical trials should be considered first, prior to resorting to the standard of care algorithms we outline.
多发性骨髓瘤(MM)的治疗随着多种新药的出现和随机试验的新数据不断快速发展,以指导治疗。在疾病过程中,特定治疗方法的选择受到许多因素的影响,包括年龄、体能状态、合并症和干细胞移植的资格。此外,另一个影响治疗策略的关键变量是将患者分层为标准风险和高风险 MM。高风险 MM 定义为存在 t(4;14)、t(14;16)、t(14;20)、1q 增益、del(17p)或 p53 突变。在本文中,我们根据现有最佳证据提供了新诊断和复发性 MM 的治疗算法。只要有可能,我们就依赖于随机对照试验的数据,当没有合适的试验来指导治疗时,我们的建议反映了基于非随机数据和专家意见的最佳实践。每个算法的设计都旨在方便临床医生做出决策。在所有患者中,应首先考虑临床试验,然后再采用我们概述的标准治疗算法。