Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Division of Hematology and Oncology, Vanderbilt University, Nashville, TN, USA.
Br J Haematol. 2019 Sep;186(6):807-819. doi: 10.1111/bjh.16130. Epub 2019 Jul 31.
Treatment response assessment in multiple myeloma (MM) relies on the detection of paraprotein in serum and/or urine, bone marrow morphology and immunohistochemistry. With remarkable advances in therapy, particularly in the newly diagnosed setting, achievement of complete remission became frequent, creating the need to identify smaller amounts of residual disease and understand their prognostic and therapeutic implications. Measurable residual disease (MRD) can be assessed primarily by flow cytometry and next generation sequencing and state-of-the-art assays have sensitivity approaching 1 in 10 cells. This review discusses the existing challenges in utilizing MRD to inform management of MM and highlights open research questions and opportunities as MRD is more routinely incorporated into clinical practice for patients with MM.
在多发性骨髓瘤(MM)中,治疗反应评估依赖于血清和/或尿液中出现单克隆蛋白、骨髓形态学和免疫组织化学的检测。随着治疗的显著进展,尤其是在新诊断的情况下,完全缓解的实现变得更加频繁,这就需要识别更小量的残留疾病,并了解其预后和治疗意义。可测量的残留疾病(MRD)可以主要通过流式细胞术和下一代测序来评估,最先进的检测方法的灵敏度接近每 10 个细胞中有 1 个。这篇综述讨论了利用 MRD 为 MM 患者的管理提供信息所面临的挑战,并强调了作为 MRD 更常规地纳入 MM 患者的临床实践中的开放性研究问题和机会。