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微小残留病灶指导下的多发性骨髓瘤治疗:现有证据和观点。

Minimal Residual Disease-Adapted Therapy in Multiple Myeloma: Current Evidence and Opinions.

机构信息

Myeloma Institute, Sylvester Comprehensive Cancer Center, University of Miami, 1120 NW 14th Street, Clinical Research Building, Miami, FL, 33136, USA.

出版信息

Curr Oncol Rep. 2024 Jun;26(6):679-690. doi: 10.1007/s11912-024-01537-2. Epub 2024 Apr 27.

Abstract

PURPOSE OF REVIEW

Multiple myeloma (MM) is a biologically heterogeneous malignancy with relatively uniform treatment paradigms. This review aims to assess the growing role of Minimal Residual Disease (MRD) assessment in facilitating response-adapted therapeutic decision making to individualize therapy in MM.

RECENT FINDINGS

MRD has been repeatedly demonstrated to provide strong prognostic information, superseding traditional IMWG response criteria. The use of MRD to modulate therapy remains controversial. Here, we review the existing landscape of MRD-adapted trial designs in both induction/consolidation and maintenance settings, including recent data from influential studies and retrospective analyses. We navigate existing data, leverage the increased resolution of longitudinal MRD assessments, and comment on trials in progress to explain our current utilization of MRD in the clinic. MRD transcends traditional response assessments by providing a window into disease-treatment interaction over time. As a strong patient-level surrogate, MRD has limited current use in individualizing treatment, but is poised to comprehensively shape treatment strategies at many key points in a patient's MM course.

摘要

目的综述

多发性骨髓瘤(MM)是一种生物学异质性恶性肿瘤,具有相对统一的治疗模式。本综述旨在评估微小残留病(MRD)评估在促进适应反应的治疗决策中的作用,以实现 MM 治疗的个体化。

最近的发现

MRD 已被反复证明提供了强大的预后信息,超越了传统的 IMWG 反应标准。使用 MRD 来调节治疗仍然存在争议。在这里,我们回顾了诱导/巩固和维持治疗中现有的基于 MRD 的试验设计,包括来自有影响力的研究和回顾性分析的最新数据。我们探讨了现有数据,利用纵向 MRD 评估的提高分辨率,并对正在进行的试验进行评论,以解释我们目前在临床上对 MRD 的应用。MRD 通过提供随时间推移的疾病-治疗相互作用的窗口,超越了传统的反应评估。作为一个强有力的患者水平替代指标,MRD 在个体化治疗中的应用有限,但有望在患者 MM 病程的许多关键点上全面塑造治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/11169024/f4ea31c7f360/11912_2024_1537_Fig1_HTML.jpg

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