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我是如何治疗年轻患者的多发性骨髓瘤。

How I treat multiple myeloma in younger patients.

机构信息

Mayo Clinic Arizona, Scottsdale, Boston, MA, USA.

出版信息

Blood. 2009 Dec 24;114(27):5436-43. doi: 10.1182/blood-2009-07-204651. Epub 2009 Oct 27.

Abstract

Therapeutic options for multiple myeloma (MM) patients have changed quickly in recent years and uncertainty has arisen about optimal approaches to therapy. A reasonable goal of MM treatment in younger "transplant eligible" patients is to initiate therapy with a target goal of durable complete remission, and the anticipated consequence of long-term disease control. [corrected] To achieve this goal we recommend induction therapy with multi-agent combination chemotherapies (usually selected from bortezomib, lenalidomide, thalidomide, cyclophosphamide, and corticosteriods) which when employed together elicit frequent, rapid, and deep responses. We recommend consolidation with high-dose melphalan and autologous stem cell transplantation in the majority of patients willing and able to undergo this procedure and subsequent maintenance therapy in those failing to achieve a complete response or at high risk for early relapse based on prognostic, genetically defined risk factors. Defining genetic risk for early relapse is therefore an important aspect of early diagnostic testing and attention to minimizing expected toxicities once therapy begins is critical in ensuring the efficacy of modern combination therapy approaches. When access to newer drugs is restricted participation in clinical trials should be pursued.

摘要

近年来,多发性骨髓瘤(MM)患者的治疗选择变化迅速,治疗方法的最佳选择也存在不确定性。对于年轻的“适合移植”患者,MM 治疗的合理目标是开始治疗,以持久完全缓解为目标,并期望长期控制疾病。[纠正]为了实现这一目标,我们建议采用多药物联合化疗(通常选自硼替佐米、来那度胺、沙利度胺、环磷酰胺和皮质类固醇)进行诱导治疗,这些药物联合使用可产生频繁、快速和深度的反应。我们建议在大多数愿意和能够接受该手术的患者中进行大剂量美法仑和自体干细胞移植巩固治疗,对于未能达到完全缓解或基于预后、基因定义的危险因素有早期复发高风险的患者进行维持治疗。因此,确定早期复发的遗传风险是早期诊断检测的重要方面,一旦开始治疗,就需要注意最小化预期毒性,这对于确保现代联合治疗方法的疗效至关重要。当获得新药受到限制时,应参加临床试验。

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