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我们应该如何治疗新诊断的多发性骨髓瘤患者?

How should we treat newly diagnosed multiple myeloma patients?

作者信息

Mateos María-Victoria, San Miguel Jesús F

机构信息

1Hospital Universitario de Salamanca and.

出版信息

Hematology Am Soc Hematol Educ Program. 2013;2013:488-95. doi: 10.1182/asheducation-2013.1.488.

DOI:10.1182/asheducation-2013.1.488
PMID:24319223
Abstract

Multiple myeloma (MM) is the second most frequent hematological disease. Two-thirds of newly diagnosed MM patients are more than 65 years of age. Elsewhere in this issue, McCarthy et al discuss the treatment of transplantation candidates; this chapter focuses on the data available concerning therapy for non-transplantation-eligible MM patients. Treatment goals for these non-transplantation-eligible patients should be to prolong survival by achieving the best possible response while ensuring quality of life. Until recently, treatment options were limited to alkylators, but new up-front treatment combinations based on novel agents (proteasome inhibitors and immunomodulatory drugs) plus alkylating agents have significantly improved outcomes. Other nonalkylator induction regimens are also available and provide a novel backbone that may be combined with novel second- and third-generation drugs. Phase 3 data indicate that maintenance therapy or prolonged treatment in elderly patients also improves the quality and duration of clinical responses, extending time to progression and progression-free survival; however, the optimal scheme, appropriate doses, and duration of long-term therapy have not yet been fully determined. The potential for novel treatment regimens to improve the adverse prognosis associated with high-risk cytogenetic profiles also requires further research. In summary, although we have probably doubled the survival of elderly patients, this group requires close monitoring and individualized, dose-modified regimens to improve tolerability and treatment efficacy while maintaining their quality of life.

摘要

多发性骨髓瘤(MM)是第二常见的血液系统疾病。三分之二新诊断的MM患者年龄超过65岁。在本期的其他地方,麦卡锡等人讨论了适合移植患者的治疗;本章重点关注关于不适合移植的MM患者治疗的现有数据。这些不适合移植患者的治疗目标应该是通过实现尽可能好的缓解来延长生存期,同时确保生活质量。直到最近,治疗选择还仅限于烷化剂,但基于新型药物(蛋白酶体抑制剂和免疫调节药物)加烷化剂的新的一线治疗组合显著改善了治疗结果。其他非烷化剂诱导方案也可用,并提供了一种可与新型第二代和第三代药物联合的新框架。3期数据表明,老年患者的维持治疗或延长治疗也可改善临床缓解的质量和持续时间,延长至疾病进展时间和无进展生存期;然而,长期治疗的最佳方案、合适剂量和持续时间尚未完全确定。新型治疗方案改善与高危细胞遗传学特征相关的不良预后的潜力也需要进一步研究。总之,尽管我们可能使老年患者的生存期延长了一倍,但这组患者需要密切监测和个体化、调整剂量的方案,以提高耐受性和治疗效果,同时维持他们的生活质量。

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