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在新型疗法时代,何为高危多发性骨髓瘤?

In the age of novel therapies, what defines high-risk multiple myeloma?

机构信息

University of Maryland, Greenebaum Cancer Center, Bone Marrow Transplant Program, Baltimore, Maryland 21201, USA.

出版信息

J Natl Compr Canc Netw. 2010 Feb;8 Suppl 1:S28-34. doi: 10.6004/jnccn.2010.0114.

Abstract

Multiple myeloma is characterized by clinical and biologic heterogenicity. Recently, genetic analysis has provided predictable prognosis across different types of treatment. These advances have allowed patients to be categorized into different risk groups and have been particularly useful in defining a high-risk group with short survival after standard- and high-dose chemotherapies. Preliminary studies have shown promising outcomes after the use of novel agents, such as bortezomib, thalidomide, and lenalidomide in high-risk patients, including those eligible for autologous stem cell transplantation and those who cannot or will not undergo transplantation. The application of risk-based therapy and the potential of the new agents to abrogate the influence of adverse prognostic features may improve outcomes in these patients.

摘要

多发性骨髓瘤的特征是临床表现和生物学异质性。最近,遗传分析为不同类型的治疗提供了可预测的预后。这些进展使患者能够分为不同的风险组,对于定义标准和高剂量化疗后生存时间短的高危组特别有用。初步研究表明,在高危患者中使用新型药物(如硼替佐米、沙利度胺和来那度胺)后,有较好的结果,包括有资格进行自体干细胞移植的患者和那些不能或不愿进行移植的患者。基于风险的治疗方法的应用和新药物消除不良预后因素的影响的潜力可能会改善这些患者的预后。

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