首页> 外文期刊>Hematological oncology >Emergence of central nervous system myeloma in the era of novel agents
【24h】

Emergence of central nervous system myeloma in the era of novel agents

机译:新药时代中枢神经系统骨髓瘤的出现

获取原文
获取原文并翻译 | 示例
       

摘要

Although multiple myeloma (MM) remains an incurable disease, considerable improvements in survival have been made with the introduction of autologous stem cell transplantation and new drugs. Central nervous system (CNS) MM is a rare complication associated with poor survival. Historically, CNS disease developed early in the course of MM; however recently, patients often present with CNS disease following multiple lines of therapy. It is hypothesized that exposure to novel agents (thalidomide, lenalidomide and bortezomib) changes the natural history of MM, increasing the lifetime risk of CNS disease. We analysed the baseline characteristics, treatment and outcome data of patients who presented with CNS MM at Peter MacCallum Cancer Centre between 2001 and 2010. Seven patients were identified, from 2005 onwards. All patients were Durie-Salmon stage IIIA or IIIB and International Staging System Scores I to III at baseline. All had received at least three lines of therapy, including high-dose chemotherapy with autologous stem cell transplantation and a novel agent, prior to developing CNS MM. Median time from diagnosis to CNS disease was 24months (range 10-42). All patients died after developing CNS disease with median survival post-CNS disease of 2months (range 1-23). The incidence of CNS MM is increasing, and time to development of CNS manifestations is prolonging, associated with increased use of high-dose chemotherapy and novel agents. Whether this is due to improved overall survival or specific characteristics of these therapies is not clear. Despite the availability of novel agents, survival after CNS MM remains poor.
机译:尽管多发性骨髓瘤(MM)仍然是无法治愈的疾病,但自体干细胞移植和新药的引入已使存活率有了显着提高。中枢神经系统(CNS)MM是与生存不良相关的罕见并发症。从历史上看,中枢神经系统疾病是在MM病程早期发展的。然而,最近,患者经常在接受多种疗法后出现中枢神经系统疾病。假设接触新型药物(沙利度胺,来那度胺和硼替佐米)会改变MM的自然病史,增加中枢神经系统疾病的终生风险。我们分析了2001年至2010年在Peter MacCallum癌症中心接受CNS MM治疗的患者的基线特征,治疗和结局数据。从2005年开始,确定了7例患者。所有患者在基线时均为Durie-Salmon IIIA或IIIB期,国际分期系统评分I至III。在发展中枢神经系统MM之前,所有人都至少接受了三线治疗,包括大剂量化疗加自体干细胞移植和新型药物。从诊断到中枢神经系统疾病的中位时间为24个月(范围10-42)。所有患者均在发展为中枢神经系统疾病后死亡,中枢神经系统疾病后中位生存期为2个月(范围1-23)。中枢神经系统MM的发生率正在增加,中枢神经系统表现的发展时间延长,这与大剂量化学疗法和新型药物的使用增加有关。目前尚不清楚这是由于总体生存率的提高还是这些疗法的特定特征所致。尽管可以使用新型药物,但CNS MM术后的生存仍然很差。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号