首页> 美国卫生研究院文献>Mayo Clinic Proceedings >Induction of a Chronic Disease State in Patients With Smoldering or Indolent Multiple Myeloma by Targeting Interleukin 1β-Induced Interleukin 6 Production and the Myeloma Proliferative Component
【2h】

Induction of a Chronic Disease State in Patients With Smoldering or Indolent Multiple Myeloma by Targeting Interleukin 1β-Induced Interleukin 6 Production and the Myeloma Proliferative Component

机译:靶向白细胞介素1β诱导的白细胞介素6产生和骨髓瘤增殖成分诱导的闷烧或惰性多发性骨髓瘤患者的慢性疾病状态的诱导

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

OBJECTIVE: To conduct in vitro studies as well as a phase 2 clinical trial in patients with smoldering or indolent multiple myeloma to determine if interleukin 1 (IL-1) inhibitors can delay or prevent active myeloma.PATIENTS AND METHODS: Stromal cells were cocultured with IL-1β-expressing myeloma cells in the presence of dexamethasone, IL-1 receptor antagonist (IL-1Ra), or both. Levels of interleukin 6 (IL-6) and of apoptosis were also quantified. Between November 19, 2002, and May 24, 2007, 47 patients were enrolled in the study and subsequently treated with IL-1Ra. In 25 (53%) of the 47 study patients, low-dose dexamethasone (20 mg/wk) was added. The primary end point was progression-free survival (PFS).RESULTS: In vitro, IL-1Ra was superior to dexamethasone at inhibiting IL-6 production; maximal IL-6 inhibition and apoptosis induction were achieved by addition of both IL-1Ra and dexamethasone. In the clinical trial, 3 patients achieved a minor response to IL-1Ra alone; 5 patients achieved a partial response and 4 patients a minor response after addition of dexamethasone. Seven patients showed a decrease in the plasma cell labeling index that paralleled a decrease in high-sensitivity C-reactive protein (hs-CRP) levels. The median overall PFS was 37.5 months. The median PFS for patients without (n=12) or with (n=35) a greater than 15% decrease in 6-month vs baseline hs-CRP levels was 6 months and more than 3 years, respectively (P=.002). Disease stability was maintained in 8 patients who received therapy for more than 4 years.CONCLUSION: In patients with smoldering or indolent multiple myeloma who were at risk of progression to active myeloma, treatment with IL-1 inhibitors decreased the myeloma proliferative rate and hs-CRP levels in those who responded, leading to a chronic disease state and an improved PFS.Trial Registration: clinicaltrials.gov identifier:
机译:目的:对闷烧或惰性的多发性骨髓瘤患者进行体外研究以及2期临床试验,以确定白介素1(IL-1)抑制剂是否可以延迟或预防活动性骨髓瘤。患者与方法:将基质细胞与在地塞米松,IL-1受体拮抗剂(IL-1Ra)或两者同时存在的情况下,表达IL-1β的骨髓瘤细胞。白细胞介素6(IL-6)和细胞凋亡的水平也被量化。在2002年11月19日至2007年5月24日之间,共有47位患者参加了研究,随后接受IL-1Ra治疗。在47位研究患者中,有25位(53%)加入了小剂量地塞米松(20 mg / wk)。结果:在体外,IL-1Ra在抑制IL-6产生方面优于地塞米松;在体外,IL-1Ra优于地塞米松。通过同时添加IL-1Ra和地塞米松可以达到最大的IL-6抑制和凋亡诱导。在临床试验中,有3例患者仅对IL-1Ra产生了轻微反应;其余3例仅对IL-1Ra有轻微反应。添加地塞米松后有5例患者出现部分缓解,有4例患者出现轻微缓解。 7名患者的浆细胞标记指数下降,与高敏C反应蛋白(hs-CRP)水平下降同时出现。 PFS的中位数为37.5个月。与基线hs-CRP水平相比,没有(n = 12)或具有(n = 35)的患者在6个月内的基线PFS分别下降了15%以上和3年以上(P = .002) 。 8例接受了4年以上治疗的患者保持了疾病稳定性。结论:在患有闷热或惰性的多发性骨髓瘤患者中,他们有发展为活动性骨髓瘤的风险,使用IL-1抑制剂治疗可降低骨髓瘤的增殖率和hs-有反应者中的CRP水平导致慢性疾病状态和PFS改善。试验注册:clinicaltrials.gov标识符:

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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