...
首页> 外文期刊>Journal of oncology pharmacy practice: official publication of the International Society of Oncology Pharmacy Practitioners >Corticosteroids for the management of immune-related adverse events in patients receiving checkpoint inhibitors
【24h】

Corticosteroids for the management of immune-related adverse events in patients receiving checkpoint inhibitors

机译:用于治疗接受检查点抑制剂的患者免疫相关不良事件的皮质类固醇

获取原文
获取原文并翻译 | 示例
           

摘要

Introduction Due to enhanced T-cell activity, immune checkpoint inhibitors cause immune-related adverse effects. Corticosteroids are the mainstay of immune-related adverse effect management but the optimal strategy has not been determined, putting patients at risk for steroid-related adverse effects and potentially decreased efficacy of immunotherapy. This study aims to characterize the use of corticosteroids for the management of immune-related adverse effect. Methods and materials A retrospective, single-center evaluation of patients receiving checkpoint inhibitors was conducted. The primary objective was to evaluate corticosteroid use for immune-related adverse effects, including starting dose, taper strategy, total duration, and resumption of immunotherapy. Secondary objective was to describe the incidence and significance of hyperglycemia. Results One hundred and three patients met inclusion criteria and experienced 123 immune-related adverse effects. Prednisone was used most commonly (67%) at an average starting dose of 0.88?mg/kg (range 0.07–17.0). On average, steroid tapers began 9.2 days after initiation (range 0–89) and were continued for a total of 84.2 days (range 3–693). In 21.1% of cases, checkpoint inhibitor therapy was not delayed and 68.6% resumed checkpoint inhibitors, while the patient was taking steroids (30.4?mg prednisone on average, range 5–80). On average, checkpoint inhibitor therapy was resumed 18.6 days after detection of immune-related adverse effect (range 0–150). Clinically relevant hyperglycemia occurred in 8.9%. Conclusion Utilization of steroids for immune-related adverse effect at our institution is highly variable. The majority of patients received prolonged courses of steroids and resumed checkpoint inhibitor therapy with concomitant steroids above recommended doses. Additional monitoring for hyperglycemia and other steroid associated adverse effects should be considered.
机译:由于增强的T细胞活性引入,免疫检查点抑制剂导致免疫相关的不良反应。皮质类固醇是免疫相关的不良反垄断管理的主要影响,但尚未确定最佳策略,使患者患者对类固醇相关的不良影响的风险,并可能降低免疫疗法的疗效。本研究旨在表征皮质类固醇对免疫相关不良影响的管理。方法和材料对接受检查点抑制剂的患者进行回顾性,单中心评估。主要目标是评估皮质类固醇用于免疫相关的不良反应,包括开始剂量,锥度策略,总持续时间和免疫疗法的恢复。次要目标是描述高血糖的发病率和意义。结果百年和三名患者符合纳入标准,经历了123例免疫相关不良反应。泼尼松最常使用(67%),平均起始剂量为0.88Ωmg/ kg(范围0.07-17.0)。平均而言,服饰锥度开始于发起(0-89档)后9.2天,共持续84.2天(范围3-693)。在21.1%的病例中,检查点抑制剂治疗未延迟,恢复68.6%的检查点抑制剂,而患者服用类固醇(平均平均值为5-80次,范围为5-80)。平均而言,在检测免疫相关不良反应(范围0-150)后,检查点抑制剂治疗18.6天。临床相关的高血糖发生在8.9%。结论在我们机构的免疫相关不良影响的使用类固醇是高度可变的。大多数患者接受了延长的类固醇疗程,并随后用伴随的类固醇恢复检查点抑制剂治疗。应考虑对高血糖和其他类固醇相关不利影响的额外监测。

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