高剂量RE辐射用于THOrax (RETHO) 中的现场复发性肺癌:第二阶段前性临床试验的结果
E Cammareri1, M Duijm2, P V Granton2
1Department of Radiation Oncology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands; Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
International journal of radiation oncology, biology, physics
|December 22, 2025
概括
高剂量胸部再辐射有效治疗复发性肺癌,显著改善整体存活率和局部控制,可控毒性. 这种方法为在初始治疗后复发具有挑战性的患者提供了一个有前途的选择.
科学领域:
- 在瘤学瘤学.
- 辐射瘤学 辐射瘤学
- 临床试验 临床试验
背景情况:
- 地方区域性失效发生在30%的初级肺癌病例中,这些病例发生在化疗后的放射治疗后.
- 对肺癌复发的再辐射具有重大临床挑战.
- 一项前性第二阶段试验评估了对边缘性或现场肺癌复发的胸部再辐射.
研究的目的:
- 评估高剂量胸部再辐射治疗复发性肺癌的疗效和安全性.
- 在患有复发性肺癌的患者中,实现12个月的平均整体存活期 (OS).
- 评估二级终点,包括局部控制 (LC),无病生存率 (DFS) 和毒性.
主要方法:
- 前性第二阶段试验,涉及患有复发性肺癌的患者,距离之前的50Gy10 EQD2同位素剂量线5厘米之内.
- 使用图像导向强度调制辐射疗法 (IMRT) 或体积调制弧线疗法 (VMAT) 进行的再辐射,剂量≥45Gy10 EQD2.
- 患者接受了常规分成型放射治疗或立体性身体辐射治疗 (SBRT).
主要成果:
- 平均生存期为30.1个月,明显超过了12个月的目标.
- 中位数局部控制 (LC) 为28.2个月,中位数无病生存 (DFS) 为13.6个月.
- 3级毒性发生在20%的患者中,主要是肺炎;没有观察到4-5级毒性.
结论:
- 高剂量的胸部再辐射是复发性肺癌的有效治疗方法.
- 该研究取得了有利的整体存活率,局部控制和无病存活率.
- 再辐射显示出有利的毒性概况,使其成为选定的患者的可行选择.
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