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Combined high dose radiation and pazopanib in metastatic renal cell carcinoma: a phase I dose escalation trial

机译:联合高剂量辐射和帕唑帕尼治疗转移性肾细胞癌:I期剂量递增试验

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摘要

Background: The primary objective was to determine maximum tolerated radiation dose in patients with metastatic renal cell carcinoma on pazopanib treatment. Methods: Treatment-naive patients received pazopanib according to standard of care. Stereotactic body radiotherapy (SBRT) was delivered concurrently to the largest metastatic lesion at day 8, 10 and 12. SBRT doses were escalated in 3 dose levels (24 Gy/3, 30 Gy/3 and 36 Gy/3). Dose level was assigned using Time-to-Event Continual Reassessment Method with the target dose-limiting toxicity rate set to 0.25. Results: Thirteen patients were included. One patient experienced dose limiting toxicity (DLT) at dose level 3 (grade 4 hypoglycemia). Maximum tolerated dose was not reached with a recommended dose of 36 Gy/3 having a probability of DLT of 11%. One-year local control was 83% (95% confidence interval 61-100) and 1-year progression-free survival was 28% (95% confidence interval 1-55). Conclusions: SBRT in combination with pazopanib is well tolerated with good local control and response rates outside the radiation field. Trial registration: This trial was retrospectively registered on clinicaltrials. gov(NCT02334709) on January 6th, 2015.
机译:背景:主要目的是确定接受帕唑帕尼治疗的转移性肾细胞癌患者的最大耐受放射剂量。方法:未接受过治疗的患者根据护理标准接受帕唑帕尼治疗。立体定向放射疗法(SBRT)在第8、10和12天同时递送至最大的转移灶。SBRT剂量按3个剂量水平(24 Gy / 3、30 Gy / 3和36 Gy / 3)逐步增加。使用事件持续时间重新评估方法分配剂量水平,并将目标剂量限制毒性率设为0.25。结果:共纳入13例患者。一名患者在剂量水平3(4级低血糖)下经历了剂量限制性毒性(DLT)。使用36 Gy / 3的推荐剂量(DLT的可能性为11%)未达到最大耐受剂量。一年局部控制率为83%(95%置信区间61-100),一年无进展生存期为28%(95%置信区间1-55)。结论:SBRT与帕唑帕尼联合使用具有良好的耐受性,在辐射场外具有良好的局部控制和响应率。试验注册:该试验在临床试验中进行回顾性注册。 gov(NCT02334709)于2015年1月6日发布。

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