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全脑放疗联合美金刚治疗脑转移瘤患者时对海马的回避:NRG 肿瘤学 CC001 期临床试验。

Hippocampal Avoidance During Whole-Brain Radiotherapy Plus Memantine for Patients With Brain Metastases: Phase III Trial NRG Oncology CC001.

机构信息

Mayo Clinic, Rochester, MN.

Northwestern Medicine Cancer Center Warrenville and Northwestern Medicine Proton Center, Warrenville, IL.

出版信息

J Clin Oncol. 2020 Apr 1;38(10):1019-1029. doi: 10.1200/JCO.19.02767. Epub 2020 Feb 14.

Abstract

PURPOSE

Radiation dose to the neuroregenerative zone of the hippocampus has been found to be associated with cognitive toxicity. Hippocampal avoidance (HA) using intensity-modulated radiotherapy during whole-brain radiotherapy (WBRT) is hypothesized to preserve cognition.

METHODS

This phase III trial enrolled adult patients with brain metastases to HA-WBRT plus memantine or WBRT plus memantine. The primary end point was time to cognitive function failure, defined as decline using the reliable change index on at least one of the cognitive tests. Secondary end points included overall survival (OS), intracranial progression-free survival (PFS), toxicity, and patient-reported symptom burden.

RESULTS

Between July 2015 and March 2018, 518 patients were randomly assigned. Median follow-up for alive patients was 7.9 months. Risk of cognitive failure was significantly lower after HA-WBRT plus memantine versus WBRT plus memantine (adjusted hazard ratio, 0.74; 95% CI, 0.58 to 0.95; = .02). This difference was attributable to less deterioration in executive function at 4 months (23.3% 40.4%; = .01) and learning and memory at 6 months (11.5% 24.7% [ = .049] and 16.4% 33.3% [ = .02], respectively). Treatment arms did not differ significantly in OS, intracranial PFS, or toxicity. At 6 months, using all data, patients who received HA-WBRT plus memantine reported less fatigue ( = .04), less difficulty with remembering things ( = .01), and less difficulty with speaking ( = .049) and using imputed data, less interference of neurologic symptoms in daily activities ( = .008) and fewer cognitive symptoms ( = .01).

CONCLUSION

HA-WBRT plus memantine better preserves cognitive function and patient-reported symptoms, with no difference in intracranial PFS and OS, and should be considered a standard of care for patients with good performance status who plan to receive WBRT for brain metastases with no metastases in the HA region.

摘要

目的

研究发现,海马神经再生区的辐射剂量与认知毒性有关。全脑放疗(WBRT)期间使用强度调制放疗进行海马回避(HA),据推测可以保留认知功能。

方法

这项 III 期试验招募了患有脑转移的成年患者,将其随机分为 HA-WBRT 加美金刚或 WBRT 加美金刚。主要终点是认知功能衰竭的时间,定义为至少一项认知测试中使用可靠变化指数下降。次要终点包括总生存期(OS)、颅内无进展生存期(PFS)、毒性和患者报告的症状负担。

结果

2015 年 7 月至 2018 年 3 月期间,共 518 例患者被随机分配。对存活患者的中位随访时间为 7.9 个月。HA-WBRT 加美金刚组的认知失败风险明显低于 WBRT 加美金刚组(调整后的危险比为 0.74;95%CI,0.58 至 0.95;P=0.02)。这一差异归因于在 4 个月时执行功能的恶化程度较低(23.3% vs. 40.4%;P=0.01)和在 6 个月时学习和记忆能力的恶化程度较低(11.5% vs. 24.7%[P=0.049]和 16.4% vs. 33.3%[P=0.02])。OS、颅内 PFS 或毒性在治疗组之间没有显著差异。在 6 个月时,使用所有数据,接受 HA-WBRT 加美金刚治疗的患者报告疲劳程度更低(P=0.04)、记忆困难程度更低(P=0.01)、言语困难程度更低(P=0.049),并且使用推断数据,神经系统症状对日常生活的干扰程度更低(P=0.008)和认知症状更少(P=0.01)。

结论

HA-WBRT 加美金刚能更好地保留认知功能和患者报告的症状,颅内 PFS 和 OS 无差异,对于计划接受 WBRT 治疗无 HA 区转移的脑转移且一般状况良好的患者,应考虑作为标准治疗。

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