Department of Surgery, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
Department of Radiation Oncology, BC Cancer - Vancouver, 600 West 10th Ave, Vancouver, BC, V5Z 4E6, Canada.
Radiat Oncol. 2020 Nov 25;15(1):271. doi: 10.1186/s13014-020-01717-x.
To investigate predictors of cognitive decline after whole brain radiotherapy (WBRT) for brain metastases.
A secondary analysis of a phase 2 clinical trial was conducted in patients who received stereotactic radiosurgery for 1-10 brain metastases and WBRT (NCT01046123). The Montreal Cognitive Assessment (MoCA) was performed at baseline and every 3 months after WBRT. Baseline T2-weighted fluid attenuation inversion recovery magnetic resonance imaging was independently assessed by two neuroradiologists for the presence of white matter hyperintensities (WMH) using the Fazekas visual rating scale. WMH were also manually segmented for volumetric analysis. Univariable and multivariable logistic regression were used to test the association between baseline variables and MoCA score decline.
Forty-six patients survived ≥ 3 months after treatment. Age (OR 1.12 (1.04-1.21), p < 0.01), baseline WMH volume (OR 1.20, 95% CI 1.06-1.52, p = 0.02) and baseline Fazekas score ≥ 3/6 (OR 6.4, 95% CI 1.7-24.7, p < 0.01) were predictive of MoCA score decline. In multivariable analysis, age was the only significant predictor of MoCA decline. However, all three patients with pre-treatment leukoencephalopathy (Fazekas score = 6/6) had notable adverse outcomes due to cognitive impairment: one required full-time home nursing support and two were institutionalized.
A greater decline in cognition after WBRT was observed in older patients and patients with a higher baseline WMH burden. Although this study is small and hypothesis-generating, we propose that radiation oncologists should exercise caution in prescribing WBRT if leukoencephalopathy is present on pre-treatment imaging.
clinicaltrials.gov identifier NCT01046123. First posted January 11, 2010. https://clinicaltrials.gov/ct2/show/NCT01046123.
研究全脑放疗(WBRT)治疗脑转移瘤后认知能力下降的预测因素。
对接受立体定向放射外科治疗 1-10 个脑转移瘤和 WBRT 的患者(NCT01046123)进行了一项 2 期临床试验的二次分析。在 WBRT 后,使用蒙特利尔认知评估(MoCA)在基线和每 3 个月进行一次评估。使用 Fazekas 视觉评分量表,由两位神经放射科医生独立评估基线 T2 加权液体衰减反转恢复磁共振成像,以评估是否存在脑白质高信号(WMH)。还手动分割 WMH 进行容积分析。使用单变量和多变量逻辑回归来测试基线变量与 MoCA 评分下降之间的关联。
46 例患者在治疗后生存时间≥3 个月。年龄(OR 1.12(1.04-1.21),p<0.01)、基线 WMH 体积(OR 1.20,95%CI 1.06-1.52,p=0.02)和基线 Fazekas 评分≥3/6(OR 6.4,95%CI 1.7-24.7,p<0.01)是 MoCA 评分下降的预测因素。多变量分析中,年龄是 MoCA 下降的唯一显著预测因素。然而,所有 3 例有治疗前白质脑病(Fazekas 评分=6/6)的患者因认知障碍而出现明显不良后果:1 例需要全职家庭护理支持,2 例被收容。
在 WBRT 后,年龄较大的患者和基线 WMH 负担较高的患者认知能力下降更为明显。尽管这项研究规模较小,且仅是初步研究结果,但我们建议,如果在治疗前的影像学检查中存在白质脑病,放射肿瘤学家在开具 WBRT 处方时应谨慎。
clinicaltrials.gov 标识符 NCT01046123。首次发布于 2010 年 1 月 11 日。https://clinicaltrials.gov/ct2/show/NCT01046123。