针对复发性 2 级胶质瘤患者的脉冲减剂量率再照射

Colin M Harari, Adam R Burr, Brett A Morris, W. A. Tomé, PhD Adam Bayliss, A. Bhatia, P.T. Grogan, H. I. Robins, S. Howard, WI AveMadison
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2 级胶质瘤患者的存活率差异很大。对复发疾病进行再照射的成熟临床数据有限。我们报告了脉冲降低剂量率(PRDR)放射治疗复发性2级胶质瘤患者的结果。 我们对 2000-2021 年间接受 PRDR 治疗的 58 例患者进行了回顾性分析。放射治疗以每三分钟 0.2 Gy 脉冲的方式进行,照射范围包括肿瘤和边缘。采用卡普兰-梅耶(Kaplan Meier)和考克斯回归分析法对生存率和预后因素进行分析。 自初次手术之日起,中位生存期为 8.6 年(95% CI 5.5-11.8 年)。69%的患者恶变为3级(38%)或4级(31%)胶质瘤。PRDR 后的总生存期为 12.6 个月(95% CI 8.3-17.0 个月),无进展生存期为 6.2 个月(95% CI 3.8-8.6 个月)。根据PRDR后的磁共振成像,总体反应率为36%。在复发时保持 2 级组织学的患者中,PRDR 的总生存期为 22.0 个月,其中 5 名患者保持无病生存,最长的分别为 8.2 年和 11.4 年。PRDR 的耐受性普遍良好。 据我们所知,这是对复发的2级胶质瘤患者采用PRDR放射治疗疾病复发的最大系列报道。我们的研究表明,再次放射治疗后患者的存活率很高,毒性也可接受。在维持 2 级疾病的患者队列中,我们观察到部分患者的生存期延长(>5 年)。在整个队列中,1p19q共缺失、KPS以及从最初诊断到PRDR的时间较长与生存率的提高有关。
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Pulsed Reduced Dose Rate Re-Irradiation for Patients with Recurrent Grade 2 Gliomas
Patients with grade 2 glioma exhibit highly variable survival. Re-irradiation for recurrent disease has limited mature clinical data. We report treatment results of pulsed reduced dose rate (PRDR) radiation for patients with recurrent grade 2 glioma. A retrospective analysis of 58 patients treated with PRDR from 2000-2021 was performed. Radiation was delivered in 0.2 Gy pulses every three minutes encompassing tumor plus margin. Survival outcomes and prognostic factors on outcome were Kaplan Meier and Cox regression analyses. The median survival from date of initial surgery was 8.6 years (95% CI 5.5-11.8 yrs). 69% of patients showed malignant transformation to grade 3 (38%) or grade 4 (31%) glioma. Overall survival following PRDR was 12.6 months (95% CI 8.3-17.0 mo) and progression free survival was 6.2 months (95% CI 3.8-8.6 mo). Overall response rate based on post PRDR MRI was 36%. In patients who maintained grade 2 histology at recurrence, overall survival from PRDR was 22.0 months with five patients remaining disease free, the longest at 8.2 and 11.4 years. PRDR was generally well tolerated. To our knowledge, this is the largest reported series of patients with recurrent grade 2 gliomas treated with PRDR radiation for disease recurrence. We demonstrate promising survival and acceptable toxicity profiles following re-irradiation. In the cohort of patients who maintain grade 2 disease, prolonged survival (>5 years) is observed in selected patients. For the entire cohort, 1p19q co-deletion, KPS, and longer time from initial diagnosis to PRDR were associated with improved survival.
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