RADIOSURGICAL TREATMENT OF RECURRENT GLIOBLASTOMA AND PROGNOSTIC FACTORS AFFECTING TREATMENT OUTCOMES.

Q3 Medicine
O Ya Glavatskyi, A B Griazov, O Yu Chuvashova, I V Kruchok, A A Griazov, H V Khmelnytskyi, I M Shuba, V A Stuley, O V Zemskova
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引用次数: 0

Abstract

Background: Glioblastoma (GBM) is the most prevalent malignant tumor of the brain in adults with the inherent aggressive behavior and high recurrence rate. The stereotactic radiosurgery (SRS) is currently considered as one of the effective modalities for GBM treatment allowing for the improvement of survival with the acceptable toxicity level.

Aim: To assess the effects of various factors on the survival of GBM patients following SRS.

Patients and methods: We retrospectively reviewed treatment outcomes of 68 patients who received SRS for recurrent GBM treatment in 2014-2020. SRS was delivered with Trilogy linear accelerator (6 MeV). The area of recurrent tumor/continued tumor growth was irradiated. For the treatment of the primary GBM, the adjuvant radiotherapy was provided at the standard fractionated regimen with the total boost dose of 60 Gy divided to 30 fractions (Stupp's protocol) in the setting of the concomitant chemotherapy with temozolomide. 36 patients then received temozolomide as the maintenance chemotherapy. SRS for the treatment of recurrent GBM was provided at a boost dose of 20.2 Gy on average being delivered into 1-5 fractions with average single dose of 12.4 Gy. The survival was analyzed by the Kaplan-Meier method with a log-rank test used for assessing the impact of the independent predictors on the survival risks.

Results: The median overall survival (OS) was 21.7 months (95% confidence interval (CІ) 16.4-43.1), median survival after SRS was 9.3 months (95% CІ 5.6-22.7). The majority of patients (72%) were alive for at least 6 months following SRS and about half of patients (48%) survived for at least 24 months following the resection of the primary tumor. OS and survival after SRS depend significantly on the extent of the surgical resection of the primary tumor. The addition of temozolomide to radiotherapy prolongs survival in GBM patients. The relapse time affected significantly OS (p = 0.00008), but not survival after SRS. Neither OS, nor survival after SRS were affected significantly by such factors as the age of patients, the number of SRS fractions (one fraction vs several fractions), and target volume.

Conclusion: Radiosurgery improves the survival in patients with recurrent GBM. The extent of the surgical resection and adjuvant alkylating chemotherapy of the primary tumor, overall biologically effective dose and time between the primary diagnosis and SRS affect significantly the survival. The search for the more effective schedules for treating such patients requires further studies with more numerous cohorts of patients and extended follow-up.

复发性胶质母细胞瘤的放射外科治疗及影响治疗结果的预后因素。
背景:胶质母细胞瘤(GBM)是成人脑部最常见的恶性肿瘤,具有固有的侵袭性和高复发率。立体定向放射外科(SRS)目前被认为是GBM治疗的有效方式之一,可以在可接受的毒性水平下提高生存率。目的:探讨各种因素对GBM患者SRS术后生存的影响。患者和方法:我们回顾性分析了2014-2020年接受SRS治疗复发性GBM的68例患者的治疗结果。SRS配备Trilogy直线加速器(6mev)。对复发肿瘤/肿瘤持续生长的区域进行照射。对于原发性GBM的治疗,在联合替莫唑胺化疗的情况下,采用标准分步方案进行辅助放疗,总增强剂量为60 Gy,分为30次(Stupp方案)。36例患者接受替莫唑胺维持化疗。用于治疗复发性GBM的SRS以平均20.2 Gy的增强剂量提供,分为1-5次,平均单次剂量为12.4 Gy。生存率分析采用Kaplan-Meier法,log-rank检验用于评估独立预测因子对生存风险的影响。结果:中位总生存期(OS)为21.7个月(95%可信区间(CІ) 16.4-43.1), SRS后中位生存期为9.3个月(95% CІ 5.6-22.7)。大多数患者(72%)在SRS后存活至少6个月,约一半患者(48%)在原发肿瘤切除后存活至少24个月。SRS后的OS和生存率主要取决于原发肿瘤的手术切除程度。替莫唑胺加入放疗可延长GBM患者的生存期。复发时间对生存期有显著影响(p = 0.00008),但对生存期无显著影响。患者年龄、SRS分数(一个分数vs几个分数)、靶体积等因素对OS和SRS后生存率均无显著影响。结论:放疗可提高复发性GBM患者的生存率。原发肿瘤的手术切除和辅助烷基化化疗的范围、总生物有效剂量和原发诊断到SRS之间的时间对生存有显著影响。寻找治疗此类患者的更有效的方案需要进一步的研究,包括更多的患者队列和延长的随访时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Experimental oncology
Experimental oncology Medicine-Oncology
CiteScore
1.40
自引率
0.00%
发文量
49
期刊介绍: The Experimental Oncology is an English-language journal that publishes review articles, original contributions, short communications, case reports and technical advances presenting new data in the field of experimental and fundamental oncology. Manuscripts should be written in English, contain original work, which has not been published or submitted for publication elsewhere. It also implies the transfer of the Copyright from the author to “Experimental Oncology”. No part of journal publications may be reproduced, stored in a retrieval system or transmitted in any form or by any means without the prior permission of the publisher.
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