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一项随机 III 期研究,评估短程放疗联合替莫唑胺治疗新诊断的老年胶质母细胞瘤患者的疗效:日本癌症研究集团研究 JCOG1910(老年Gli o-PIII)。

A randomized phase III study of short-course radiotherapy combined with Temozolomide in elderly patients with newly diagnosed glioblastoma; Japan clinical oncology group study JCOG1910 (AgedGlio-PIII).

机构信息

Department of Neurosurgery, Kyoto University Graduate School of Medicine, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.

JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.

出版信息

BMC Cancer. 2021 Oct 15;21(1):1105. doi: 10.1186/s12885-021-08834-0.

Abstract

BACKGROUND

The current standard treatment for elderly patients with newly diagnosed glioblastoma is surgery followed by short-course radiotherapy with temozolomide. In recent studies, 40 Gy in 15 fractions vs. 60 Gy in 30 fractions, 34 Gy in 10 fractions vs. 60 Gy in 30 fractions, and 40 Gy in 15 fractions vs. 25 Gy in 5 fractions have been reported as non-inferior. The addition of temozolomide increased the survival benefit of radiotherapy with 40 Gy in 15 fractions. However, the optimal regimen for radiotherapy plus concomitant temozolomide remains unresolved.

METHODS

This multi-institutional randomized phase III trial was commenced to confirm the non-inferiority of radiotherapy comprising 25 Gy in 5 fractions with concomitant (150 mg/m/day, 5 days) and adjuvant temozolomide over 40 Gy in 15 fractions with concomitant (75 mg/m/day, every day from first to last day of radiation) and adjuvant temozolomide in terms of overall survival (OS) in elderly patients with newly diagnosed glioblastoma. A total of 270 patients will be accrued from 51 Japanese institutions in 4 years and follow-up will last 2 years. Patients 71 years of age or older, or 71-75 years old with resection of less than 90% of the contrast-enhanced region, will be registered and randomly assigned to each group with 1:1 allocation. The primary endpoint is OS, and the secondary endpoints are progression-free survival, frequency of adverse events, proportion of Karnofsky performance status preservation, and proportion of health-related quality of life preservation. The Japan Clinical Oncology Group Protocol Review Committee approved this study protocol in April 2020. Ethics approval was granted by the National Cancer Center Hospital Certified Review Board. Patient enrollment began in August 2020.

DISCUSSION

If the primary endpoint is met, short-course radiotherapy comprising 25 Gy in 5 fractions with concomitant and adjuvant temozolomide will be a standard of care for elderly patients with newly diagnosed glioblastoma.

TRIAL REGISTRATION

Registry number: jRCTs031200099 . Date of Registration: 27/Aug/2020. Date of First Participant Enrollment: 4/Sep/2020.

摘要

背景

对于新诊断的老年胶质母细胞瘤患者,目前的标准治疗方法是手术联合替莫唑胺短程放疗。最近的研究表明,40Gy/15 次分割与 60Gy/30 次分割、34Gy/10 次分割与 60Gy/30 次分割、40Gy/15 次分割与 25Gy/5 次分割的疗效相当。替莫唑胺的加入增加了 40Gy/15 次分割放疗的生存获益。然而,放疗联合替莫唑胺的最佳方案仍未解决。

方法

本多中心随机 III 期临床试验旨在证实 25Gy/5 次分割放疗联合同期(150mg/m/天,连用 5 天)和辅助替莫唑胺与 40Gy/15 次分割放疗联合同期(75mg/m/天,从放疗第一天到最后一天连用)和辅助替莫唑胺在新诊断的老年胶质母细胞瘤患者中的总生存期(OS)方面的非劣效性。该研究将在 4 年内从 51 家日本机构招募 270 名患者,并进行 2 年的随访。71 岁及以上或 71-75 岁且切除的增强区域小于 90%的患者将被登记并随机分配到每组,1:1 分配。主要终点是 OS,次要终点是无进展生存期、不良事件发生率、卡氏功能状态保留率和健康相关生活质量保留率。日本临床肿瘤学组方案审查委员会于 2020 年 4 月批准了该研究方案。国家癌症中心医院认证审查委员会批准了该研究方案。患者招募于 2020 年 8 月开始。

讨论

如果主要终点达到,25Gy/5 次分割放疗联合同期和辅助替莫唑胺将成为新诊断的老年胶质母细胞瘤患者的标准治疗方法。

试验注册

注册号:jRCTs031200099。注册日期:2020 年 8 月 27 日。首例患者入组日期:2020 年 9 月 4 日。

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