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Title: 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)
Authors: Arakawa, Yoshiki  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0003-4626-4645 (unconfirmed)
Sasaki, Keita
Mineharu, Yohei  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-6346-3999 (unconfirmed)
Uto, Megumi  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0003-1542-2671 (unconfirmed)
Mizowaki, Takashi  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-8135-8746 (unconfirmed)
Mizusawa, Junki
Sekino, Yuta
Ono, Tomohiro
Aoyama, Hidefumi
Satomi, Kaishi
Ichimura, Koichi
Kinoshita, Manabu
Ohno, Makoto
Ito, Yoshinori
Nishikawa, Ryo
Fukuda, Haruhiko
Nishimura, Yasumasa
Narita, Yoshitaka
Brain Tumor Study Group and Radiation Therapy Study Group of the Japan Clinical Oncology Group
Author's alias: 荒川, 芳輝
峰晴, 陽平
宇藤, 恵
溝脇, 尚志
小野, 智博
Keywords: Randomized controlled trial
Glioblastoma
Elderly
Temozolomide
Short-course radiotherapy
Issue Date: 2021
Publisher: Springer Nature
BMC
Journal title: BMC Cancer
Volume: 21
Thesis number: 1105
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/m2/day, 5 days) and adjuvant temozolomide over 40 Gy in 15 fractions with concomitant (75 mg/m2/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.
Rights: © The Author(s). 2021
This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
URI: http://hdl.handle.net/2433/277889
DOI(Published Version): 10.1186/s12885-021-08834-0
PubMed ID: 34654402
Appears in Collections:Journal Articles

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