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临床试验/CTRI/2025/11/097775
CTRI/2025/11/097775尚未招募2 期

BIOlogically- guided Short-course HypOfractionated Radiation Therapy in poor-prognosis GBM (BIO-SHORT): A Prospective Phase 2 Randomised Control Trial

Tata Memorial Centre1 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2025年12月7日最近更新:

试验速览

阶段
2 期
状态
尚未招募
入组人数
108
试验地点
1

研究概览

简要总结

Study Type: Prospective Phase II Randomised Controlled Trial

Principal Investigator: Dr Abhishek Chatterjee

Study Site: Tata Memorial Centre, Mumbai

High grade gliomas, particularly glioblastoma, are among the most aggressive brain tumors and are associated with poor outcomes despite standard treatment. Many patients, especially older adults or those with poor general health, are not suitable for surgery and have a life expectancy of less than 12 months. Current standard includes a shortened course of radiotherapy (over 3 weeks) combined with chemotherapy using temozolomide (TMZ), which offers limited survival benefits. This study aims to explore whether delivering radiotherapy in a shorter duration (1 or 2 weeks) at a higher dose, guided by advanced imaging with a PET scan, can improve survival in this group of patients. PET scans help identify the most active parts of the tumor, which aids in targeting of these areas more precisely, potentially improving outcomes while reducing harm to healthy brain tissue. This study will randomly assign 116 eligible patients into two groups: • One group will receive the current standard of care (3-week radiotherapy + TMZ). • The other group will receive PET-guided radiotherapy over a shorter duration (either 5 or 10 sessions) at a higher dose, alongside TMZ. The primary goal is to compare overall survival at one year between the two groups. The study will also assess how the disease progresses, side effects of treatment, and the impact on patients’ quality of life. The study will be conducted over a total period of 6 years, including 4 years for patient enrolment and 2 years of follow-up. Participation in the study is entirely voluntary, and all patients will undergo an informed consent process. The study has been designed to follow all applicable ethical and regulatory guidelines. The results may help establish a more effective and convenient treatment option for patients with aggressive brain tumors and poor prognosis.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
50.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Patients with biopsy proven IDH wild type GBM or imaging defined GBM Neurological Predictor Scale (NPS) 2-3 Unfit for surgery and referred for direct RT Age greater tuan equal to 50 years.

排除标准

  • IDH mutant glioma Histone altered glioma Multifocal disease or Gliomatosis like appearance which necessitates whole brain RT Disseminated disease in brain or spine NPS = 0-1 or = 4 Karnofsky Performance Status score less than 50(Patient requires considerable assistance and frequent medical care) Prior administration of any systemic therapy directed against glioma (eg.Temozolomide, CCNU, Bevacizumab).

研究者

申办方类型
Other [Research institution and hospital ]
责任方
Principal Investigator
主要研究者

Dr Abhishek Chatterjee

Tata Memorial Centre

研究点 (1)

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