Skip to content

A study of factors affecting survival in adults with high grade brain tumors

Impact of Tumor and Treatment Factors, Including Overall Treatment Time and Surgery-to-Radiotherapy Interval, on Survival Outcomes in Adult High-Grade Glioma - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/07/113565
Enrollment
200
Registered
2026-07-07
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C719- Malignant neoplasm of brain, unspecified

Interventions

Intervention1: Nil: Nil

Sponsors

Dr Ashutosh Mukherji
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 18 years or older. Histologically confirmed diffuse adult type high grade gliomas WHO Grade 3 or WHO Grade 4 and IDH wild type adult diffuse Grade 2 gliomas as per WHO 2021 classification. IDH wild type adult diffuse gliomas meeting molecular criteria for glioblastoma WHO Grade 4. Patients who have undergone surgical resection or biopsy followed by curative intent radiotherapy with or without chemotherapy. Patients treated at MPMMCC and HBCH Varanasi or referred for curative intent radiotherapy. Availability of complete clinical radiological pathological and treatment records. Availability of radiotherapy planning and dosimetric data in ARIA Eclipse for relevant analyses. Patients willing to provide written informed consent.

Exclusion criteria

Exclusion criteria: Low grade gliomas WHO Grade 1 or WHO Grade 2 and pediatric type gliomas. Gliomas of the brainstem optic pathway or spinal cord. Non diffuse or circumscribed gliomas as per WHO 2021 classification. Recurrent gliomas previously treated with cranial radiotherapy. Patients who received definitive treatment entirely outside the study institution without adequate records. Patients with concurrent malignancies affecting survival outcomes. Patients unwilling or unable to provide informed consent for the study.

Design outcomes

Primary

MeasureTime frame
Progression Free Survival defined as the time from surgery to first documented disease progression recurrence or death from any cause whichever occurs first.Timepoint: Up to 18 months from date of inclusion or until disease progression recurrence death or end of study whichever occurs earlier.

Secondary

MeasureTime frame
Overall survival at 18 months.Timepoint: 18 months after inclusion or until death whichever occurs earlier.;Patterns of disease recurrence including local marginal and distant recurrence.Timepoint: Assessed throughout follow up up to 18 months.;Treatment related toxicities including radionecrosis gliosis and chemotherapy related toxicities.Timepoint: Assessed throughout follow up up to 18 months.

Countries

India

Contacts

Public ContactAshutosh Mukherji

Mahamana Madan Mohan Malaviya Cancer Centre and Homi Bhabha Cancer Hospital Varanasi

alan_john010@outlook.com8129975484

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026