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Daily Temozolomide for Elderly Patients With Unmethylated MGMT- Promoter Newly Diagnosed GliOblatoma

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Glioblastoma is an aggressive type of brain cancer. Standard treatment usually includes three weeks of radiation therapy alone or combined with chemotherapy using Temozolomide. After a four- to six-week break, more Temozolomide chemotherapy is usually given. However, some tumors have a marker (unmethylated MGMT) that predicts the usual chemotherapy won't work. Because of this, this project will explore other treatment options to help slow the disease and improve survival. In this study, the same chemotherapy (Temozolomide) normally given after radiation therapy for glioblastoma. The only difference is that it will be given with a modified regimen.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 65
Healthy Volunteers: f
View:

• Age ≥65 years.

• Histopathologically confirmed newly diagnosed WHO grade 4, IDH wild-type GBM

• Unmethylated MGMT promoter, according to local assessment

• Completed treatment with 40 Gy in 15 fractions over three weeks, with concurrent TMZ, within six weeks prior to enrollment

• Eastern Cooperative Oncology Group (ECOG) performance status scale of 0, 1, or 2.

• Karnofsky Performance Status (KPS) ≥60.

• Adequate organ function, as defined by the following laboratory values obtained within 28 days prior to enrollment:

‣ Absolute neutrophil count (ANC) \>1.5 × 10⁹/L (1,500 cells/mm³).

⁃ Platelet count \>100 × 10⁹/L (100,000 cells/mm³).

⁃ Serum creatinine \<1.5 times the upper limit of normal.

⁃ Total serum bilirubin \<1.5 times the upper limit of normal.

⁃ ALT (SGPT) \<2.5 times the upper limit of normal and/or AST (SGOT) \<2.5 times the upper limit of normal.

• Signed informed consent (and assent, if applicable) must be obtained from the participant or their legal representative, ensuring the participant's ability to adhere to the study requirements.

Locations
Other Locations
Canada
Sunnybrook Health Sciences Centre
RECRUITING
Toronto
Time Frame
Start Date: 2025-11-01
Estimated Completion Date: 2029-11
Participants
Target number of participants: 118
Treatments
Experimental: Treatment
Daily TMZ
Sponsors
Leads: Sunnybrook Health Sciences Centre

This content was sourced from clinicaltrials.gov