Brain and Central Nervous System Tumors
Conditions
Keywords
adult glioblastoma, adult giant cell glioblastoma, adult gliosarcoma
Brief summary
RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving radiation therapy together with temozolomide may kill more tumor cells. It is not yet known whether radiation therapy and temozolomide are more effective than radiation therapy alone in treating glioblastoma multiforme. PURPOSE: This randomized phase III trial is studying radiation therapy and temozolomide to see how well they work compared with radiation therapy alone in treating patients with newly diagnosed glioblastoma multiforme.
Detailed description
OBJECTIVES: Primary * Compare overall survival rates in older patients with newly diagnosed glioblastoma multiforme treated with short-course radiotherapy with or without temozolomide. Secondary * Compare progression-free survival of patients treated with these regimens. * Compare the nature, severity, and frequency of adverse events in patients treated with these regimens. * Compare the quality of life of patient treated with these regimens. * Determine the methylation status of the O6-methylguanine-DNA methyltransferase promoter. OUTLINE: This is a multicenter, randomized study. Patients are stratified according to center, age (65-70 years vs 71-75 years vs ≥ 76 years), ECOG performance status (0-1 vs 2), and extent of resection at surgery (biopsy only vs complete or incomplete resection). Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients undergo radiotherapy once daily on days 1-5, 8-12, and 15-19 in the absence of disease progression or unacceptable toxicity. * Arm II: Patients undergo radiotherapy as in arm I and receive oral temozolomide once daily on days 1-25. Beginning 4 weeks after completion of radiotherapy and temozolomide, patients receive adjuvant oral temozolomide once daily on days 1-5. Treatment with temozolomide alone repeats every 28 days for up to 12 months in the absence of disease progression or unacceptable toxicity. Patients complete quality of life questionnaires at baseline and periodically during study treatment. Tissue samples are collected at baseline and analyzed for methylation status of the O6-methylguanine-DNA methyltransferase promoter. After completion of study treatment, patients are followed every 3 months.
Interventions
Temozolomide (concurrent with radiation) 75 mg/m2 PO 3 weeks once a day, daily, from the first day to the last day of radiotherapy, but for no longer than 28 days, and then adjuvantly for up to 12 cycles (150 mg/m2 for the first 5 days of each cycle). Adjuvant TMZ may be escalated to 200mg/m2 in C2 onward if appropriate.
A stratified log-rank test, adjusting for the stratification factors (except centre) plus MGMT promoter methylation status, will be used as the primary method to compare the overall survival between the two arms
prior to randomization until end of study
Short course radiotherapy
Sponsors
Study design
Eligibility
Inclusion criteria
DISEASE CHARACTERISTICS: * Histopathologically confirmed glioblastoma multiforme * Grade IV disease by WHO classification * Newly diagnosed disease * Initial diagnostic surgery or biopsy performed within the past 4 weeks * Not a candidate for standard radiotherapy (60Gy/30 fractions over 6 weeks) in combination with temozolomide PATIENT CHARACTERISTICS: * ECOG performance status 0-2 * Absolute granulocyte count ≥ 1,500/mm³ * Platelet count ≥ 100,000/mm³ * Creatinine ≤ 1.5 times upper limit of normal (ULN) * Bilirubin ≤ 1.5 times ULN * ALT and AST \< 2.5 times ULN * No known hypersensitivity to temozolomide or compounds with similar chemical composition to temozolomide * No history of other malignancies except adequately treated nonmelanoma skin cancer, curatively treated in situ cancer of the cervix, or other curatively treated solid tumors with no evidence of disease for at least 5 years * No serious active infection (e.g., wound infection requiring parenteral antibiotics) or other serious underlying medical conditions that would preclude study treatment * No other condition (e.g., psychological or geographical) that would preclude study compliance PRIOR CONCURRENT THERAPY: * No prior chemotherapy * No prior radiotherapy * No prior or concurrent investigational therapy * No concurrent surgical procedures for tumor debulking * No concurrent stereotactic boost radiotherapy * No other concurrent chemotherapy, immunotherapy, or biological therapy * No concurrent epoetin alfa * Concurrent corticosteroids allowed provided the patient has been on a stable or decreasing dose for at least 14 days
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Overall Survival | 7 years | Time from date of randomization to the date of death of any causes, or censored at last known alive date. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free Survival | 7 years | Time from date of randomization to the date of disease progression or death whichever came first, or censored at last disease assessment date. |
| Adverse Events | 7 years | Evaluated according to CTCAE V3.0 |
| Methylation Status of the O6-methylguanine-DNA Methyltransferase Promoter | 7 years | Overall survival for patients by Methylation status of the O6-methylguanine-DNA methyltransferase promoter |
Countries
Canada, Germany, Japan, Netherlands
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Temozolomide Temozolomide and short course radiation
temozolomide: Temozolomide (concurrent with radiation) 75 mg/m2 PO 3 weeks once a day, daily, from the first day to the last day of radiotherapy, but for no longer than 28 days, and then adjuvantly for up to 12 cycles (150 mg/m2 for the first 5 days of each cycle). Adjuvant TMZ may be escalated to 200mg/m2 in C2 onward if appropriate.
DNA methylation analysis: A stratified log-rank test, adjusting for the stratification factors (except centre) plus MGMT promoter methylation status, will be used as the primary method to compare the overall survival between the two arms
quality-of-life assessment: prior to randomization until end of study | 281 |
| Radiation Short course radiation alone
DNA methylation analysis: A stratified log-rank test, adjusting for the stratification factors (except centre) plus MGMT promoter methylation status, will be used as the primary method to compare the overall survival between the two arms
quality-of-life assessment: prior to randomization until end of study
Radiation: Short course radiotherapy | 281 |
| Total | 562 |
Baseline characteristics
| Characteristic | Temozolomide | Radiation | Total |
|---|---|---|---|
| Age, Continuous | 73 years | 73 years | 73 years |
| ECOG Performance Status 0, 1 | 215 Participants | 217 Participants | 432 Participants |
| ECOG Performance Status 2 | 66 Participants | 64 Participants | 130 Participants |
| Mini Mental Status Examination | 27 participants | 27 participants | 27 participants |
| Region of Enrollment Canada | 101 participants | 98 participants | 199 participants |
| Region of Enrollment Germany | 124 participants | 125 participants | 249 participants |
| Region of Enrollment Japan | 8 participants | 9 participants | 17 participants |
| Region of Enrollment Netherlands | 48 participants | 49 participants | 97 participants |
| Resection Biopsy only | 84 Participants | 82 Participants | 166 Participants |
| Resection Complete/incomplete resection | 197 Participants | 199 Participants | 396 Participants |
| Sex: Female, Male Female | 110 Participants | 109 Participants | 219 Participants |
| Sex: Female, Male Male | 171 Participants | 172 Participants | 343 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 260 / 271 | 256 / 271 |
| serious Total, serious adverse events | 158 / 271 | 135 / 271 |
Outcome results
Overall Survival
Time from date of randomization to the date of death of any causes, or censored at last known alive date.
Time frame: 7 years
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Temozolomide | Overall Survival | 9.33 Months |
| Radiation | Overall Survival | 7.62 Months |
Adverse Events
Evaluated according to CTCAE V3.0
Time frame: 7 years
Methylation Status of the O6-methylguanine-DNA Methyltransferase Promoter
Overall survival for patients by Methylation status of the O6-methylguanine-DNA methyltransferase promoter
Time frame: 7 years
Population: Patients with MGMT promoter methylated.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Temozolomide | Methylation Status of the O6-methylguanine-DNA Methyltransferase Promoter | 13.47 Months |
| Radiation | Methylation Status of the O6-methylguanine-DNA Methyltransferase Promoter | 7.69 Months |
Progression-free Survival
Time from date of randomization to the date of disease progression or death whichever came first, or censored at last disease assessment date.
Time frame: 7 years
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Temozolomide | Progression-free Survival | 5.29 Months |
| Radiation | Progression-free Survival | 3.94 Months |