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Radiation Therapy With or Without Temozolomide in Treating Older Patients With Newly Diagnosed Glioblastoma Multiforme

A Randomized Phase III Study of Temozolomide and Short-Course Radiation Versus Short-Course Radiation Alone In The Treatment of Newly Diagnosed Glioblastoma Multiforme in Elderly Patients

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00482677
Enrollment
562
Registered
2007-06-05
Start date
2007-11-14
Completion date
2016-08-10
Last updated
2023-08-22

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

Conditions

Brain and Central Nervous System Tumors

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

DRUGtemozolomide

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.

GENETICDNA 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

PROCEDUREquality-of-life assessment

prior to randomization until end of study

RADIATIONRadiation

Short course radiotherapy

Sponsors

European Organisation for Research and Treatment of Cancer - EORTC
CollaboratorNETWORK
Trans Tasman Radiation Oncology Group
CollaboratorOTHER
Canadian Cancer Trials Group
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to 120 Years
Healthy volunteers
No

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

MeasureTime frameDescription
Overall Survival7 yearsTime from date of randomization to the date of death of any causes, or censored at last known alive date.

Secondary

MeasureTime frameDescription
Progression-free Survival7 yearsTime from date of randomization to the date of disease progression or death whichever came first, or censored at last disease assessment date.
Adverse Events7 yearsEvaluated according to CTCAE V3.0
Methylation Status of the O6-methylguanine-DNA Methyltransferase Promoter7 yearsOverall survival for patients by Methylation status of the O6-methylguanine-DNA methyltransferase promoter

Countries

Canada, Germany, Japan, Netherlands

Participant flow

Participants by arm

ArmCount
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
Total562

Baseline characteristics

CharacteristicTemozolomideRadiationTotal
Age, Continuous73 years73 years73 years
ECOG Performance Status
0, 1
215 Participants217 Participants432 Participants
ECOG Performance Status
2
66 Participants64 Participants130 Participants
Mini Mental Status Examination27 participants27 participants27 participants
Region of Enrollment
Canada
101 participants98 participants199 participants
Region of Enrollment
Germany
124 participants125 participants249 participants
Region of Enrollment
Japan
8 participants9 participants17 participants
Region of Enrollment
Netherlands
48 participants49 participants97 participants
Resection
Biopsy only
84 Participants82 Participants166 Participants
Resection
Complete/incomplete resection
197 Participants199 Participants396 Participants
Sex: Female, Male
Female
110 Participants109 Participants219 Participants
Sex: Female, Male
Male
171 Participants172 Participants343 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
260 / 271256 / 271
serious
Total, serious adverse events
158 / 271135 / 271

Outcome results

Primary

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

ArmMeasureValue (MEDIAN)
TemozolomideOverall Survival9.33 Months
RadiationOverall Survival7.62 Months
Secondary

Adverse Events

Evaluated according to CTCAE V3.0

Time frame: 7 years

Secondary

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.

ArmMeasureValue (MEDIAN)
TemozolomideMethylation Status of the O6-methylguanine-DNA Methyltransferase Promoter13.47 Months
RadiationMethylation Status of the O6-methylguanine-DNA Methyltransferase Promoter7.69 Months
Secondary

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

ArmMeasureValue (MEDIAN)
TemozolomideProgression-free Survival5.29 Months
RadiationProgression-free Survival3.94 Months

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026