Prolonged Adjuvant Temozolomide vs "Stop & Go" in Glioblastoma Patients (PATSGO)
Primary Purpose
Glioblastoma
Status
Unknown status
Phase
Phase 2
Locations
Belgium
Study Type
Interventional
Intervention
Temozolomide
Temozolomide
Sponsored by
About this trial
This is an interventional treatment trial for Glioblastoma focused on measuring Temozolomide, Phase II, Chemotherapy, Glioblastoma, Progression-free Survival
Eligibility Criteria
Inclusion Criteria:
- Patients with histologically confirmed diagnosis of GBM
- Availability of pre-treatment GBM tissue to determine the activation status of MGMT gene is not mandatory but strongly recommended
- Patients must have received radiation and TMZ for 6 weeks followed by 6 months of TMZ. Randomization should be performed within the 6 weeks after the last chemotherapy.
- A brain MRI with or without a PET-Scan-methionine must be performed before enrolment.
- Age ≥ 18 years
- Karnofsky Performance status ≥ 60
- Normal haematological functions: ANC ≥ 1.5 x 109cells/l, platelets ≥ 100 x 109 cells/l
- Normal liver function: total bilirubin < 1.5 x ULN, alkaline phosphatase and transaminases (ASAT/ALAT) < 2.5 times the upper limit of the normal range
- Serum creatinine < 1.5 x ULN
- Clinically normal cardiac function without history of ischemic heart disease in the past 12 months. Absence of cardiac insufficiency NYHA grade III and IV, instable angina, arrhythmia
- No previous or current malignancy (except treated basal or squamous cell skin carcinoma, cervix cancer or in situ carcinoma of the breast).
- All patients (male and female) with reproductive potential must use effective contraception. Females must have a negative serum pregnancy test at entry to study.
- Signed informed consent from the patient or legal representative must be obtained.
Exclusion Criteria:
All non inclusion criteria
Sites / Locations
- Cliniques Universitaires Saint-LucRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Other
Arm Label
A: prolonged adj TMZ
B : Stop and Go
Arm Description
Rechallenging patients with TMZ at relapse
Outcomes
Primary Outcome Measures
to determine whether prolonged administration of Temozolomide in glioblastoma patients increase their progression-free and overall survival at 6 months
Secondary Outcome Measures
safety and adverse event profile of prolonged adjuvant Temozolomide
Full Information
NCT ID
NCT00643825
First Posted
March 20, 2008
Last Updated
July 22, 2010
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
1. Study Identification
Unique Protocol Identification Number
NCT00643825
Brief Title
Prolonged Adjuvant Temozolomide vs "Stop & Go" in Glioblastoma Patients
Acronym
PATSGO
Official Title
Randomized Multicentric Phase II Study of Prolonged Adjuvant Temozolomide or "Stop and Go" in Glioblastoma Patients: The PATSGO Study
Study Type
Interventional
2. Study Status
Record Verification Date
July 2010
Overall Recruitment Status
Unknown status
Study Start Date
January 2008 (undefined)
Primary Completion Date
January 2011 (Anticipated)
Study Completion Date
January 2012 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study will test the hypothesis that prolonged adjuvant Temozolomide (TMZ) may delay relapses in patients with glioblastoma compared to the standard care consisting in observation with brain MRI every 3 months and rechallenging with TMZ at relapse (Stop and Go arm).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma
Keywords
Temozolomide, Phase II, Chemotherapy, Glioblastoma, Progression-free Survival
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
A: prolonged adj TMZ
Arm Type
Active Comparator
Arm Title
B : Stop and Go
Arm Type
Other
Arm Description
Rechallenging patients with TMZ at relapse
Intervention Type
Drug
Intervention Name(s)
Temozolomide
Other Intervention Name(s)
TEMODAR, TEMODAL
Intervention Description
Capsules 5,10,20,100,250 mg 200mg/m2/day , 5days per 28 till PD
Intervention Type
Drug
Intervention Name(s)
Temozolomide
Other Intervention Name(s)
TEMODAR, TEMODAL
Intervention Description
Observation till Progression then rechallenging with TMZ
Primary Outcome Measure Information:
Title
to determine whether prolonged administration of Temozolomide in glioblastoma patients increase their progression-free and overall survival at 6 months
Time Frame
36 months
Secondary Outcome Measure Information:
Title
safety and adverse event profile of prolonged adjuvant Temozolomide
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with histologically confirmed diagnosis of GBM
Availability of pre-treatment GBM tissue to determine the activation status of MGMT gene is not mandatory but strongly recommended
Patients must have received radiation and TMZ for 6 weeks followed by 6 months of TMZ. Randomization should be performed within the 6 weeks after the last chemotherapy.
A brain MRI with or without a PET-Scan-methionine must be performed before enrolment.
Age ≥ 18 years
Karnofsky Performance status ≥ 60
Normal haematological functions: ANC ≥ 1.5 x 109cells/l, platelets ≥ 100 x 109 cells/l
Normal liver function: total bilirubin < 1.5 x ULN, alkaline phosphatase and transaminases (ASAT/ALAT) < 2.5 times the upper limit of the normal range
Serum creatinine < 1.5 x ULN
Clinically normal cardiac function without history of ischemic heart disease in the past 12 months. Absence of cardiac insufficiency NYHA grade III and IV, instable angina, arrhythmia
No previous or current malignancy (except treated basal or squamous cell skin carcinoma, cervix cancer or in situ carcinoma of the breast).
All patients (male and female) with reproductive potential must use effective contraception. Females must have a negative serum pregnancy test at entry to study.
Signed informed consent from the patient or legal representative must be obtained.
Exclusion Criteria:
All non inclusion criteria
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean-Francois BAURAIN, MD, PhD
Phone
+32 2 764 54 71
Email
jean-francois.baurain@uclouvain.be
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Francois Baurain, MD, PhD
Organizational Affiliation
Cliniques universitaires Saint-Luc
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cliniques Universitaires Saint-Luc
City
Brussels
State/Province
Europe
ZIP/Postal Code
1200
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Francois BAURAIN, MD, PhD
Phone
+32 2 764 54 71
Email
jean-francois.baurain@@uclouvain.be
12. IPD Sharing Statement
Learn more about this trial
Prolonged Adjuvant Temozolomide vs "Stop & Go" in Glioblastoma Patients
We'll reach out to this number within 24 hrs