Temozolomide Plus Bevacizumab in Supratentorial Glioblastoma in 70 Years and Older Patients With an Impaired Functional Status
ATAG
1 other identifier
interventional
70
1 country
1
Brief Summary
The optimal treatment of glioblastoma multiforme (GBM) in patients aged ≥70 years with a Karnofsky performance status (KPS) \<70 is unestablished. This clinical trial evaluated the efficacy and safety of upfront temozolomide (TMZ) and bevacizumab (Bev) in patients aged ≥70 years and a KPS \<70.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_2
Started Oct 2010
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2013
CompletedFirst Submitted
Initial submission to the registry
July 31, 2016
CompletedFirst Posted
Study publicly available on registry
September 13, 2016
CompletedSeptember 13, 2016
July 1, 2016
2.6 years
July 31, 2016
September 7, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Median Overall Survival (OS)
OS calculated from the date of surgery until death from any cause or up to 36 months.
OS calculated from the date of surgery until death or up to 36 months.
Secondary Outcomes (6)
Progression-free survival (PFS)
PFS calculated from the date of surgery until the date of first documented progression or up to 36 months.
Toxicity grade according to the National Cancer Institute Common Toxicity Criteria (NCI CTCAE, version 3.0)
Assessment every 2 weeks until 12 months
Health-related quality of life using QLQ-C30 questionnaire
at baseline and every month until 12 months
Health-related quality of life using QLQ-BN20
at baseline and every month until 12 months
Cognitive assessment MMSEs
at baseline and they were repeated every month until 12 months
- +1 more secondary outcomes
Study Arms (1)
Temozolomide and Bevacizumab
EXPERIMENTALSingle experimental arm with two drugs : Temozolomide and Bevacizumab
Interventions
Temozolomide (TMZ) Temozolomide (TMZ) administered at 130-150 mg/m2 for 5 consecutive days every 4 weeks up to 12 cycles. IV or oral administration was allowed according to the clinical status. TMZ starts at 130 mgs/m2 and increase to 150 mgs/m2 during the second cycle in the absence of hematologic toxicity. In the case of grade 3 or 4 toxicity, the dose for the next cycle is decreased to 110 mg/m2. If the grade 3 or 4 toxicity persists at a dose of 110 mg/m2, treatment is discontinued.
Bevacizumab (Bev) administered at a dose of 10 mgs/kg every 2 weeks. Bev was interrupted in cases of wound healing disturbances, gastrointestinal perforation, intestinal occlusion, fistula, uncontrolled hypertension, nephrotic syndrome, grade 4 or recurrent grade 3 thromboembolic events, arterial thrombosis, hemorrhage \> grade 2, left ventricular failure, or posterior reversible leukoencephalopathy.
Eligibility Criteria
You may qualify if:
- Supratentorial Glioblastoma diagnosed by biopsy.
- Patients aged ≥ 70 years
- KPS \>30 and \< 70
- Life expectancy \> or = 8 weeks
- Patients were enrolled at least 14 days after stereotactic biopsy and 28 days after surgical biopsy.
- CT or brain MRI was performed within 4 weeks before treatment to rule out haemorrhage.
- Included to health social security system
- Informed consent form
You may not qualify if:
- Previous treatment with Surgical resection, RT or chemotherapy to the tumor.
- Hemoglobin level \< 9 g%
- Absolute neutrophil count \< 1500
- Platelet count \< 100.000
- ASAT or ALAT levels more than 3 times the upper limit of normal.
- Bilirubin levels more than 2 times the upper limit of normal
- Creatinin more than 1.5 times the upper limit of normal
- Untreated high blood pressure \>150/100 mmHg
- Congestive cardiac failure
- Proteinuria \> 1 gr/24h
- INR \> 1.5 the upper limit of normal
- Recent symptomatic haemorrhage
- History of abnormal wound healing
- Gastrointestinal fistula
- Haemoptysis \> grade 2 (NCI-CTC)
- +6 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Assistance Publique - Hôpitaux de Parislead
- Roche Pharma AGcollaborator
Study Sites (1)
Groupe Hospitalier Pitié-Salpêtrière
Paris, Paris, 75013, France
Related Publications (20)
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PMID: 25035291BACKGROUNDStupp R, Mason WP, van den Bent MJ, Weller M, Fisher B, Taphoorn MJ, Belanger K, Brandes AA, Marosi C, Bogdahn U, Curschmann J, Janzer RC, Ludwin SK, Gorlia T, Allgeier A, Lacombe D, Cairncross JG, Eisenhauer E, Mirimanoff RO; European Organisation for Research and Treatment of Cancer Brain Tumor and Radiotherapy Groups; National Cancer Institute of Canada Clinical Trials Group. Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med. 2005 Mar 10;352(10):987-96. doi: 10.1056/NEJMoa043330.
PMID: 15758009BACKGROUNDLou E, Peters KB, Sumrall AL, Desjardins A, Reardon DA, Lipp ES, Herndon JE 2nd, Coan A, Bailey L, Turner S, Friedman HS, Vredenburgh JJ. Phase II trial of upfront bevacizumab and temozolomide for unresectable or multifocal glioblastoma. Cancer Med. 2013 Apr;2(2):185-95. doi: 10.1002/cam4.58. Epub 2013 Jan 24.
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PMID: 29472310DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jean-Yves Delattre, MD-PhD
Pôle MSN, Groupe Hospitalier Pitié-Salpêtrière
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 31, 2016
First Posted
September 13, 2016
Study Start
October 1, 2010
Primary Completion
May 1, 2013
Study Completion
June 1, 2013
Last Updated
September 13, 2016
Record last verified: 2016-07
Data Sharing
- IPD Sharing
- Will not share