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Phase-1 Study of Folinic Acid to Modulate MGMT Gene in Glioblastoma (FOLAGLI)

Primary Purpose

Grade IV Astrocytoma, Glioblastoma

Status
Terminated
Phase
Phase 1
Locations
France
Study Type
Interventional
Intervention
Temozolomide
folinic acid at pharmacological dose is the escalated drug
High voltage radiation therapy (linear accelerator)
Sponsored by
Institut Cancerologie de l'Ouest
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Grade IV Astrocytoma focused on measuring high-grade, glioma, epigenetic

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Operated GBM (complete or near complete resection)
  • Un-methylated MGMT gene

Exclusion Criteria:

  • Non operable GBM
  • Methylated MGMT

Sites / Locations

  • Institut de Cacerologie de l'ouest - site Paul Papin
  • CHU de Lyon
  • ICO site Gauducheau
  • CLCC Antoine Lacassagne

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Folinic Acid

Arm Description

Folinic acid is given orally every day during the radiation therapy (47 days), then 5 days at each of the 6 maintenance cycle of temozolomide. The dose is escalated in a "3x3" method and the levels are: 5mg, 10mg, 15mg, 30mg, 60mg.

Outcomes

Primary Outcome Measures

Maximal Tolerated Dose
maximal tolerated dose 3x3 patients inclusion(modified Fibonnacci dose escalation )

Secondary Outcome Measures

MGMT gene re-methylation
MGMT gene re-methylation in tumoral and blood samples

Full Information

First Posted
September 12, 2012
Last Updated
February 20, 2023
Sponsor
Institut Cancerologie de l'Ouest
Collaborators
Centre Antoine Lacassagne, Hospices Civils de Lyon
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1. Study Identification

Unique Protocol Identification Number
NCT01700569
Brief Title
Phase-1 Study of Folinic Acid to Modulate MGMT Gene in Glioblastoma
Acronym
FOLAGLI
Official Title
Phase I Study of Escalated Pharmacologic Dose, of Oral Folinic Acid in Combination With Temozolomide, According to Stupp R. Regimen, in Patients With Operated Grade-IV Astocytoma and a Non-methylated Gene Status of MGMT.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Terminated
Why Stopped
changing the standard of care
Study Start Date
January 2013 (Actual)
Primary Completion Date
December 12, 2019 (Actual)
Study Completion Date
April 16, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Cancerologie de l'Ouest
Collaborators
Centre Antoine Lacassagne, Hospices Civils de Lyon

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
O6-méthylguanine méthyltransférase (MGMT) is the main repair gene after DNA lesion induced by Temozolomide in combination with radiation therapy of Glioblastoma (GBM) in Stupp.R et al published regimen. In preclinical models, it has been demonstrated that MGMT methylation (which is silencing the DNA repair process) is achievable by folic acid. About half of the patients with operated GBM have an un-methylated MGMT gene status and therefore a poorer prognosis. A phase-1 dose escalation study is proposed with pharmacologic doses of folinic acid in combination with temozolomide and radiotherapy of operated GBM.
Detailed Description
Glioblastoma treated by Stupp regimen (Temozolomide + radiation therapy) have a different outcome depending on the methylation status of MGMT gene: when the gene is unmethylated, the repair process is active and the prognostic poor. In pre-clinical models, it has been demonstrated that Folic acid could re-methylate the MGMT gene and therefore the repair process to radiation and temozolomide could be limited, allowing a better prognosis. The proposed phase-1 study will explore the safety and efficacy of escalated doses of oral Folinic acid concomitantly with Stupp regimen. To determine the MTD is the main objective of the study, then the toxicty profile, the RDP2 and the methylation process efficacy at the MGMT gene level.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Grade IV Astrocytoma, Glioblastoma
Keywords
high-grade, glioma, epigenetic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Folinic Acid
Arm Type
Experimental
Arm Description
Folinic acid is given orally every day during the radiation therapy (47 days), then 5 days at each of the 6 maintenance cycle of temozolomide. The dose is escalated in a "3x3" method and the levels are: 5mg, 10mg, 15mg, 30mg, 60mg.
Intervention Type
Drug
Intervention Name(s)
Temozolomide
Other Intervention Name(s)
Temodal, capsule dosage available: 5, 20, 10, 180 and 250 mg
Intervention Description
All the Patients are treated by oral Temozolomide 75 mg/m²/day every day during 42 days, 30 minutes after Folinic acid and 120 min before the radiation dose to the brain tumor. After one month rest, the maintenance phase consists of:Temozolomide is given orally (30 min after Folinic acid), at 200 mg/m²/day every day during 5 days: one course every month during 6 months (6 maintenance course).
Intervention Type
Drug
Intervention Name(s)
folinic acid at pharmacological dose is the escalated drug
Other Intervention Name(s)
Folinate de Calcium, Lederfoline
Intervention Type
Radiation
Intervention Name(s)
High voltage radiation therapy (linear accelerator)
Intervention Description
Brain tumor field is irradiated Five days a week, during Stupp regimen during 6 weeks. During the sams time, Folinic acid and Temozolomide are given orally every days (six weeks).
Primary Outcome Measure Information:
Title
Maximal Tolerated Dose
Description
maximal tolerated dose 3x3 patients inclusion(modified Fibonnacci dose escalation )
Time Frame
day 43
Secondary Outcome Measure Information:
Title
MGMT gene re-methylation
Description
MGMT gene re-methylation in tumoral and blood samples
Time Frame
day 43
Other Pre-specified Outcome Measures:
Title
Progression-free survival (PFS)
Description
Progression-free survival (PFS)
Time Frame
Year 1
Title
Folic acid and Temozolomide combination Toxicity evaluation
Description
Acute toxicity: Common toxicity criteria version 4.03
Time Frame
day 43

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Operated GBM (complete or near complete resection) Un-methylated MGMT gene Exclusion Criteria: Non operable GBM Methylated MGMT
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mario CAMPONE, MD, PhD
Organizational Affiliation
Institut Cancerologie de l'Ouest
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut de Cacerologie de l'ouest - site Paul Papin
City
Angers
ZIP/Postal Code
49055
Country
France
Facility Name
CHU de Lyon
City
Bron
ZIP/Postal Code
69677
Country
France
Facility Name
ICO site Gauducheau
City
Nantes
ZIP/Postal Code
44805
Country
France
Facility Name
CLCC Antoine Lacassagne
City
Nice
ZIP/Postal Code
06189
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
15758009
Citation
Stupp 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.
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Phase-1 Study of Folinic Acid to Modulate MGMT Gene in Glioblastoma

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