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Impact of the Platelet Level in Patients Treated for Glioblastoma With Temozolomid (GLIOPLAK)

Primary Purpose

Glioblastoma

Status
Active
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Platelet level determination
Sponsored by
Centre Henri Becquerel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Glioblastoma focused on measuring Stupp protocol, glioblastoma, thrombocytopenia

Eligibility Criteria

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

Inclusion Criteria:

  • Age Superior to 18 years
  • Inform consent form signed
  • Newly diagnosed (histologically) glioblastoma
  • Stupp protocol treatment
  • with social insurance

Exclusion Criteria:

  • Not inform consent form signed
  • participation to another clinical trial
  • other cancer
  • background of hematological pathology
  • patient under guardianship, curatorship

Sites / Locations

  • Centre Henri Becquerel

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Stupp protocol

Arm Description

Blood assessment of the platelet level every week during the radiotherapy phase and every cycle during the chemotherapy

Outcomes

Primary Outcome Measures

Number of time where platelet level was Under 100 000 per mm3
Determination of platelet level to predict the risk of thrombocytopenia

Secondary Outcome Measures

Overall survival
time between inclusion and death
Therapeutic modifications
Proportion of patient with treatment modifications

Full Information

First Posted
November 16, 2015
Last Updated
May 2, 2023
Sponsor
Centre Henri Becquerel
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1. Study Identification

Unique Protocol Identification Number
NCT02617745
Brief Title
Impact of the Platelet Level in Patients Treated for Glioblastoma With Temozolomid
Acronym
GLIOPLAK
Official Title
Impact of the Platelet Level During Radiotherapy Associated With Temozolomide in Patients Treated for Glioblastoma
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 30, 2015 (Actual)
Primary Completion Date
November 28, 2022 (Actual)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Henri Becquerel

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of GLIOPLAK is to evaluate the predictive value of a biological test performed in the radio-chemotherapy phase in patients suffering from glioblastoma. The studied parameter is the variation in platelet count during the radio-chemotherapy phase. The main objective is to identify early in Stupp protocol a group of patients having high risk to undergo thrombocytopenia in maintenance phase of temozolomide. With this result an algorithm of platelet monitoring for patients treated with Stupp protocol wil be proposed.
Detailed Description
Glioblastoma is the most common primitive cerebral tumor. Currently its optimal treatment is based on a multidisciplinary approach combining an initial surgical resection, if feasible, then Stupp protocol. Stupp protocol consists of two phases: first phase involves external radiotherapy with concomitant oral temozolomide at a dose of 75mg/m2 per day for about six weeks. After 4 weeks of therapy break, maintenance phase begins with temozolomide alone, for a period of 6 cycles (1 cycle = 5 days over 28). The dose of temozolomide is 150mg/m2 on the first cycle followed by 200 mg/m2. One major limiting toxicity of temozolomide is hematologic, especially thrombocytopenia. They occur in around 15 and 20% of patients in maintenance phase. Thrombocytopenia has an impact on the schedule of Stupp protocol such as dose reduction or even early discontinuation. Currently no predictive marker of thrombocytopenia in the maintenance phase was identified. Such marker could be of major interest to adapt biological and clinical follow-up by patient in maintenance phase. We conduct a retrospective analysis on a cohort of patients suffering from glioblastoma and treated with Stupp protocol. We found that a decrease in platelet count during the radio-chemotherapy phase could be highly predictive of protocol changes in maintenance phase of temozolomide due to thrombocytopenia. The main objective of GLIOPLAK is to prospectively confirm the predictive value of this test and to evaluate the prognostic impact of the occurrence of thrombocytopenia <100,000/mm3. Secondary objective of GLIOPLAK are to describe all limiting toxicities in maintenance phase, to constitute a prospective biological collection and to collect biological samples to perform pharmacological analysis (pharmacogenomics and pharmacokinetics parameters).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma
Keywords
Stupp protocol, glioblastoma, thrombocytopenia

7. Study Design

Primary Purpose
Other
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
244 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Stupp protocol
Arm Type
Experimental
Arm Description
Blood assessment of the platelet level every week during the radiotherapy phase and every cycle during the chemotherapy
Intervention Type
Other
Intervention Name(s)
Platelet level determination
Intervention Description
evaluate the predictive value of a biological test performed in the radio-chemotherapy phase in patients suffering from glioblastoma. For this the platelet level will be determined each wek during the radiotherapy phase and each cycle during the chemotherapy phase
Primary Outcome Measure Information:
Title
Number of time where platelet level was Under 100 000 per mm3
Description
Determination of platelet level to predict the risk of thrombocytopenia
Time Frame
one year and 6 months
Secondary Outcome Measure Information:
Title
Overall survival
Description
time between inclusion and death
Time Frame
3 years
Title
Therapeutic modifications
Description
Proportion of patient with treatment modifications
Time Frame
one year and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age Superior to 18 years Inform consent form signed Newly diagnosed (histologically) glioblastoma Stupp protocol treatment with social insurance Exclusion Criteria: Not inform consent form signed participation to another clinical trial other cancer background of hematological pathology patient under guardianship, curatorship
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frederic Di Fiore, MD, PhD
Organizational Affiliation
Centre Henri Becquerel
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Henri Becquerel
City
Rouen
ZIP/Postal Code
76038
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
33148330
Citation
Fontanilles M, Marguet F, Beaussire L, Magne N, Pepin LF, Alexandru C, Tennevet I, Hanzen C, Langlois O, Jardin F, Laquerriere A, Sarafan-Vasseur N, Di Fiore F, Clatot F. Cell-free DNA and circulating TERT promoter mutation for disease monitoring in newly-diagnosed glioblastoma. Acta Neuropathol Commun. 2020 Nov 4;8(1):179. doi: 10.1186/s40478-020-01057-7.
Results Reference
derived

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Impact of the Platelet Level in Patients Treated for Glioblastoma With Temozolomid

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