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Safety of Fluvastatin-Celebrex Association in Low-grade and High Grade Optico-chiasmatic Gliomas (FLUVABREX)

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ClinicalTrials.gov Identifier: NCT02115074
Recruitment Status : Active, not recruiting
First Posted : April 15, 2014
Last Update Posted : January 1, 2019
Sponsor:
Collaborator:
Anticancer Fund, Belgium
Information provided by (Responsible Party):
Centre Oscar Lambret

Brief Summary:

Optico-chiasmatic gliomas have therapeutic feature since surgical resection plays a secondary role. Unlike other sites, many of these tumors are not amenable to complete resection either because of anatomical location, and sometimes they only can be biopsied. A substantial number of children will have recurrences following resection or will experience progression following incomplete tumor removal or biopsy.

Celebrex is a Cox-2 inhibitor with anti-angiogenic and anti-tumor properties, while statins are known to increase the sensitivity of gliomas to anti-tumor agents. Their association could be administered for long periods, in the hope of much reduced risk of toxicities.

This is a national, multicentric, interventional, open-label, non-comparative, and non-randomized phase I study evaluating the maximum tolerated dose of the Fluvastatin in combination with fixed-dose of Celebrex.

This project involves 10 SFCE health centers accustomed to phase I / II studies(Société Française de Lutte contre les Cancers et Leucémies de l'Enfant et de l'Adolescent - French Society for the Fight against Cancer and Leukemia in Children and Adolescents).


Condition or disease Intervention/treatment Phase
Glioma Drug: Fluvastatine Drug: Celebrex Phase 1

Detailed Description:

Dose escalation scheme only concerns Fluvastatin, and is based on a CRML model (Continual Reassessment Method Lilelihood approach). Dose associated with a probability of DLT closest to 25% will be considered as Recommended Phase 2 Dose (RP2D).

Escalation phase :

Patients will be included by cohort of 2. First patient will be included at the first dose level of Fluvastatin (2mg/kg/day). The second patient will be included only after sufficient time to assess the absence of DLT on first patient. In absence of DLT during the first 28-day cycle, dose escalation will be allowed (4, then 6 and 8 mg/kg/day of Fluvastatin).

The second and all subsequent patients will be treated at the dose level which DLT probability is closest to 25%, without skipping step. Intra-patient dose escalation is not allowed. Treatment will be administered until progression, or unacceptable toxicity for one year. A minimum of 21 patients will be included during the 1st step, including a minimum of 6 patients receiving RP2D.

Expansion phase :

At RP2D, the number of subjects will be increased to reach a total of 14 evaluable patients, in order to better characterize RP2D safety. Patients will be included in the expansion phase according CRML model as well, to confirm the recommended dose.

Probabilities of DLT associated with each dose level will be re-estimated by CRML progressively, without the need to suspend inclusions. Results could modify RP2D retained during 1st step (dose reduction or a dose re-escalation).


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 21 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase I Study of Fluvastatin-Celebrex Association for Optico-chiasmatic Low Grade Gliomas and High Grade Gliomas Localized Outside the Brainstem, Relapsed or Refactory, in Children or Young Adults
Actual Study Start Date : June 2014
Actual Primary Completion Date : November 2018
Estimated Study Completion Date : October 2022

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Fluvastatine Celebrex
dose escalation for Fluvastatine
Drug: Fluvastatine

Escalation dose : Level 1: 2mg/kg/day. Level 2: 4mg/kg/day. Level 3: 6mg/kg/day. Level 4: 8mg/kg/day.

Per os from D1 to D14 of each 28 day cycle.

Number of Cycles: until progression or unacceptable toxicity develops.


Drug: Celebrex

Dose levels : 100 mg twice a day (< 20 kg), 200 mg twice a day (20-50 kg), 400 mg twice a day (> 50 kg)

Per os from D1 to D28 of each 28 day cycle.

Number of Cycles: until progression or unacceptable toxicity develops.

Other Name: Celecoxib




Primary Outcome Measures :
  1. Maximum tolerated dose (MTD) of Fluvastatine combined to a fixed-dose of Celebrex [ Time Frame: 28 days (at the end of the first cycle) ]

    The MTD is evaluated according to NCI-CTC v4.0 scale, and is defined as follows:

    • grade 3 or 4 neutropenia leading to a delay of therapy superior to 7 days
    • grade 3 or 4 thrombocytopenia requiring transfusions over a period superior to 7 days
    • grade 3 or 4 non-hematologic toxicities, excepted the following events:

      • nausea and vomiting despite appropriate symptomatic treatment,
      • grade 3 fever, and grade 3 liver toxicity but rapidly reversible,
      • grade 3 elevation of creatine phosphokinase (CPK) levels, but rapidly reversible (back <3 X normal within 2 weeks after interruption of treatment)
    • Toxicity leading to dose reduction (<75% dose protocol) will also be considered as a DLT, although the grade of toxicity does not in itself justify this classification


Secondary Outcome Measures :
  1. Adverse events [ Time Frame: During all the treatment period, for up to 1 year ]
    Safety is assessed according to NCI-CTC v4.0 scale

  2. Efficacy in terms of overall survival [ Time Frame: From date of registration until the date of death from any cause, assessed up to 2 years ]
    Efficacy is measured according to RANO criteria

  3. Efficacy in terms of progression-free survival [ Time Frame: After 3, 6, 9 and 12 months of treatment ]
    Efficacy is measured according to RANO criteria.

  4. Potential interactions between the two drugs [ Time Frame: Pharmacokinetics: 1 blood sample of 1.5 ml is collected during cycle 1 and at day 1 of the second cycle before fluvastatine and celebrex administration. ]

    The Fluvastatin and Celebrex are dosed on the same sample, then compared with pharmacokinetics data from the literature (when drugs are administered alone). The objective is to explore the interaction between the 2 drugs.

    Pharmacokinetic analysis is performed by liquid chromatography coupled to mass spectrometry (LC/MS), with UV detection.


  5. Best response' s distribution during the treatment [ Time Frame: After 3, 6, 9 and 12 months of treatment ]
    Best response is measured according to RANO criteria.



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Ages Eligible for Study:   6 Years to 21 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Histologically confirmed recurrent or progressive primary hypothalamic-chiasmatic low grade glioma, and not warranting a biopsy or surgery
  • Histologically confirmed recurrent or progressive primary hypothalamic-chiasmatic high grade glioma, or in complete remission after a new exeresis, excepted brainstem gliomas
  • Relapsed or refractory disease after at least 1 line adjuvant treatment including radiation therapy, but not surgery
  • Measurable lesions according to RANO criteria for the patients with low grade glioma and for the patients with high grade glioma included in RP2D level (Recommended Phase 2 Dose).
  • Non-measurable lesions according to RANO criteria for patients with high grade glioma included in the dose escalation step.
  • Age > 6 years and < 21 years old
  • Lansky score > 70 or WHO score < 2 (neurological conditions associated with the disease should not be taken into consideration)
  • Haematological conditions: ANC > 1000/mm3 and platelets > 75000/mm3
  • Creatinine < 1.5 x normal for age or calculated clearance > 70 ml/mn/1.73m2
  • Hepatic function: Total bilirubin < 3 N and SGOT and SGPT < 4 N
  • Muscle enzymes : CPK < 2 N
  • No organ toxicity superior to grade 2 according to NCI-CTCAE v4.0
  • No allergy, hypersensibility to one of the compounds of the treatment
  • Patients able to swallow capsules
  • Life expectancy at least > 6 months for low grade gliomas and > 3 months for high grade gliomas
  • Patient affiliated with a health insurance system
  • Effective contraception for patients (male and female) with reproductive potential throughout the treatment period
  • Written informed consent of patient and/or parents/guardians prior to the study participation

Exclusion Criteria:

  • Chemotherapy within 21 days before D1 of experimental treatment. This period may be shortened in case of previous chemotherapy with vincristine (2 weeks), or extended in case of targeted therapies (4 weeks), or treatment by nitrosoureas (6 weeks)
  • Radiotherapy within 6 months before D1 of experimental treatment
  • Peptic ulcer disease, or gastrointestinal bleeding
  • Known hypersensitivity to sulfonamides.
  • History of asthma, acute rhinitis, nasal polyps, angioedema, urticaria or other allergic-type reactions induced by acetylsalicylic acid or NSAIDs , including COX-2 inhibitors (cyclo-oxygenase- 2)
  • Inflammatory bowel disease.
  • Known congestive heart failure (NYHA II- IV)
  • Ischemic proven, peripheral and/or history of arterial stroke (including transient ischemic attack)
  • Pregnancy or breast feeding woman
  • Known allergy to experimental treatment
  • Organ toxicity superior to grade 2 according to NCI-CTCAE v4.0
  • Active infection
  • Pre-existing muscle pathology
  • Unsuitable for medical follow-up (geographic, social or mental reasons)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02115074


Locations
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France
CHU Angers
Angers, France, 49933
Centre Hospitalier de Bordeaux - Hôpital des Enfants
Bordeaux, France, 33076
Centre Oscar Lambret
Lille, France, 59020
Centre Léon Bérard
Lyon, France, 69373
Hôpital pour enfants La Timone
Marseille, France, 13385
Centre Hospitalier de Nantes - Hôpital Mère enfants
Nantes, France, 44000
Institut Curie
Paris, France, 75005
Centre Hospitalier de Strasbourg
Strasbourg, France, 67098
Centre Hospitalier de Purpan - Hôpital des Enfants
Toulouse, France, 31026
Centre Hospitalier de Nancy
Vandoeuvre-les-Nancy, France, 54511
Institut Gustave Roussy
Villejuif, France, 94805
Sponsors and Collaborators
Centre Oscar Lambret
Anticancer Fund, Belgium
Investigators
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Study Director: Pierre LEBLOND, MD Centre Oscar Lambret, Lille, France
Study Director: Nicolas ANDRE, MD Hôpital pour Enfants de " La Timone " AP-HM, Marseille, France

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Responsible Party: Centre Oscar Lambret
ClinicalTrials.gov Identifier: NCT02115074     History of Changes
Other Study ID Numbers: FLUVABREX-1208
First Posted: April 15, 2014    Key Record Dates
Last Update Posted: January 1, 2019
Last Verified: December 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Centre Oscar Lambret:
Low-grade gliomas
high-grade gliomas
optico-chiasmatic
relapsed
refractory
Additional relevant MeSH terms:
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Celecoxib
Glioma
Neoplasms, Neuroepithelial
Neuroectodermal Tumors
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
Neoplasms
Neoplasms, Glandular and Epithelial
Neoplasms, Nerve Tissue
Anti-Inflammatory Agents, Non-Steroidal
Analgesics, Non-Narcotic
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Anti-Inflammatory Agents
Antirheumatic Agents
Cyclooxygenase 2 Inhibitors
Cyclooxygenase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action