- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT00516282
VNP40101M and Temozolomide in Treating Patients With Progressive or Relapsed Malignant Glioma
A Phase I/II Trial of Cloretazine® (VNP40101M) and Temodar® (Temozolomide) for Patients With Malignant Glioma in First Relapse or Progression
RATIONALE: Drugs used in chemotherapy, such as temozolomide and VNP40101M, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Temozolomide may also stop the growth of tumor cells by blocking blood flow to the tumor.
PURPOSE: This phase I/II trial is studying the side effects and best dose of VNP40101M when given together with temozolomide and to see how well it works in treating patients with progressive or relapsed malignant glioma.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
OBJECTIVES:
- To determine the maximum tolerated dose (MTD) of VNP40101M when administered with temozolomide in patients with progressive or relapsed (first relapse) malignant glioma. (Phase I)
- To record the toxicities of VNP40101M when administered with temozolomide. (Phase I and II)
- To measure the level of AGT expression in peripheral blood monocytes before treatment with temozolomide and just prior to the administration of VNP40101M. (Phase I and II)
- To determine MGMT methylation status as well as other methylation patterns in blood and tissue from patients treated with this regimen and correlate with outcome. (Phase I and II)
- To determine the 6- and 12-month progression-free survival rates of patients treated with this regimen. (Phase II)
- To determine overall survival of patients treated with this regimen. (Phase II)
- To determine the complete and partial response rates in patients treated with this regimen. (Phase II)
- To determine CSF penetration of VNP40101M once the MTD is reached from phase I and correlate with serum/plasma pharmacokinetics. (Phase II)
OUTLINE:
- Phase I: Patients receive oral temozolomide on days 1-7 and VNP40101M IV over 15-30 minutes 2 hours after the last dose of temozolomide on day 7. Treatment repeats every 7 weeks in the absence of disease progression or unacceptable toxicity.
Cohorts of 3-6 patients receive escalating doses of VNP40101M until the maximum tolerated dose (MTD) is determined The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose limiting toxicity.
- Phase II: Patients receive oral temozolomide and VNP40101M as in phase I. VNP40101M is given at the MTD determined in phase I.
In both phases, patients complete the Functional Assessment of Cancer Therapy-Brain (FACT-BR) questionnaire on day 1 of each course.
Blood is collected for in vitro isolation of mononuclear cells for analysis of O^6 alkylguanine DNA alkyltransferase on days 1 and 7 of course 1. Blood, plasma, CSF, and formalin-fixed paraffin-embedded tissue blocks are collected for gene methylation studies, including MGMT, at baseline and on day 1 of each course.
Type d'étude
Inscription (Réel)
Phase
- La phase 1
Contacts et emplacements
Lieux d'étude
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Illinois
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Chicago, Illinois, États-Unis, 60611-2998
- Hematology-Oncology Associates of Illinois
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Chicago, Illinois, États-Unis, 60611-3013
- Northwestern University
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
DISEASE CHARACTERISTICS:
Inclusion criteria:
Histologically proven malignant glioma including any of the following:
- Glioblastoma multiforme
- Gliosarcoma
- Anaplastic astrocytoma
- Anaplastic oligodendroglioma
- Anaplastic mixed oligoastrocytoma
- Malignant astrocytoma not otherwise specified
- Unequivocal evidence of tumor recurrence or progression by MRI or CT scan with contrast
- No more than one relapse
Patients having undergone recent resection of recurrent or progressive tumor will be eligible as long as all of the following conditions apply:
- More than 2 weeks from surgery and have recovered from the effects of surgery
- Evaluable or measurable disease following resection of recurrent tumor is not mandated for eligibility into the study if a treatment failure can be evaluated
Enhanced CT scan/ MRI should be done no later than 96 hours in the immediate post-operative period or 4-6 weeks post-operatively
- If the 96-hour scan is more than 2 weeks from registration, the scan needs to be repeated
- A baseline scan should be performed within 14 days prior to registration and on a steroid dosage that has been stable for 5 or more days otherwise a new baseline MRI/CT is required
- The same type of scan (i.e., MRI or CT scan) must be used throughout the period of protocol treatment for tumor measurement
- Must have failed prior external-beam radiotherapy
- Must have failed one prior systemic treatment with chemotherapy or biologic agents
PATIENT CHARACTERISTICS:
Inclusion criteria:
- Karnofsky performance status 60-100%
- Life expectancy > 12 weeks
- WBC > 3,000/mm³
- ANC > 1,500/mm³
- Platelet count > 100,000/mm³
- Hemoglobin > 10 mg/dL
- AST and ALT < 4 times upper limit of normal (ULN)
- Bilirubin < 2 times ULN
- Creatinine < 1.5 times ULN
- Fertile patients must use acceptable contraceptive methods (abstinence, intrauterine device [IUD], oral contraceptive or double barrier device)
- Negative pregnancy test
- Not pregnant or nursing
Exclusion criteria:
- Active uncontrolled bleeding
- Active infection of any kind
- Unwilling or unable to follow protocol requirements or to give informed consent
Active heart disease including any of the following:
- Myocardial infarction within the past 3 months
- Uncontrolled arrhythmias
- Uncontrolled coronary artery disease
- Uncontrolled congestive heart failure
- Known HIV-positive patients (HIV testing is not required)
- History of any other cancer (except non-melanoma skin cancer or carcinoma in-situ of the cervix) unless in complete remission and off all therapy for that disease for a minimum of 3 years
PRIOR CONCURRENT THERAPY:
Inclusion criteria:
- See Disease Characteristics
- Recovered from prior therapy
- At least 2 weeks since prior vincristine
- More than 4 weeks since prior cytotoxic therapy (6 weeks for nitrosoureas)
- More than 4 weeks since prior radiotherapy
- More than 4 weeks since prior experimental biologic agents (e.g., EGFR inhibitors, etc)
- More than 3 weeks since prior procarbazine administration
More than 2 weeks since prior non-cytotoxic agents (e.g., interferon, tamoxifen, thalidomide, or isotretinoin)
- Radiosensitizer does not count
At least 2 weeks since prior and no concurrent enzyme inducing anticonvulsants
- If patient is on an enzyme inducing anticonvulsant, they may be converted to a non-enzyme inducing anticonvulsant
Exclusion criteria:
- Any other concurrent standard or investigational treatment for cancer, or any other investigational agent for any indication
- Concurrent disulfiram
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
MTD of CLORETAZINE
Délai: At the end of phase one
|
To determine the MTD of CLORETAZINE when administered with Temodar® in patients with malignant gliomas in first or second relapse
|
At the end of phase one
|
|
Progression-free survival rate
Délai: End of Phase II
|
To determine the 6 and 12 month progression-free survival rate.
|
End of Phase II
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Toxicities of CLORETAZINE when administered with Temodar®.
Délai: Adverse events are monitored at screening/baseline;day one; termination visit; followup until death.
|
To record the toxicities of CLORETAZINE when administered with Temodar®. (Toxicity is assessed continuously through routine medical monitoring of the patient throughout each cycle and all adverse events are recorded cumulatively on the case report forms). |
Adverse events are monitored at screening/baseline;day one; termination visit; followup until death.
|
|
MGMT Methylation Status
Délai: Baseline and day seven of every cycle
|
To determine MGMT methylation status as well as other methylation patterns in blood correlate with outcome.
|
Baseline and day seven of every cycle
|
|
Determine overall survival
Délai: All patients will be followed until death
|
To determine overall survival.
|
All patients will be followed until death
|
|
Response rate to CLORETAZINE after Temodar® in patients with malignant gliomas in first or second relapse
Délai: Day one of every cycle
|
To determine the response rate to CLORETAZINE after Temodar® in patients with malignant gliomas in first or second relapse.
|
Day one of every cycle
|
|
Record the toxicities of CLORETAZINE when administered after Temodar
Délai: Continuously after the first dose;within thirty days of each administration of investigational agent
|
To record the toxicities of CLORETAZINE when administered after Temodar®
|
Continuously after the first dose;within thirty days of each administration of investigational agent
|
|
Measure the level of AGT expression
Délai: Day seven of every cycle
|
To measure the level of AGT expression in peripheral blood monocytes before treatment with Temodar® and just prior to the administration of CLORETAZINE.
|
Day seven of every cycle
|
|
CSF penetration of CLORETAZINE
Délai: Day seven of cycle one of Phase 2 only
|
To determine CSF penetration of CLORETAZINE once the MTD is reached from phase I and correlate with serum/plasma PK
|
Day seven of cycle one of Phase 2 only
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Maladies du système nerveux
- Tumeurs par type histologique
- Tumeurs
- Tumeurs par site
- Tumeurs, glandulaires et épithéliales
- Tumeurs, neuroépithéliales
- Tumeurs neuroectodermiques
- Tumeurs, cellules germinales et embryonnaires
- Tumeurs, tissu nerveux
- Gliome
- Tumeurs du système nerveux
- Tumeurs du système nerveux central
- Mécanismes moléculaires de l'action pharmacologique
- Agents antinéoplasiques
- Agents antinéoplasiques, alkylants
- Agents d'alkylation
- Témozolomide
Autres numéros d'identification d'étude
- NU 07C1
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