Metronomic Temozolamide in Patients With Recurrent Glioblastoma

Glioblastoma Clinical Trial

Official title:

PHASE I-II TRIAL OF METRONOMIC TEMOZOLAMIDE WITH INTERMITTENT INTENSIFICATION AND IRINOTECAN IN PATIENTS WITH RECURRENT GLIOBLASTOMA

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01308632
• Other study ID #: GENOM-007
• Status: Active, not recruiting
• Phase: Phase 2/Phase 3
• First received: January 24, 2011
• Last updated: March 2, 2011
• Start date: November 2007
• Est. completion date: June 2012

Study information

• Verified date: March 2011
• Source: Grupo Español de Investigación en Neurooncología
• Contact: n/a
• Is FDA regulated: No
• Health authority: Spain: Spanish Agency of Medicines
• Study type: Interventional

Clinical Trial Summary

Indication:

Subjects with glioblastoma at first relapse after surgery, radiotherapy and first-line temozolomide (TMZ).

Objectives:

1. Phase I endpoint:

• To determine the maximum tolerated dose (MTD) of CPT-11 administered on days 8 and 22 in combination with a fixed, continuous, and metronomic regimen of TMZ, given in 28-day cycles.

2. Phase II endpoints:

Primary endpoint: Progression-free survival at 6 months. Secondary endpoints: Response rate, toxicity profile, overall survival.

Complementary studies:

To assess the effect of treatment on plasma concentration of thrombospondin-1 (TSP1), soluble VEGF receptor 1 (sVEGF-1) and VEGF-A, and their correlation with clinical outcome.

• To assess the correlation between immunohistochemical expression of PTEN and MGMT proteins, and clinical outcomes.

Description:

Study Design: Open label, phase I - II trial. Phase I trial: TMZ will be administered in a fixed schedule as follows:

TMZ

• 50 mg/m2/day divided in three daily doses (approx. 17 mg/m2/8 hours) on days 1-7, 9-21, and 23-28.

• 100 mg/m2 in a morning single dose on days 8 and 22

CPT-11 starting dose:

.100 mg/m2 on days 8 and 22, administered 3 to 6 hours after TMZ.(Level 1).One cycle = 28 days. CPT-11 will be escalated in successive cohorts of 3 patients as follows: 115, 130, 145, 160 mg/m2 .

Three patients will be treated at dose level 1. If there is no DLT, 3 new patients will be treated at dose level 2, and so on. If 1 or 2 of the 3 patients initially recruited at each treatment level experience DLT, 3 additional patients will be included at the same level. If DLT is registered in less than 3 of the 6 patients treated at this level, 3 new patients will be included in the next dose level. If 3 or more of the 6 patients experience DLT, the phase I trial will be closed and the previous treatment level will be chosen for the phase II trial. If all 3 initial patients at one level experience DLT, the previous dose level will be used in the phase II trial.

If DLT is found at dose level 1, phase I trial will be re-started at level -2 (70 mg/m2 ) and -1 (85 mg/m2).

Definition of DLT:

• Absolute neutrophil count (ANC) < 500/ μl > 7 days

• Platelet count < 25000/ μl

• A delay in starting a new cycle by > 7 days to allow recovery from toxicity (ANC ≥ 1500/ μl and platelet count ≥ 100000/ μl

• Febrile Neutropenia

• Non-haematological toxicity grade 3-4, except alopecia and nausea/vomiting or diarrhea without adequate prophylaxis or treatment.

Phase II trial: Patients will receive the treatment schedule at the dose level stated in the phase I study. Treatment will be maintained until progression or excessive toxicity.

Patient evaluation: A physical examination, blood count, and basic biochemistry assessment will be performed within 3 weeks before treatment and at each study visit. Tumor recurrence or progression has to be demonstrated by MRI scan performed within 3 weeks before the first treatment course and after every second course of chemotherapy. The assessment of tumor response will be based on criteria defined by Macdonald et al. Study visits will be performed on days 1, 8, 15 and 22 of first and second treatment course, and on days 8 and 22 thereafter, if no significant toxicity has been observed.

Complementary studies: The immunohistochemical expression of PTEN and MGMT will be assessed in paraffin sections of tumor tissue of all patients.

Blood samples for enzyme immunoassay of TSP1, sVEGFR-1 and VEGF-A will be collected within 3 weeks before treatment, after course 1 and every 3 treatment courses thereafter.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 30
• Est. completion date: June 2012
• Est. primary completion date: June 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients > 18 years old

2. Histological confirmed GB at first relapse, assessed by MRI scan, after surgical resection or biopsy, radiotherapy, and first-line chemotherapy with TMZ. A TMZ treatment duration of at least 3 months is required. Previous chemotherapy with CPT-11 is not allowed.

3. Karnofsky performance status = 70.

4. ANC = 1500/ µl, platelet count = 100000/ µl, haemoglobin > 10 g/dl, serum creatinine and total bilirubin < 1.5 times the upper limit of laboratory normal, transaminases < 3.0 times the upper limit of laboratory normal.

5. Stable or descending corticosteroid dose = 72 hours before baseline MRI and study treatment.

6. Life expectancy greater than 3 months

7. Written informed consent.

Exclusion Criteria:

1. Pregnancy or breastfeeding.

2. Neurological impairment that precludes comprehension or treatment administration

3. Vomiting or other condition that interfere with oral administration of TMZ

4. Previous or concurrent malignancy, excluding basal cell carcinomas or in situ cervical cancer.

5. Concurrent disease that could interfere with treatment

6. Concurrent treatment with enzyme-inducing drugs. Patients under enzyme-inducing anticonvulsants should discontinue treatment at least one week before study treatment and begin a new anti-epileptic treatment with non enzyme-inducing drugs if indicated.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Glioblastoma

Intervention

Drug:
• Temozolamide, irinotecan
Phase I trial: TMZ will be administered in a fixed schedule as follows: TMZ 50 mg/m2/day divided in three daily doses (approx. 17 mg/m2/8 hours) on days 1-7, 9-21, and 23-28. 100 mg/m2 in a morning single dose on days 8 and 22 CPT-11 starting dose: 100 mg/m2 on days 8 and 22, administered 3 to 6 hours after TMZ. (Level 1) One cycle = 28 days CPT-11 will be escalated in successive cohorts of 3 patients as follows: 115, 130, 145, 160 mg/m2 .

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Grupo Español de Investigación en Neurooncología

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Efficacy of the treatment (Phase I)	To determine the maximum tolerated dose (MTD) of CPT-11 administered on days 8 and 22 in combination with a fixed, continuous and metronomic regimen of TMZ, given in 28-days cycles to use the Recommended Dose in phase II	every patient should receive at least one cycle ( 28 days)	Yes
Primary	Progression-free survival (Phase II)	The time the patient is not in progression, since the beginning of the treatment	Since the initial of the treatment until the patient progression	No
Secondary	Assess the toxicity of the treatment	Toxicity Profile (in phase II)	the patients will be followed until disease progression	Yes
Secondary	Progression-free survival at 6 months	Progression-free survival at 6 months (Phase I)	6 months since the pacient is included in the trial	No
Secondary	overall survival		the patients will be followed until death	No