Efficacy and Safety of Imatinib Mesylate Plus Hydroxyurea (HU) in Patients With Recurrent Glioblastoma Multiforme (GBM)

NCT ID: NCT00290771

Last Updated: 2011-05-16

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 231 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-02-28
• Study Completion Date: 2008-08-31

Brief Summary

This was an investigational study to assess the objective overall response (OOR) rate (complete response [CR] + partial response [PR]) of imatinib mesylate and hydroxyurea (hydroxycarbamide) combination therapy in patients with recurrent glioblastoma multiforme (brain tumors). This study also evaluated the duration of tumor response (as per MacDonald criteria), clinical benefit, progression-free survival rate at 6 and 12 months, and the survival rate at 12 and 24 months.

Detailed Description

This ClinicalTrials.gov record includes the results from two studies (Novartis protocol IDs CSTI571H2201 and CSTI571H2202) which were conducted separately but reported together in a single clinical study report. Both studies were phase II, open-label, multicenter, single-arm studies that evaluated the efficacy of imatinib mesylate plus hydroxyurea in subjects with progressive glioblastoma multiforme. The studies were identical in design with two exceptions: Patients in study CSTI571H2201 received a dose of imatinib 600 mg once daily and were not allowed concomitant use of enzyme-inducing anticonvulsant drugs (EIACDs); patients in study CSTI571H2202 received a dose of imatinib 500 mg twice daily and were allowed concomitant use of EIACDs.

Conditions

Recurrent Glioblastoma Multiforme (GBM)

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Imatinib 600 mg + hydroxyurea 1000 mg

Patients took imatinib 600 mg (1 imatinib 400 mg tablet and 2 imatinib 100 mg tablets) orally once daily with the morning meal. Patients were instructed to swallow the tablets while drinking a large glass of water. In addition to imatinib, patients took hydroxyurea 500 mg orally twice daily with the morning and evening meals. Patients were not allowed concomitant use of enzyme-inducing anticonvulsant drugs.

Group Type: EXPERIMENTAL

Imatinib tablets

Intervention Type: DRUG

Imatinib was supplied as 100 and 400 mg tablets by Novartis.

Hydroxyurea capsules

Intervention Type: DRUG

Hydroxyurea was supplied locally as 500 mg capsules.

Imatinib 1000 mg + hydroxyurea 1000 mg

Patients took imatinib 500 mg (1 imatinib 400 mg tablet and 1 imatinib 100 mg tablet) orally twice daily with the morning and evening meals. Patients were instructed to swallow the tablets while drinking a large glass of water. In addition to imatinib, patients took hydroxyurea 500 mg orally twice daily with the morning and evening meals. Patients were allowed concomitant use of enzyme-inducing anticonvulsant drugs.

Group Type: EXPERIMENTAL

Imatinib tablets

Intervention Type: DRUG

Imatinib was supplied as 100 and 400 mg tablets by Novartis.

Hydroxyurea capsules

Intervention Type: DRUG

Hydroxyurea was supplied locally as 500 mg capsules.

Interventions

Imatinib tablets

Imatinib was supplied as 100 and 400 mg tablets by Novartis.

Intervention Type: DRUG

Hydroxyurea capsules

Hydroxyurea was supplied locally as 500 mg capsules.

Intervention Type: DRUG

Other Intervention Names

Glivec®

Eligibility Criteria

Inclusion Criteria

• Males and females ≥ 18 years old.
• Histologically-confirmed diagnosis of progressive primary glioblastoma multiforme (GBM) based on original diagnosis. Patients with prior low-grade glioma were eligible if histological re-assessment demonstrated transformation to GBM.
• No more than one prior episode of progressive disease following previously received surgery and/or radiation and only one prior chemotherapy exposure of either temozolomide (TMZ) or nitrosourea including the application of polifeprosan (Gliadel®) wafers.
• Presence of measurable disease on gadolinium-enhanced magnetic resonance imaging (MRI).
• Patients taking steroids must have been on a stable dose for ≥ 7 days.
• Eastern Cooperative Oncology Group (ECOG) performance score ≤ 2.
• Hemoglobin ≥ 10 g/dL (or hematocrit > 29%), absolute neutrophil count (ANC) > 1500 cells/L, platelets > 100,000 cells/L.
• Serum creatinine < 1.5 mg/dL, blood urea nitrogen (BUN) < 25 mg/dL, serum aspartate aminotransferase (AST) and bilirubin < 1.5 x upper limit of normal (ULN).
• Sexually-active male and female patients were required to use double-barrier contraception (oral contraceptive plus barrier contraceptive) or must have undergone clinically documented total hysterectomy, ovariectomy, or tubal ligation.
• Female patients of childbearing potential must have had a negative pregnancy test within 48 hours prior to start of study drug.
• Life expectancy ≥ 8 weeks.
• Signed informed consent by the patient prior to patient entry and any study procedure.

Exclusion Criteria

• Receipt of imatinib or hydroxyurea (HU) prior to study entry or receipt of any investigational agent within the last 6 months.
• Patients who had received a second course of chemotherapy or radiotherapy, unless given as a single localized application of radio surgery.
• In study STI571H2201 only, receipt of enzyme-inducing anticonvulsant drugs (EIACDs), eg, carbamazepine, phenobarbital, phenytoin, fosphenytoin, oxcarbazepine, or primidone. Previous EIACD should have been interrupted 4 weeks prior to study start.
• Grade ≥ 2 peripheral edema or pulmonary or pericardial effusions or ascites of any grade.
• Presence of any uncontrolled systemic infection.
• Patients who were not a minimum of 12 weeks from completion of conventional external beam radiotherapy unless:

1. There was new radiographical enhancement outside the field of radiation, or

2. There was new pathological confirmation of recurrent tumor, or

3. Progressive radiographical enhancement noted on post-radiotherapy/TMZ continue to worsen after an additional course of TMZ.

• Evidence of intra-tumor hemorrhage on pretreatment diagnostic imaging, except for stable post-operative Grade 1 hemorrhage, patients with an excessive risk of an intracranial hemorrhagic event, and patients with history of central nervous system (excluding post-operative Grade 1) or intraocular bleed.
• Patients who had undergone major surgery within 2 weeks prior to study entry or who had not recovered from prior major surgery, patients who had received chemotherapy within 4 weeks prior to study start, or who have not recovered from toxic effects of such therapy.
• Impairment of gastrointestinal function or gastrointestinal disease that could significantly alter the absorption of imatinib.
• Patients taking warfarin sodium.
• Known history of human immunodeficiency virus (HIV) seropositivity; testing for HIV was not required at study entry.
• For the purposes of MRI, patients with a pacemaker, ferromagnetic metal implants other than those approved as safe for use in MR scanners (eg, some types of aneurysm clips, shrapnel), patients suffering from uncontrollable claustrophobia, or those physically unable to fit into the machine (eg, obesity).
• Patients considered by the investigator as unlikely to be compliant with the study, take the study medications, travel for the necessary assessment visits, or have other medical conditions likely to interfere with the study assessments.
• Patients with another primary malignancy treated within the prior 3 years except excised squamous cell carcinomas of the skin and carcinoma in situ lesions of other organs which had been treated for cure.
• Patients not able to provide reliable informed consent and who did not have a legal representative for healthcare decisions on their behalf.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Novartis

INDUSTRY

Sponsor Role: lead

Responsible Party

Novartis

Principal Investigators

David Reardon, Dr.

Role: PRINCIPAL_INVESTIGATOR

Duke University

Locations

Duke University Medical Center

Durham, North Carolina, United States

Countries

United States

Other Identifiers

CSTI571H2202

Identifier Type: OTHER

Identifier Source: secondary_id

CSTI571H2201

Identifier Type: -

Identifier Source: org_study_id

NCT00292149

Identifier Type: -

Identifier Source: nct_alias