Radiation Therapy Plus Carboplatin and Lobradimil in Treating Children With Newly Diagnosed Brain Stem Gliomas

Children's Oncology Group13 enrolled

Overview

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs such as carboplatin and lobradimil may make the tumor cells more sensitive to radiation therapy. PURPOSE: Phase I trial to study the effectiveness of combining radiation therapy with carboplatin and lobradimil in treating children who have newly diagnosed brain stem gliomas.

OBJECTIVES: * Determine the maximum tolerated duration of lobradimil plus carboplatin with radiotherapy in patients with newly diagnosed brain stem gliomas. * Determine the toxic effects of this treatment regimen in these patients. * Assess the response to radiotherapy in patients treated with this regimen. OUTLINE: Patients receive radiotherapy for 5 consecutive days a week for 6.5 weeks, for a total of 33 doses. Patients receive carboplatin IV over 15 minutes followed by lobradimil IV over 10 minutes concurrently with radiotherapy. The first cohort of 3-6 patients receives treatment with carboplatin and lobradimil for the first three weeks of radiotherapy, with the duration of chemotherapy increasing by one week with each subsequent cohort until the maximum duration of 6.5 weeks is reached or until unacceptable toxicity occurs in 2 of 6 patients. Patients are followed at 6 weeks; every 3 months for 2 years; every 6 months for 3 years; and then annually thereafter. PROJECTED ACCRUAL: A total of 15-24 patients will be accrued for this study within 36 months.

Study Type

INTERVENTIONAL

Purpose

TREATMENT

Enrollment

Conditions

Brain and Central Nervous System Tumors

Interventions

carboplatinDRUG

cereportDRUG

radiation therapyRADIATION

Eligibility

Sex: ALLMin age: 3 YearsMax age: 21 Years

Medical Language ↔ Plain English

DISEASE CHARACTERISTICS: * Newly diagnosed diffuse, intrinsic brain stem gliomas * Measurable disease * No disseminated disease at sites other than brain stem * No neurofibromatosis * Treatment must begin within 31 days of diagnosis * Date of diagnosis will be considered date of surgery in patients undergoing surgical biopsy PATIENT CHARACTERISTICS: Age: * 3 to 21 Performance status: * Karnofsky 50-100% (over 10 years of age) * Lansky 50-100% (10 years of age and under) Life expectancy: * At least 2 months Hematopoietic: * Absolute neutrophil count at least 1,500/mm\^3 * Platelet count at least 100,000/mm\^3 * Hemoglobin at least 10 g/dL Hepatic: * Bilirubin less than 1.5 times upper limit of normal (ULN) * SGPT no greater than 2.5 times ULN (4.0 times ULN with antiepileptic or steroid medications) Renal: * Creatinine less than ULN for age OR * Creatinine clearance or glomerular filtration rate greater than 80 mL/min Other: * No history of severe allergic reaction to any platinum-containing compound * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy * No concurrent growth factors during therapy with carboplatin Chemotherapy * Not specified Endocrine therapy * Prior corticosteroids for brain stem glioma are allowed Radiotherapy * Not specified Surgery * Prior surgery for brain stem glioma is allowed Other * At least 24 hours since any of the following medications: * Vasodilating compounds * Angiotensin-converting enzyme inhibitors * Calcium channel blockers * Beta blockers * No other prior therapy for brain stem glioma

Locations (19)

Children's Hospital Los Angeles

Los Angeles, California, United States

Outcomes

Primary Outcomes

Progression Free Survival

A MRI scan will be performed six (6) weeks after completion of radiation, plus at three-month intervals thereafter for two years, as long as there is no evidence of progressive disease. Children who are progression-free two years after treatment will have MRI scanning at six-month intervals, thereafter, for three more years

Data from ClinicalTrials.gov

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