Combination Chemotherapy and Radiation Therapy With or Without Methotrexate in Treating Young Patients With Newly Diagnosed Gliomas

NCT ID: NCT00278278

Last Updated: 2013-12-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE3

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2003-09-30

Brief Summary

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RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Radiation therapy uses high-energy x-rays to kill tumor cells. It is not yet known whether giving methotrexate together with combination chemotherapy and radiation therapy is more effective than combination chemotherapy and radiation therapy alone in treating gliomas.

PURPOSE: This randomized phase III trial is studying giving methotrexate together with combination chemotherapy and radiation therapy to see how well it works compared to combination chemotherapy and radiation therapy alone in treating young patients with newly diagnosed gliomas.

Detailed Description

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OBJECTIVES:

Primary

* Determine if the addition of high-dose methotrexate prior to standard treatment improves survival of patients with malignant high-grade glioma or diffuse intrinsic pontine glioma as compared to standard treatment only.

Secondary

* Determine if the addition of high-dose methotrexate, as compared to standard treatment only, improves the tumor response of these patients.
* Determine if high-dose methotrexate, compared to standard treatment only, improves the progression-free or event-free survival of these patients.
* Determine if high-dose methotrexate, as compared to standard treatment only, improves the health status (quality of life) of these patients.
* Determine if consolidation therapy improves the overall, progression-free, or event-free survival rates as compared to the historical control group.

OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to tumor location includes pons (yes vs no) and complete or nearly complete resection (yes vs no).

* Surgery: All patients are encouraged to undergo radical resection of the tumor to reduce intracranial pressure, remove as much tumor tissue as possible, and obtain tumor tissue for histological diagnosis. Within 14 days after surgery, patients proceed to induction chemotherapy.
* Induction therapy: Patients are randomized to 1 of 2 treatment arms.

* Arm I:

* High-dose methotrexate with leucovorin calcium: Patients receive high-dose methotrexate IV over 24 hours on days 1 and 15 and leucovorin calcium IV every 6 hours on days 2-3 an 16-17. Patients proceed to chemoradiotherapy 4 weeks later.
* Chemoradiotherapy (course 1): Patients undergo external beam radiotherapy once daily, 5 days a week, for approximately 6 weeks. Beginning on the first day of radiotherapy, patients receive cisplatin IV over 1 hour on days 1-5, etoposide IV over 2 hours on days 1-3, and vincristine IV on days 5, 12, 19, 26, and 33. Patients proceed to course 2 of chemoradiotherapy 7 days prior to completion of radiotherapy.
* Chemoradiotherapy (course 2): Patients receive ifosfamide IV over 1 hour and cisplatin IV over 1 hour on days 1-5, etoposide IV over 2 hours on days 1-3, and vincristine IV on day 5. Patients proceed to consolidation chemotherapy 4 weeks later.
* Arm II: Patients receive chemoradiotherapy courses 1 and 2 as in arm I and proceed to consolidation chemotherapy 4 weeks later.
* Consolidation chemotherapy: Patients receive vincristine IV on days 1, 8, and 15, oral lomustine once on day 2, and oral prednisone once daily on days 1-17. Treatment repeats every 6 weeks for up to 8 courses.

Quality of life is assessed 1 week after surgery, after completion of chemoradiotherapy, at 1, 4, and 13 months after completion of consolidation chemotherapy, and then annually for 3 years.

After completion of study treatment, patients are followed periodically for 3 years.

PROJECTED ACCRUAL: A total of 150 patients will be accrued for this study.

Conditions

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Brain and Central Nervous System Tumors

Keywords

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untreated childhood brain stem glioma untreated childhood cerebellar astrocytoma childhood high-grade cerebral astrocytoma childhood spinal cord neoplasm

Study Design

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Allocation Method

RANDOMIZED

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Arm I

Patients receive high-dose methotrexate IV over 24 hours on days 1 and 15 and leucovorin calcium IV every 6 hours on days 2-3 an 16-17. Four weeks later, patients undergo external beam radiotherapy once daily, 5 days a week, for approximately 6 weeks.

Beginning on the first day of radiotherapy, patients receive cisplatin IV over 1 hour on days 1-5, etoposide IV over 2 hours on days 1-3, and vincristine IV on days 5, 12, 19, 26, and 33. Beginning seven days prior to completion of radiotherapy, patients receive ifosfamide IV over 1 hour and cisplatin IV over 1 hour on days 1-5, etoposide IV over 2 hours on days 1-3, and vincristine IV on day 5.

Group Type EXPERIMENTAL

cisplatin

Intervention Type DRUG

Given IV

etoposide

Intervention Type DRUG

Given IV

ifosfamide

Intervention Type DRUG

Given IV

lomustine

Intervention Type DRUG

Given IV

methotrexate

Intervention Type DRUG

Given IV

prednisone

Intervention Type DRUG

Given IV

vincristine sulfate

Intervention Type DRUG

Given IV

Arm II

Patients undergo external beam radiotherapy once daily, 5 days a week, for approximately 6 weeks.

Beginning on the first day of radiotherapy, patients receive cisplatin IV over 1 hour on days 1-5, etoposide IV over 2 hours on days 1-3, and vincristine IV on days 5, 12, 19, 26, and 33. Beginning seven days prior to completion of radiotherapy, patients receive ifosfamide IV over 1 hour and cisplatin IV over 1 hour on days 1-5, etoposide IV over 2 hours on days 1-3, and vincristine IV on day 5.

Group Type ACTIVE_COMPARATOR

cisplatin

Intervention Type DRUG

Given IV

etoposide

Intervention Type DRUG

Given IV

ifosfamide

Intervention Type DRUG

Given IV

lomustine

Intervention Type DRUG

Given IV

prednisone

Intervention Type DRUG

Given IV

vincristine sulfate

Intervention Type DRUG

Given IV

Interventions

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cisplatin

Given IV

Intervention Type DRUG

etoposide

Given IV

Intervention Type DRUG

ifosfamide

Given IV

Intervention Type DRUG

lomustine

Given IV

Intervention Type DRUG

methotrexate

Given IV

Intervention Type DRUG

prednisone

Given IV

Intervention Type DRUG

vincristine sulfate

Given IV

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

DISEASE CHARACTERISTICS:

* Newly diagnosed tumors of the brain or spinal cord, meeting one of the following criteria:

* Histologically\* confirmed diagnosis of 1 of the following high-grade gliomas:

* Glioblastoma (WHOº IV)
* Anaplastic astrocytoma (WHOº III)
* Gliosarcoma (WHOº III or IV)
* Anaplastic oligo-astrocytoma NOTE: \*Histological requirement may be waived for other types of brainstem glioma
* Radiologically proven diffuse intrinsic pontine glioma
* Second malignancy or disseminate metastases or multifocal tumors are allowed if the field of irradiation is not too large

* No diffuse metastases making craniospinal irradiation necessary

PATIENT CHARACTERISTICS:

* No cardiorespiratory insufficiency requiring medical respiration
* No low blood pressure requiring systemic catecholamines
* No severe neurological damage (e.g., coma)
* No tetraplegia without possibility to communicate
* No other poor clinical condition
* Not pregnant
* Fertile patients must use effective contraception
* No hypersensitivity to methotrexate, cisplatin, vincristine, lomustine, or ifosfamide
* No other malignancy preceding radiotherapy that does not allow further radiation

PRIOR CONCURRENT THERAPY:

* No prior chemotherapy for brain tumor
* The following prior therapies are allowed:

* Mistletoe
* H15 (extract of Boswellia serrata)
* Homeopathy therapy with dilution \> 4D
* Alternative medicine without proven efficacy
* No prior radiotherapy for brain tumor
* No concurrent alcohol or tobacco consumption
* No concurrent participation in another study
Minimum Eligible Age

3 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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German Society for Pediatric Oncology and Hematology GPOH gGmbH

OTHER

Sponsor Role lead

Responsible Party

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University Children's Hospital

Principal Investigators

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Christoph Kramm, MD

Role: STUDY_CHAIR

University Children's Hospital

Locations

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M. D. Anderson Cancer Center at University of Texas

Houston, Texas, United States

Site Status

Countries

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United States

References

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Wolff JE, Kortmann RD, Wolff B, Pietsch T, Peters O, Schmid HJ, Rutkowski S, Warmuth-Metz M, Kramm C. High dose methotrexate for pediatric high grade glioma: results of the HIT-GBM-D pilot study. J Neurooncol. 2011 May;102(3):433-42. doi: 10.1007/s11060-010-0334-2. Epub 2010 Aug 8.

Reference Type RESULT
PMID: 20694800 (View on PubMed)

Other Identifiers

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GPOH-HIT-GBM-D

Identifier Type: -

Identifier Source: secondary_id

EU-205100

Identifier Type: -

Identifier Source: secondary_id

CDR0000454723

Identifier Type: -

Identifier Source: org_study_id