Brain and Central Nervous System Tumors

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Radiation Therapy, Arsenic Trioxide, and Temozolomide in Treating Patients With Newly Diagnosed High-Grade Glioma

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as arsenic trioxide and temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Arsenic trioxide and temozolomide may also make tumor cells more sensitive to radiation therapy. Giving radiation therapy together with combination chemotherapy may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of arsenic trioxide when given together with temozolomide and radiation therapy in treating patients with newly diagnosed high-grade glioma.

Background information
Other unique IDs: 
CDR0000600335
CHNMC-07058
CEPHALON-CHNMC-07058

Bevacizumab and Erlotinib After Radiation Therapy and Temozolomide in Treating Patients With Newly Diagnosed Glioblastoma Multiforme or Gliosarcoma

RATIONALE: Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Erlotinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving bevacizumab together with erlotinib may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving bevacizumab together with erlotinib works after radiation therapy and temozolomide in treating patients with newly diagnosed glioblastoma multiforme or gliosarcoma.

Background information
Other unique IDs: 
CDR0000598539
NU-07C3
GENENTECH-NU 07C3
NU-IRB-STU00002792

Sodium Thiosulfate in Preventing Hearing Loss in Young Patients Receiving Cisplatin for Newly Diagnosed Germ Cell Tumor, Hepatoblastoma, Medulloblastoma, Neuroblastoma, or Osteosarcoma

Trial phase: 
Phase III
Recruitment status: 
Recruiting

RATIONALE: Sodium thiosulfate may reduce or prevent hearing loss in young patients receiving cisplatin for cancer. It is not yet known whether sodium thiosulfate is more effective than no additional treatment in preventing hearing loss. PURPOSE: This randomized phase III trial is studying sodium thiosulfate to see how well it works compared with no additional treatment in preventing hearing loss in young patients receiving cisplatin for newly diagnosed germ cell tumor, hepatoblastoma, medulloblastoma, neuroblastoma, or osteosarcoma.

Background information
Trial ID: 
NCT00716976
Other unique IDs: 
CDR0000588655
COG-ACCL0431
Official title: 

A Randomized Phase III Study of Sodium Thiosulfate for the Prevention of Cisplatin-Induced Ototoxicity in Children

Detailed description: 

OBJECTIVES: Primary

  • To compare the efficacy of sodium thiosulfate vs observation in preventing hearing loss in young patients receiving cisplatin for the treatment of newly diagnosed germ cell tumor, hepatoblastoma, medulloblastoma, neuroblastoma, or osteosarcoma.

Number to be enrolled: 
120 patients

Sunitinib in Treating Patients With Recurrent Malignant Glioma

RATIONALE: Sunitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. PURPOSE: This phase II trial is studying how well sunitinib works in treating patients with recurrent malignant glioma.

Background information
Other unique IDs: 
CDR0000599821
NCI-08-C-0168
NCI-P07336

Studying Changes Over Time in Patients With Neurofibromatosis Type 1 and Their Healthy Siblings

Recruitment status: 
Recruiting

RATIONALE: Gathering health information about patients with neurofibromatosis type 1 over time may help doctors learn more about the disease. PURPOSE: This clinical trial is studying changes over time in patients with neurofibromatosis type 1 and their healthy siblings.

Background information
Trial ID: 
NCT00693394
Other unique IDs: 
CDR0000589012
NCI-08-C-0079
NCI-P07283
Official title: 

Natural History Study and Longitudinal Assessment of Children, Adolescents, and Adults With Neurofibromatosis Type 1

Detailed description: 

OBJECTIVES:

  • To serve as an umbrella protocol for the ongoing neurofibromatosis type 1 (NF1) clinical trials program to longitudinally characterize and analyze NF1-related tumor and non-tumor manifestations and to develop a better understanding of the biology of NF1-related manifestations.
  • To provide the basis for the development of endpoints for clinical trials and to potentially develop more effective treatments.
  • To evaluate whole-body tumor burden in children with plexiform neurofibromas (PN) longitudinally.
  • To analyze growth rate of PN in children and
Number to be enrolled: 
200 patients

Observing Young Patients With Ependymoma Undergoing Standard Combination Chemotherapy

Trial phase: 
Phase III
Recruitment status: 
Recruiting

RATIONALE: Gathering information about how young patients with ependymoma respond to standard combination chemotherapy and learning about the long-term effects of this treatment may help doctors plan better treatment. PURPOSE: This phase III trial is observing young patients with ependymoma undergoing standard combination chemotherapy.

Background information
Trial ID: 
NCT00683319
Other unique IDs: 
CDR0000590666
CCLG-CNS-2007-09
EU-20835
Official title: 

CCLG Observational Study of the Outcome of Ependymoma in Infants Diagnosed Before Their Third Birthday

Detailed description: 

OBJECTIVES: Primary

  • To determine the overall survival and event-free survival of all infants diagnosed with ependymoma before their third birthday.
  • To determine the overall survival and event-free survival of infants diagnosed with ependymoma before their third birthday when treated with standard chemotherapy comprising vincristine, carboplatin, high-dose methotrexate, cyclophosphamide, and cisplatin.

Number to be enrolled: 
50 patients

Cilengitide in Treating Younger Patients With Recurrent or Progressive High-Grade Glioma That Has Not Responded to Standard Therapy

Trial phase: 
Phase II
Recruitment status: 
Suspended

RATIONALE: Cilengitide may stop the growth of tumor cells by blocking blood flow to the tumor. PURPOSE: This phase II trial is studying how well cilengitide works in treating younger patients with recurrent or progressive high-grade glioma that has not responded to standard therapy.

Background information
Trial ID: 
NCT00679354
Other unique IDs: 
CDR0000595623
COG-ACNS0621
Official title: 

Cilengitide (EMD 121974) (IND# 59073) in Recurrent or Progressive and Refractory Childhood High-Grade Glioma

Detailed description: 

OBJECTIVES: Primary

  • To determine the objective response rate to cilengitide in younger patients with recurrent or progressive high-grade glioma that is refractory to standard therapy.

Secondary

  • To estimate the distribution of time to progression, time to treatment failure, and time to death in these patients.
  • To estimate the rate of toxicity, especially symptomatic intratumoral hemorrhage, in these patients.

Number to be enrolled: 
24 patients

Temozolomide, Carmustine, O6-Benzylguanine, Radiation Therapy, and an Autologous Stem Cell Transplant in Treating Patients With Newly Diagnosed Glioblastoma Multiforme or Gliosarcoma

RATIONALE: Giving chemotherapy and radiation therapy before a peripheral stem cell transplant stops the growth of cancer cells by stopping them from dividing or killing them. Giving colony-stimulating factors, such as G-CSF, and certain chemotherapy drugs, helps stem cells move from the bone marrow to the blood so they can be collected and stored. Chemotherapy or radiation therapy is then given to prepare the bone marrow for the stem cell transplant. The stem cells are then returned to the patient to replace the blood-forming cells that were destroyed by the chemotherapy and radiation therapy. PURPOSE: This phase I trial is studying the best dose of temozolomide when given together with radiation therapy, carmustine, O6-benzylguanine, and an autologous stem cell transplant in treating patients with newly diagnosed glioblastoma multiforme or gliosarcoma.

Background information
Other unique IDs: 
CDR0000586180
FHCRC-2000.00
FHCRC-IR-6259

Tandutinib and Bevacizumab in Treating Patients With Recurrent High-Grade Glioma

RATIONALE: Tandutinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving tandutinib together with bevacizumab may kill more tumor cells. PURPOSE: This phase II trial is studying the side effects of giving tandutinib together with bevacizumab and to see how well it works in treating patients with recurrent high-grade glioma.

Background information
Other unique IDs: 
CDR0000594111
NCI-08-C-0101
P07260

Cediranib, Temozolomide, and Radiation Therapy in Treating Patients With Newly Diagnosed Glioblastoma

RATIONALE: Cediranib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving cediranib together with temozolomide and radiation therapy may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of cediranib to see how well it works when given together with temozolomide and radiation therapy in treating patients with newly diagnosed glioblastoma.

Background information
Other unique IDs: 
CDR0000593717
MGH-07-344
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