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Melatonin and Radiation Therapy in Treating Patients With Brain Metastases
This study has been completed.
Study NCT00031967   Information provided by National Cancer Institute (NCI)
First Received: March 8, 2002   Last Updated: August 29, 2009   History of Changes

March 8, 2002
August 29, 2009
May 2002
 
 
 
Complete list of historical versions of study NCT00031967 on ClinicalTrials.gov Archive Site
 
 
 
Melatonin and Radiation Therapy in Treating Patients With Brain Metastases
A Randomized Phase II Study of A.M. and P.M. Melatonin for Brain Metastasis in RPA Class II Patients

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs such as melatonin may make tumor cells more sensitive to radiation therapy and may protect normal cells from the side effects of radiation therapy.

PURPOSE: Randomized phase II trial to determine the effectiveness of combining melatonin with radiation therapy in treating patients who have brain metastases.

OBJECTIVES:

  • Determine the effect of melatonin, used as radiosensitization/radioprotection, on overall survival and clinical deterioration in patients with brain metastases who are undergoing radiotherapy.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to planned chemotherapy after whole brain irradiation (yes vs no). Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients undergo whole brain irradiation once daily 5 days a week for 2 weeks. Patients receive oral melatonin once daily every morning.
  • Arm II: Patients undergo whole brain irradiation as in arm I. Patients receive oral melatonin once daily every evening.

All patients continue on melatonin for 6 months in the absence of disease progression or unacceptable toxicity.

Patients are followed at months 6 and 12 from start of radiotherapy and then every 6 months thereafter.

PROJECTED ACCRUAL: A total of 128 patients (64 per treatment arm) will be accrued for this study within 5 months.

Phase II
Interventional
Treatment, Randomized, Active Control
  • Metastatic Cancer
  • Radiation Toxicity
  • Unspecified Adult Solid Tumor, Protocol Specific
  • Drug: therapeutic melatonin
  • Radiation: radiation therapy
 
Berk L, Berkey B, Rich T, Hrushesky W, Blask D, Gallagher M, Kudrimoti M, McGarry RC, Suh J, Mehta M. Randomized phase II trial of high-dose melatonin and radiation therapy for rpa class 2 patients with brain metastases (RTOG 0119). Int J Radiat Oncol Biol Phys. 2007 Apr 5; [Epub ahead of print]

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
 
 
 

DISEASE CHARACTERISTICS:

  • Histologically confirmed solid tumor with brain metastasis

    • No germ cell tumors
  • RPA class II with any of the following:

    • At least 65 years of age
    • Extracranial metastases
    • Uncontrolled primary malignancy
  • Ineligible for or unwilling to participate in alternative RTOG stereotactic radiosurgery studies

PATIENT CHARACTERISTICS:

Age:

  • See Disease Characteristics

Performance status:

  • Zubrod 0-1

Life expectancy:

  • Not specified

Hematopoietic:

  • Not specified

Hepatic:

  • Not specified

Renal:

  • Not specified

Other:

  • Able to swallow pills
  • Not pregnant
  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • More than 30 days since prior chemotherapy
  • Concurrent chemotherapy after whole brain irradiation allowed

Endocrine therapy:

  • Not specified

Radiotherapy:

  • See Disease Characteristics
  • No prior radiotherapy to the brain

Surgery:

  • Not specified
Both
 
No
Contact information is only displayed when the study is recruiting subjects
United States,   Canada
 
NCT00031967
 
CDR0000069245, RTOG-BR-0119, RTOG-DEV-1013
Radiation Therapy Oncology Group
National Cancer Institute (NCI)
Study Chair: Lawrence B. Berk, MD, PhD Newark Radiation Oncology
National Cancer Institute (NCI)
March 2004

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP