Status:

COMPLETED

Study of Blood Samples and Risk of Infection in Patients With Newly Diagnosed Malignant Supratentorial Astrocytoma

Lead Sponsor:

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Collaborating Sponsors:

National Cancer Institute (NCI)

North American Brain Tumor Consortium

Conditions:

Brain and Central Nervous System Tumors

Infection

Eligibility:

All Genders

18+ years

Brief Summary

RATIONALE: Gathering information over time from laboratory tests of patients with newly diagnosed malignant supratentorial astrocytoma may help doctors learn more about the effect of treatment on whit...

Detailed Description

OBJECTIVES: * Determine the frequency and severity of decreases in CD4 counts as a function of therapy in patients with newly diagnosed malignant astrocytoma. * Determine whether the decrease in CD4 ...

Eligibility Criteria

Inclusion

  • DISEASE CHARACTERISTICS:
  • Histologically confirmed primary malignant brain tumor in 1 of the following groups:
  • High grade (grade III or IV) supratentorial glioma receiving antineoplastic treatment and with 1 of the following histologies:
  • Anaplastic astrocytoma
  • Glioblastoma multiforme (giant cell glioblastoma or gliosarcoma)
  • Anaplastic oligodendroma
  • Low grade (grade I or II) supratentorial glioma not planning to receive treatment of any kind (including steroids) and with 1 of the following histologies:
  • Astrocytoma
  • Oligodendroglioma
  • PATIENT CHARACTERISTICS:
  • Karnofsky performance status 60-100%
  • No HIV positivity
  • PRIOR CONCURRENT THERAPY:
  • No prior chemotherapy for brain tumor except polifeprosan 20 with carmustine implant (Gliadel® wafer)
  • No prior cranial radiotherapy or radiotherapy for brain tumor
  • No prior immunotherapy or biologic agents for brain tumor, including any of the following:
  • Immunotoxins
  • Immunoconjugates
  • Peptide receptor antagonists
  • Interleukins
  • Interferons
  • Tumor-infiltrating lymphocytes
  • Lymphokine-activated killer cell therapy
  • Gene therapy
  • Antisense therapy
  • No prior hormonal therapy for brain tumor
  • More than 14 days since prior and no concurrent steroid therapy for patients with low-grade (grade I or II) astrocytoma
  • Prior glucocorticoid therapy allowed

Exclusion

    Key Trial Info

    Start Date :

    July 1 2004

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    Estimated Enrollment :

    104 Patients enrolled

    Trial Details

    Trial ID

    NCT00999622

    Start Date

    July 1 2004

    Last Update

    May 28 2012

    Active Locations (0)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 0 (0 locations)

    No Results Found

    We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.