MedPath

Radiosurgery for Glioblastoma Multiforme

Phase 1
Terminated
Conditions
Glioblastoma Multiforme
Interventions
Procedure: CyberKnife
Registration Number
NCT00456612
Lead Sponsor
Beth Israel Deaconess Medical Center
Brief Summary

Conventional radiation for 6 weeks is not well tolerated by the elderly. Shorter courses (over 3-5 weeks) of radiation have been shown to be equivalent in outcome the elderly- particularly in patients who are generally in poor performance status (KPS\<70). Fractionated Cyberknife Radiosurgery can deliver equivalent doses in 5 treatments providing the same tumor control in a much shorter and tolerable schedule improving their quality of their short life.

To assess the tolerability of Cyberknife Radiosurgery for High Grade Gliomas in Elderly with poor performance status.

Secondary:

Assessment of local control rate, progression free survival, overall survival, quality of life and toxicity and steroid dependence in this population with this regime.

Detailed Description

Conventional radiation for 6 weeks is not well tolerated by the elderly. Shorter courses (over 3-5 weeks) of radiation have been shown to be equivalent in outcome the elderly- particularly in patients who are generally in poor performance status (KPS\<70). Fractionated Cyberknife Radiosurgery can deliver equivalent doses in 5 treatments providing the same tumor control in a much shorter and tolerable schedule improving their quality of their short life.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
4
Inclusion Criteria
  1. Histopathologically confirmed newly diagnosed glioblastoma multiforme or Anaplastic Glioma (WHO Grade III) by surgical excision or biopsy.

  2. Patient must recover from the effects of surgery, post-operative infection, or other complications.

  3. Therapy should start within 5 weeks of surgery

  4. Must have an estimated survival of > 8 weeks.

  5. KPS < 70.

  6. Age > 65 years.

  7. Must have a pre- and post operative contrast enhanced MRI scans

  8. Laboratory values within the following limits: ANC (absolute neutrophil count) >/= 1500 cell/ul Platelets >/= 100x 10(3)/ul, Hemoglobin >/= 9g/dl, Serum Creatinine ≤ 1.5mg/dl., Serum total Bilirubin </= 1.5 x upper limit of normal (ULN), SGOT/SGPT </= 2.5x ULN, Albumin >/= 3g/dl.

Exclusion Criteria
  1. Histology grade less than Anaplastic Glioma ( WHO Grade III).

  2. Recurrent malignant glioma.

  3. Tumor involving the Brain stem.

  4. Any detected tumor foci beyond the cranial vault.

  5. Major medical or psychiatric illness, which in the investigator's opinion will prevent administration or completion of the protocol therapy.

  6. Prior malignancies, except for non-melanomatous skin cancers, or carcinoma in situ of uterus, cervix or bladder, unless disease free for > 5 years.

  7. Prior chemotherapy for the current disease.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
CyberknifeCyberKnifeRadiosurgery to enhancing high grade glioma in 5 fractions with escalating doses.
Primary Outcome Measures
NameTimeMethod
The Percent Progression -Free Survival at 6 Months Will be Tabulated6 months
Progression Free Survivalconsent to prgression or death
Secondary Outcome Measures
NameTimeMethod
Response, Median Time to Tumor Progression,Overall Survival, Percent Overall Survival at 1 Year Will be Tabulated.1year

Trial Locations

Locations (1)

Beth Israel Deaconess Medical Center

🇺🇸

Boston, Massachusetts, United States

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