Volume 60, Issue 3 , Pages 853-860, 1 November 2004
Randomized comparison of stereotactic radiosurgery followed by conventional radiotherapy with carmustine to conventional radiotherapy with carmustine for patients with glioblastoma multiforme: Report of Radiation Therapy Oncology Group 93-05 protocol☆
Abstract
Purpose
Conventional treatment of glioblastoma multiforme (GBM) cures less than 5% of patients. We investigated the effect of stereotactic radiosurgery (SRS) added to conventional external beam radiation therapy (EBRT) with carmustine (BCNU) on the survival of patients with GBM.
Methods and materials
A total of 203 patients with supratentorial GBM (tumor ≤40 mm) were randomly assigned either to postoperative SRS followed by EBRT (60 Gy) plus BCNU (80 mg/m2 Days 1–3 every 8 weeks for six cycles) or to EBRT with BCNU alone. The dose of radiosurgery was tumor size–dependent and ranged from 15 Gy for largest to 24 Gy for smallest tumors. RT and BCNU were identical in both arms.
Results
At a median follow-up time of 61 months, the median survival in the radiosurgery group was 13.5 months (95% confidence interval, 11.0–14.8) as compared with 13.6 months (95% confidence interval, 11.2–15.2, p = 0.5711) for the standard treatment group. There were also no significant differences in 2- and 3-year survival rates and in patterns of failure between the two arms. Quality of life deterioration and cognitive decline at the end of therapy, compared with baseline, were comparable and there was no difference in quality-adjusted survival between the arms.
Conclusions
Stereotactic radiosurgery followed by EBRT and BCNU does not improve the outcome in patients with GBM nor does it change the general quality of life or cognitive functioning.
Keywords: Stereotactic radiosurgery, Radiation therapy, Glioblastoma multiforme, Quality of life
To access this article, please choose from the options below
☆ Supported by RTOG U10 CA21661, CCOP U10 CA37422, and Stat U10 CA32115 grants from the National Cancer Institute. Its contents are solely the responsibility of the authors and not necessarily represent the official views of the National Cancer Institute.
PII: S0360-3016(04)00645-5
doi:10.1016/j.ijrobp.2004.04.011
© 2004 Elsevier Inc. All rights reserved.
Volume 60, Issue 3 , Pages 853-860, 1 November 2004
