Accelerated hyperfractionated radiotherapy for malignant gliomas

Int J Radiat Oncol Biol Phys. 1996 Mar 1;34(4):785-92. doi: 10.1016/0360-3016(95)02157-4.

Abstract

Purpose: To evaluate accelerated hyperfractionated radiotherapy for the treatment of malignant gliomas.

Methods and materials: Between April 1985 and June 1994, 70 adult patients with pathologically confirmed malignant glioma (75% glioblastoma multiforme, 25% anaplastic astrocytoma) suitable for high-dose therapy were selected for treatment with accelerated hyperfractionated radiotherapy, 1.5 Gy twice daily to a total target dose of 60 Gy. Two patients were excluded from analysis (one patient had a fatal pulmonary embolism after 18 Gy; one patient discontinued therapy after 28.5 Gy against medical advice and without sequelae or progression). The 68 patients in the study group had a median age of 52 years and a median Karnofsky performance status of 90. Stereotactic implant (125I) or stereotactic radiosurgery boosts were delivered to 16 patients (24%) in the study group. Minimum follow-up was 6 months.

Results: Median survival was 13.8 months and median progression-free survival was 7.4 months. The absolute Kaplan-Meier survival rate was 16% at 2 years and 4% at 5 years. Multivariate analysis for the prognostic impact of age, gender, histology, Karnofsky performance status, symptomatology, surgical resection vs. biopsy, and boost vs. nonboost therapy revealed that Karnofsky performance status > or = 90, boost therapy, and surgical excision predicted significantly improved outcome. No severe toxicity occurred in patients treated with accelerated hyperfractionated radiotherapy alone, although 5% required steroids temporarily for edema. Progression occurred during treatment in one patient (1.5%).

Conclusion: This regimen of accelerated hyperfractionated radiotherapy is well tolerated and leads to results comparable with those of standard therapy. The rate of disease progression during treatment is significantly better (p = 0.001) than is reported for patients treated with standard fractionation, with or without chemotherapy. This regimen is a reasonable starting point for future trials and may have some advantages over standard fractionation.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Analysis of Variance
  • Brain Edema / etiology
  • Brain Neoplasms / radiotherapy*
  • Brain Neoplasms / surgery
  • Combined Modality Therapy
  • Disease-Free Survival
  • Female
  • Glioblastoma / radiotherapy*
  • Glioblastoma / surgery
  • Humans
  • Male
  • Middle Aged
  • Radiosurgery
  • Radiotherapy / adverse effects
  • Radiotherapy Dosage
  • Reoperation