B. Jeremic et al., ACCELERATED HYPERFRACTIONATED RADIATION-THERAPY FOR MALIGNANT GLIOMA - A PHASE-II STUDY, American journal of clinical oncology, 18(5), 1995, pp. 449-453
Sixty-four adult patients with malignant glioma entered into a Phase I
I study on the use of accelerated hyperfractionated radiation therapy,
Histology included anaplastic astrocytoma (AA) in 15 patients and gli
oblastoma multiforme (GEM) in 49 patients. Treatment consisted of radi
ation therapy doses of 66 Gy in 44 fractions in 22 treatment days in 4
.5 weeks, fractions of 1.5 Gy, b.i.d. 1,3-bis(2-chlorethyl)-1-nitrosou
rea (BCNU) 80 mg/m(2) and hydroxyurea 800 mg/m(2) were both given on t
reatment days 1, 6, 11, 16, and 21 during the irradiation course. Medi
an survival time for all 64 patients is 61 weeks (range: 12-163 weeks)
from the date of starting irradiation, Median time to tumor progressi
on (MTP) for GEM patients is 31 weeks, and 1-year and 3-year progressi
on-free survival (PFS) are 16% and 0%, respectively, while MTP for AA
patients is not attained yet, and 1-year and 3-year PFS are 100% and 7
3%, respectively. On univariate analysis of prognostic factors for GEM
patients, younger age, total or subtotal tumor removal, and frontal t
umor location are associated with a better prognosis. A multivariate a
nalysis confirmed the importance of the extent of surgery and tumor si
te and revealed the interfraction interval (4.5-5.0 hours vs 5.5-6.0 h
ours, p =.041) as an important prognostic factor. Acute and late toxic
ity is not increased. Longer follow-up and more patients are needed to
evaluate tumor control and toxicity in AA patients.