Purpose: To investigate feasibility, toxicity and antitumor activity of com
bined surgery, postoperative radiation therapy (RT) and adjuvant chemothera
py (CHT) in adult patients with pure anaplastic oligodendroglioma (PAO) or
mixed anaplastic oligoastrocytoma (MAO).
Methods: Between January 1988, and June 1993, 23 patients entered into a ph
ase II study. After surgery, post-operative RT was administered with 60 Gy
in 30 daily fractions in 30 treatment days in 6 weeks. Two weeks after RT,
adjuvant 'modified' PCV (mPCV) (Procarbazine, 60 mg/m(2), days 1-14; CCNU,
100 mg/m(2), day 1; and vincristine, 1.4 mg/m(2) (max. 2 mg), days 1 and 8)
was administered every six weeks up to six cycles or until progression occ
urred.
Results: Median survival time is not attained yet, while 1-5 year survival
rates are 100%, 100%, 78%, 61%, and 52%, respectively. Median time to tumor
progression is not attained yet, while 1-5 year progression-free survival
rates are 100%, 100%, 70%, 52%, and 52%, respectively. On univariate analys
is of potential prognostic factors, sex, tumor location (frontal versus oth
er), and histology (pure versus mixed anaplastic oligodendroglioma) were no
t found to influence survival. Age of < 50 years carried improved prognosis
as well as Karnofsky performance status (KPS) 90-100 when compared to KPS
of 70-80. Patients having tumors less than or equal to 4 cm did better than
those with tumors > 4 cm as well as those with total tumor resection when
compared to those with subtotal tumor resection or biopsy only. Acute high-
grade (greater than or equal to 3) CHT-related toxicity was mainly hematolo
gical with only 3 (13%) patients experiencing acute grade 4 toxicity.
Conclusions: Combined treatment modality consisting of surgery, postoperati
ve high-dose RT and mPCV chemotherapy for patients with anaplastic oligoden
droglioma was effective with acceptable toxicity. Further studies are neede
d with more patients and longer follow-up to verify these results in this r
are disease.