Between 1975 and 1990, eighteen patients with a histologically proven
diagnosis of chordoma were treated at our institution. All patients in
itially underwent a surgical procedure and were referred for irradiati
on due to residual disease or postsurgical relapse. The mean dose admi
nistered was 50.1 Gy (range, 29.9-64.8 Gy). Eight patients were treate
d according to a hyperfractionated schedule. The overall actuarial 5-y
ear survival and 5-year progression-free survival were 38% and 17%, re
spectively. The progression-free interval was longer for patients rece
iving doses greater than 48 Gy when compared with doses below 40 Gy (a
ctuarial 5-year progression-free survival of 31 +/- 35% vs. 0%, respec
tively; p = 0.04). We conclude that in the treatment of chordoma. the
administration of high radiation doses may increase the disease-free i
nterval. The objective response and dose-response relationships were a
nalyzed in twelve patients for whom sequential CT scans were available
.