Since the introduction of multimodality treatment, the prognosis of patient
s with high-grade non-metastatic osteosarcoma has significantly improved. A
retrospective review was performed to assess the long-term results of this
approach in a single centre setting, and to investigate the impact of pote
ntial clinical prognostic factors. Between 1985 and 1993, 35 patients with
stage II-A and II-B osteosarcoma underwent preoperative chemotherapy (high-
dose methotrexate), wide surgery, and adjuvant chemotherapy (cisplatin-doxo
rubicin/bleomycin-cyclophosphamide-dactinomycin) (modified T-10A protocol).
There were 19 males and 16 females. Median patient age was 17 y (range 12-
42). Primary tumour sites were the extremities (83%) and axial bones (17%).
In spite of an unfavourable grade 3-4 histologic response rate to high-dos
e methotrexate of 12%, 31 (88%) patients were able to undergo limb-sparing
surgery and 28 (80%) were rendered disease free after the planned therapy.
Median follow-up was 8 y. The actuarial overall survival and disease-free s
urvival rates were 64% and 49% at 5 y, and 59% and 49% at 10 y, respectivel
y. Tumour size and primary site were significant prognostic factors for sur
vival in univariate analyses. In conclusion, long-term survival after combi
ned modality treatment can be achieved in more than 60% of patients with lo
calised osteosarcoma, including non-appendicular lesions. Limb-sparing surg
ery is a realistic goal for most cases. The prognostic value of tumour necr
osis and the efficacy of neoadjuvant chemotherapy should be interpreted acc
ording to individual high-dose methotrexate scheduling.