Long-term results after combined modality treatment for non-metastatic osteosarcoma

被引:14
作者
Aparicio, J [1 ]
Segura, A [1 ]
Montalar, J [1 ]
Garcerá, S [1 ]
Oltra, A [1 ]
Santaballa, A [1 ]
Yuste, A [1 ]
Pastor, M [1 ]
Munárriz, B [1 ]
机构
[1] Hosp Univ La Fe, Dept Med Oncol, Med Oncol Serv, E-46009 Valencia, Spain
关键词
localised osteosarcoma; multimodal therapy; long-term survival; prognostic factors;
D O I
10.1007/BF02785871
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Since the introduction of multimodality treatment, the prognosis of patients 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 potential 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-doxorubicin/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-dose 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 survival rates were 64% and 49% at 5 y, and 59% and 49% at 10 y, respectively. Tumour size and primary site were significant prognostic factors for survival in univariate analyses. In conclusion, long-term survival after combined modality treatment can be achieved in more than 60% of patients with localised osteosarcoma, including non-appendicular lesions. Limb-sparing surgery is a realistic goal for most cases. The prognostic value of tumour necrosis and the efficacy of neoadjuvant chemotherapy should be interpreted according to individual high-dose methotrexate scheduling.
引用
收藏
页码:255 / 260
页数:6
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