Bacci Gaetano, Forni Cristiana, Ferrari Stefano, Longhi Alessandra, Bertoni Franco, Mercuri Mario, Donati Davide, Capanna Rodolfo, Bernini Gabriella, Briccoli Antonio, Setola Elisabetta, Versari Michela
Chemotherapy, Department of Musculoskeletal Oncology, Istituto Ortopedico Rizzolo, Bologna, Italy.
J Pediatr Hematol Oncol. 2003 Nov;25(11):845-53. doi: 10.1097/00043426-200311000-00006.
The aim of this study was to compare the results in terms of histologic response to primary chemotherapy of two sequential studies in osteosarcoma patients preoperatively treated with methotrexate, doxorubicin, cisplatin, and ifosfamide, given at different doses.
Between January 1993 and March 1995, 171 patients with osteosarcoma of the extremity were treated according to a protocol of neoadjuvant chemotherapy with preoperative methotrexate, cisplatin, doxorubicin, and ifosfamide. From April 1995 to December 1999, 196 osteosarcoma patients were preoperatively treated with the same drugs at higher doses. Postoperatively, patients received the same treatment in both studies used, but poor responders (tumor necrosis <95%) had more cycles of treatment than good responders.
Comparing the two chemotherapy regimens, there were no significant differences in terms of good histologic response to chemotherapy (69% vs. 62%), 5-year event-free survival (60% vs. 65%), 5-year overall survival (74% vs. 80%), and rate of local recurrence (6% vs. 4%). The 5-year event-free survival was significantly related to the serum level of alkaline phosphatase before treatment (77% for patients with normal values vs. 46% for patients with high values) and the degree of histologic response to preoperative chemotherapy (69% for good responders vs. 54% for poor responders).
Increasing the doses of preoperative chemotherapy does not improve the rate of good histologic response and survival in osteosarcoma of the extremity. The degree of necrosis induced by preoperative treatment probably reflects an innate sensitivity to chemotherapy, which is not altered by increasing drug doses.
本研究旨在比较骨肉瘤患者术前接受不同剂量甲氨蝶呤、阿霉素、顺铂和异环磷酰胺进行原发性化疗后的组织学反应结果。
1993年1月至1995年3月期间,171例肢体骨肉瘤患者按照新辅助化疗方案接受术前甲氨蝶呤、顺铂、阿霉素和异环磷酰胺治疗。1995年4月至1999年12月期间,196例骨肉瘤患者术前接受相同药物的更高剂量治疗。术后,两项研究中的患者均接受相同治疗,但反应不佳者(肿瘤坏死<95%)比反应良好者接受更多周期的治疗。
比较两种化疗方案,化疗后良好组织学反应(69%对62%)、5年无事件生存率(60%对65%)、5年总生存率(74%对80%)和局部复发率(6%对4%)方面无显著差异。5年无事件生存率与治疗前血清碱性磷酸酶水平(正常值患者为77%,高值患者为46%)及术前化疗的组织学反应程度(反应良好者为69%,反应不佳者为54%)显著相关。
增加术前化疗剂量并不能提高肢体骨肉瘤的良好组织学反应率和生存率。术前治疗诱导的坏死程度可能反映了对化疗的固有敏感性,增加药物剂量并不能改变这一点。