Goorin Allen M, Schwartzentruber Douglas J, Devidas Meenakshi, Gebhardt Mark C, Ayala Alberto G, Harris Michael B, Helman Lee J, Grier Holcombe E, Link Michael P
Dana-Farber Cancer Institute, 44 Binney St, Boston, MA 02115, USA.
J Clin Oncol. 2003 Apr 15;21(8):1574-80. doi: 10.1200/JCO.2003.08.165.
Successful therapeutic interventions to prevent disease progression in patients with nonmetastatic osteosarcoma have included surgery with adjuvant chemotherapy. Presurgical chemotherapy has been advocated for these patients because of putative improvement in event-free survival (EFS). The advantages of presurgical chemotherapy include early administration of systemic chemotherapy, shrinkage of primary tumor, and pathologic identification of risk groups. The theoretic disadvantage is that it exposes a large tumor burden to marginally effective chemotherapy. The contribution of chemotherapy and surgery timing has not been tested rigorously.
Between 1986 and 1993, we conducted a prospective trial in patients with nonmetastatic osteosarcoma who were assigned randomly to immediate surgery or presurgical chemotherapy. Except for the timing of surgery (week 0 or 10), patients received 44 weeks of identical combination chemotherapy that included high-dose methotrexate with leucovorin rescue, doxorubicin, cisplatin, bleomycin, cyclophosphamide, and dactinomycin.
One hundred six patients were enrolled onto this study. Six were excluded from analysis. Of the remaining 100 patients, 45 were randomly assigned to immediate chemotherapy, and 55 were randomly assigned to immediate surgery. Sixty-seven patients remain disease-free. At 5 years, the projected EFS +/- SE is 65% +/- 6% (69% +/- 8% for immediate surgery and 61% +/- 8% for presurgical chemotherapy; P =.8). The treatment arms had similar incidence of limb salvage (55% for immediate surgery and 50% for presurgical chemotherapy).
Chemotherapy was effective in both treatment groups. There was no advantage in EFS for patients given presurgical chemotherapy.
成功的治疗干预措施可预防非转移性骨肉瘤患者的疾病进展,其中包括手术联合辅助化疗。由于无事件生存期(EFS)可能得到改善,因此提倡对这些患者进行术前化疗。术前化疗的优点包括早期给予全身化疗、缩小原发肿瘤以及对风险组进行病理识别。理论上的缺点是它使大量肿瘤负荷暴露于疗效欠佳的化疗中。化疗和手术时机的作用尚未得到严格检验。
1986年至1993年间,我们对非转移性骨肉瘤患者进行了一项前瞻性试验,将患者随机分配至立即手术组或术前化疗组。除手术时间(第0周或第10周)外,患者接受44周相同的联合化疗,包括大剂量甲氨蝶呤加亚叶酸解救、阿霉素、顺铂、博来霉素、环磷酰胺和放线菌素D。
106例患者纳入本研究。6例被排除在分析之外。其余100例患者中,45例随机分配至立即化疗组,55例随机分配至立即手术组。67例患者仍无疾病。5年时,预计的EFS±SE为65%±6%(立即手术组为69%±8%,术前化疗组为61%±8%;P = 0.8)。治疗组的保肢发生率相似(立即手术组为55%,术前化疗组为50%)。
两个治疗组的化疗均有效。术前化疗患者在EFS方面无优势。