Chou Alexander J, Kleinerman Eugenie S, Krailo Mark D, Chen Zhengjia, Betcher Donna L, Healey John H, Conrad Ernest U, Nieder Michael L, Weiner Michael A, Wells Robert J, Womer Richard B, Meyers Paul A
Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Cancer. 2009 Nov 15;115(22):5339-48. doi: 10.1002/cncr.24566.
The addition of liposomal muramyl tripeptide phosphatidylethanolamine (MTP-PE) to chemotherapy has been shown to improve overall survival in patients with nonmetastatic osteosarcoma (OS). The authors report the results of addition of liposomal MTP-PE to chemotherapy for patients with metastatic OS.
Intergroup-0133 was a prospective randomized phase 3 trial for the treatment of newly diagnosed patients with OS. The authors compared 3-drug chemotherapy with cisplatin, doxorubicin, and high-dose methotrexate (Regimen A) to the same 3 drugs with the addition of ifosfamide (Regimen B). The addition of liposomal MTP-PE to chemotherapy was evaluated.
Five-year event-free survival (EFS) for patients who received liposomal MTP-PE (n = 46) was 42% versus 26% for those who did not (n = 45) (relative risk for liposomal MTP-PE, 0.72; P = .23; 95% confidence interval [CI], 0.42-1.2). The 5-year overall survival for patients who received MTP-PE versus no MTP-PE was 53% and 40%, respectively (relative risk for liposomal MTP-PE, 0.72; P = 0.27; 95% CI, 0.40-1.3). The comparison of Regimen A with Regimen B did not suggest a difference for EFS (35% vs 34%, respectively; relative risk for Regimen B, 1.07; P = .79; 95% CI, 0.62-1.8) or overall survival (52% vs 43%, respectively; relative risk for Regimen B, 1.1, P = .75; 95% CI, 0.61-2.0).
When the metastatic cohort was considered in isolation, the addition of liposomal MTP-PE to chemotherapy did not achieve a statistically significant improvement in outcome. However, the pattern of outcome is similar to the pattern in nonmetastatic patients.
已证明在化疗中添加脂质体胞壁酰三肽磷脂酰乙醇胺(MTP-PE)可提高非转移性骨肉瘤(OS)患者的总生存率。作者报告了在转移性OS患者的化疗中添加脂质体MTP-PE的结果。
0133组间研究是一项用于治疗新诊断OS患者的前瞻性随机3期试验。作者将顺铂、阿霉素和大剂量甲氨蝶呤的三联化疗(方案A)与添加异环磷酰胺的相同三种药物(方案B)进行了比较。评估了在化疗中添加脂质体MTP-PE的效果。
接受脂质体MTP-PE的患者(n = 46)的5年无事件生存率(EFS)为42%,而未接受脂质体MTP-PE的患者(n = 45)为26%(脂质体MTP-PE的相对风险,0.72;P = 0.23;95%置信区间[CI],0.42 - 1.2)。接受MTP-PE与未接受MTP-PE的患者的5年总生存率分别为53%和40%(脂质体MTP-PE的相对风险,0.72;P = 0.27;95%CI,0.40 - 1.3)。方案A与方案B的比较未显示EFS有差异(分别为35%和34%;方案B的相对风险,1.07;P = 0.79;95%CI,0.62 - 1.8)或总生存率有差异(分别为52%和43%;方案B的相对风险,1.1,P = 0.75;95%CI,0.61 - 2.0)。
单独考虑转移性队列时,在化疗中添加脂质体MTP-PE并未在结局上取得统计学显著改善。然而,结局模式与非转移性患者的模式相似。