Addition of Muramyl Tripeptide to Chemotherapy for Patients With Newly Diagnosed Metastatic Osteosarcoma

被引:234
作者
Chou, Alexander J. [1 ]
Kleinerman, Eugenie S. [2 ]
Krailo, Mark D. [3 ]
Chen, Zhengjia [4 ]
Betcher, Donna L. [5 ]
Healey, John H. [6 ]
Conrad, Ernest U., III [7 ]
Nieder, Michael L. [8 ]
Weiner, Michael A. [9 ]
Wells, Robert J. [10 ]
Womer, Richard B. [11 ]
Meyers, Paul A. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10065 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USA
[3] Univ So Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA 90033 USA
[4] Childrens Oncol Grp, Arcadia, CA USA
[5] Mayo Clin, Sect Pediat Hematol Oncol, Rochester, MN USA
[6] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10065 USA
[7] Univ Washington, Dept Orthopaed & Sports Med, Seattle, WA 98195 USA
[8] Univ S Florida, All Childrens Hosp, St Petersburg, FL 33701 USA
[9] Columbia Presbyterian Coll Phys & Surg, Div Pediat Oncol, New York, NY USA
[10] Univ Texas MD Anderson Canc Ctr, Dept Pediat Hematol Oncol, Houston, TX 77030 USA
[11] Childrens Hosp Philadelphia, Div Oncol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
muramyl tripeptide; metastatic osteosarcoma; survival; Children's Oncology Group; PROGNOSTIC-FACTORS; NEOADJUVANT CHEMOTHERAPY; OSTEOGENIC-SARCOMA; CGP; 19835A; THERAPY; IFOSFAMIDE; METHOTREXATE; DOXORUBICIN; EXPERIENCE; CISPLATIN;
D O I
10.1002/cncr.24566
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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. METHODS: 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. RESULTS: 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). CONCLUSIONS: 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. Cancer 2009;115:5339-48. (C) 2009 American Cancer Society.
引用
收藏
页码:5339 / 5348
页数:10
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