Addition of either lonidamine or granulocyte colony-stimulating factor does not improve survival in early breast cancer patients treated with high-dose epirubicin and cyclophosphamide

被引:68
作者
Papaldo, P
Lopez, M
Cortesi, E
Cammilluzzi, E
Antimi, M
Terzoli, E
Lepidini, G
Vici, P
Barone, C
Ferretti, G
Di Cosimo, S
Nistic, C
Carlini, P
Conti, F
Di Laura, L
Botti, C
Vitucci, C
Fabi, A
Giannarelli, D
Marolla, P
机构
[1] Regina Elena Inst Canc Res, Dept Surg, Rome, Italy
[2] Regina Elena Inst Canc Res, Div Med Oncol A, Dept Med Oncol, I-00144 Rome, Italy
[3] Univ Roma La Sapienza, Div Med Oncol, Sch Med, Rome, Italy
[4] S Filippo Neri Hosp, Div Med Oncol, Rome, Italy
[5] S Eugenio Hosp, Div Med Oncol, Rome, Italy
[6] San Camillo Hosp, Div Med Oncol, Rome, Italy
[7] Univ Sacred Heart, Sch Med, Div Med Oncol, I-00168 Rome, Italy
关键词
D O I
10.1200/JCO.2003.03.034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose : Lonidamine (LND) can enhance the activity of anthracyclines in patients with metastatic breast cancer. A multicenter, prospective, randomized trial was designed to determine whether the association of LND with high-dose epirubicin plus cyclophosphamide (EC) could improve disease-free survival (DFS) in patients with early breast cancer (BC) compared with EC alone. Granulocyte colony-stimulating factor (G-CSF) was added to maintain the EC dose-intensity. Patients and Methods: From October 1991 to April 1994, 506 patients with stage I/II BC Were randomly assigned to four groups: (A) epirubicin 120 mg/m(2) and cyclophosphamide 600 mg/m(2) administered intravenously on day 1 every 21 days for four cycles (124 patients); (B) EC plus LND 450 mg/d administered orally (125 patients); (C) EC plus G-CSF administered subcutaneously (129 patients); (D) EC plus LND plus G-CSF (128 patients). Results: Median follow-up was 55 months. Five-year DFS rate was similar for LND (B+D groups; 69.6%) versus non-LND arms (A+C groups; 70.3%) and G-CSF (C+D groups; 67.2%) versus non-G-CSF arms (A+B groups; 72.9%). Five-year overall survival (OS) was comparable in LND (79.1%) versus nonAND arms (81.3%) and in G-CSF (80.6%) versus non-G-CSF arms (79.6%). DFS and OS distributions in LND and G-CSF arms did not change according to tumor size, node, receptor, and menopausal status. G-CSF dramatically reduced hematologic toxicity without having a significant impact on dose-intensity (98.1% v 95.5% for C+D and A+B groups, respectively). Conclusion: EC is active and well tolerated in patients with. early breast cancer. The addition of LND or G-CSF does not improve DFS or OS. (C) 2003 by American Society of Clinical Oncology.
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页码:3462 / 3468
页数:7
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