Prevention of chemotherapy-induced febrile neutropenia by prophylactic antibiotics plus or minus granulocyte colony-stimulating factor in small-cell lung cancer: A Dutch randomized phase III study

被引:141
作者
Timmer-Bonte, JN
de Boo, TM
Smit, HJ
Biesma, B
Wilschut, FA
Cheragwandi, SA
Termeer, A
Hensing, CA
Akkermans, J
Adang, EM
Bootsma, GP
Tjan-Heijnen, VC
机构
[1] Radboud Univ Nijmegen, Rijnstate Hosp, Ctr Med, Dept Med Oncol, Arnhem, Netherlands
[2] Radboud Univ Nijmegen, Rijnstate Hosp, Ctr Med, Dept Epidemiol & Biostat, Arnhem, Netherlands
[3] Radboud Univ Nijmegen, Rijnstate Hosp, Ctr Med, Dept Pulmonol, Arnhem, Netherlands
[4] Radboud Univ Nijmegen, Rijnstate Hosp, Ctr Med, Dept Med Technol Assesment, Arnhem, Netherlands
[5] Jeroen Bosch Hosp, GZG Hertogenbosch, Nijmegen, Netherlands
[6] Hosp Gelderse Vallei Ede, Nijmegen, Netherlands
[7] Hosp Koningen Beatrix Winterswijk, Nijmegen, Netherlands
[8] Canisius Wilhelmina Hosp Nijmegen, Nijmegen, Netherlands
[9] Diaconessenhuis Meppel, Nijmegen, Netherlands
[10] Ctr Comprehens Canc, Trial Off, Nijmegen, Netherlands
关键词
D O I
10.1200/JCO.2004.00.7955
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Febrile neutropenia (FN) is a major complication of chemotherapy. Antibiotics as well as granulocyte colony-stimulating factor (G-CSF) are effective in preventing FIN. This multicenter randomized phase III trial determines whether the addition of G-CSF to antibiotic prophylaxis can further reduce the incidence of FIN in patients with small-cell lung cancer (SCLC) at the risk of FN. Patients and Methods Patients (N = 175) were stratified for stage of disease, performance status, age, and prior chemotherapy treatment, and were randomly assigned for treatment with cyclophosphamide, doxorubicin, and etoposide (CDE), followed by prophylactic antibiotics alone (ciprofloxacin and roxithromycin) or by antibiotics in combination with G-CSF on days 4 to 13. Results In cycle 1, 20 patients (24%) in the antibiotics group developed FN compared with nine patients (10%) in the antibiotics plus G-CSF group (P = .01). In cycles 2 to 5, the incidences of FN were practically the same in both groups (17% v 11%). Only the treatment parameters (odds ratio, 0.33; 95% CI, 0.14 to 0.78) and age (1.067 per year; 95% CI, 1.013 to 1.0124) were related to the probability of FN in cycle 1. Conclusion Primary G-CSF prophylaxis added to primary antibiotic prophylaxis is effective in reducing FIN and infections in SCLC patients at the risk of FN with the first cycle of CDE chemotherapy. For patients with similar risk of FIN, the combined use of prophylactic antibiotics plus G-CSF can be considered, specifically in the first cycle of chemotherapy.
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页码:7974 / 7984
页数:11
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