A randomized prospective multicentre trial of cefpirome versus piperacillin-tazobactam in febrile neutropenia

被引:13
作者
Bauduer, F [1 ]
Cousin, T [1 ]
Boulat, O [1 ]
Rigal-Huguet, F [1 ]
Molina, L [1 ]
Fegueux, N [1 ]
Jourdan, E [1 ]
Boiron, JM [1 ]
Reiffers, J [1 ]
机构
[1] CHI Cote Basque, Serv Malad Sang, Dept Hematol, F-64100 Bayonne, France
关键词
neutropenic fever; cefpirome; piperacillin-tazobactam; randomized trial;
D O I
10.3109/10428190109064594
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Fever is frequently the only clinical sign of infection in patients with chemo-induced neutropenia. In this setting, empirical administration of broad spectrum antibiotics must be rapid. The aim of this work was to compare, for the first time, cefpirome (CPO) and piperacillin-tazobactam (PT) in a large randomized trial. Two hundred-eight febrile neutropenic episodes (FNE) (greater than or equal to 38,5 degreesC and ANC less than or equal to 0.5 giga/l) were treated by randomization, as first line therapy, using either CPO 2 g x 2/day (105 cases) or PT 4 g x 3/day (103 cases), alone (CPO:15/PT: 15), or plus aminoglycoside (165 cases, CPO: 82/PT: 83) or quinolone CPO: 2/PT: 2). There were 131 men and 77 women aged between 17 and 83 years (median: 49) who received chemotherapy (n=160) or allogeneic (n=10) or autologous (n=38) stem cell transplantations. Underlying diseases were: acute leukemia (n=131), lymphoma (n=33), myeloma (n=16), solid tumor (n=8), myeloproliferative disorder (n=9), chronic lymphoid leukemia (n=5), aplastic anemia (n=3), myelodysplasia (n=3). Distribution of age, neutropenia duration (median: 17 days), underlying disease, and protocol therapy duration (median: 11 days) was comparable in both arms. A microbiologically documented infection (MDI) was evidenced in 57 cases (27%). Bacteria were isolated from blood cultures in 54 cases (Gram positive: 32 cases). Their in vitro susceptibility rates to CPO and PT were not different. Two days after antibiotics initiation, clinical (fever disappearance) and microbiological (culture negativation) success rates (SR) were 62% for CPO versus 61% for PT and 50% versus 55% respectively in case of MDI (p = 0.89). Two deaths and 77 failures were registered. At the end of protocol, SR (no antibiotic change/absence of superinfection) was 59% with CPO versus 50% with FI(p = 0.27) and 53% versus 40% respectively in the 151 cases with neutropenia greater than or equal to 10 days (p = 0.17). The occurrence of side effects was similar in both arms. In our hands, the efficacy of CPO and PT was comparable for treating FNE.
引用
收藏
页码:379 / 386
页数:8
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