Randomized Trial of Cefozopran Versus Cefepime as Empirical Antibiotic Treatment of Febrile Neutropenia in Pediatric Cancer Patients

被引:16
|
作者
Sarashina, Takeo [1 ]
Kobayashi, Ryoji [2 ]
Yoshida, Makoto [1 ]
Toriumi, Naohisa [1 ]
Suzuki, Daisuke [2 ]
Sano, Hirozumi [2 ]
Azuma, Hiroshi [1 ]
机构
[1] Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, Japan
[2] Sapporo Hokuyu Hosp, Dept Pediat, Sapporo, Hokkaido, Japan
关键词
cefepime; cefozopran; empirical therapy; febrile neutropenia; ANTIMICROBIAL AGENTS; PLUS AMIKACIN; SOLID TUMORS; MONOTHERAPY; THERAPY; METAANALYSIS; CHILDREN; FEVER; PIPERACILLIN/TAZOBACTAM; CEFTAZIDIME;
D O I
10.1002/pbc.25148
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundFebrile neutropenia (FN) is a common and serious complication of cancer chemotherapy associated with significant morbidity and mortality. Cefozopran (CZOP) is a potential candidate for empirical monotherapy in FN. However, studies on the use of CZOP as empirical treatment for pediatric patients with FN are quite limited. The purpose of this study was to compare the efficacy and safety of CZOP with cefepime (CFPM) empirical monotherapy in pediatric cancer patients with FN. ProceduresA total of 64 patients with 224 episodes of FN were randomly assigned to receive antibiotic therapy with either CZOP (100mg/kg/day) or CFPM (100mg/kg/day). Of these episodes, 223 were considered eligible for the study. Success was defined as resolution of febrile episodes and clinical signs of infection within 120hr following the start of antibiotic therapy. ResultsThe success rate was not significantly different between the CZOP (64.0%) and CFPM (56.3%) groups (P=0.275). Duration of fever, duration of antibiotic therapy, and the success rate in patients with blood stream infection did not differ between the two groups. There was no infection-related mortality in the study period. ConclusionBoth CZOP and CFPM as monotherapy appear to be effective and safe in pediatric patients. This study suggests that CZOP has satisfactory efficacy and is well tolerated as initial empirical therapy for pediatric cancer patients with FN. Pediatr Blood Cancer 2014;61:1992-1995. (c) 2014 Wiley Periodicals, Inc.
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收藏
页码:1992 / 1995
页数:4
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