Once-per-cycle pegfilgrastim versus daily filgrastim in pediatric patients with Ewing sarcoma

被引:30
作者
Wendelin, G [1 ]
Lackner, H [1 ]
Schwinger, W [1 ]
Sovinz, P [1 ]
Urban, C [1 ]
机构
[1] Med Univ Graz, Div Pediat Hematol & Oncol, Dept Pediat & Adolescent Med, A-8036 Graz, Austria
关键词
pegfilgrastim; neutropenia; pediatric; children;
D O I
10.1097/01.mph.0000175711.73039.63
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The use of the recombinant human granulocyte colony-stimulating factor filgrastim to shorten the duration of severe neutropenia after cytotoxic chemotherapy has become an integral part of supportive care. However, due to its short serum half-life, filgrastim must be injected daily. Pegfilgrastim, a new long-lasting form of filgrastim administrated once per cycle, has been shown in adults to be as effective in reducing the duration of severe neutropenia as daily filgrastim. The aim of this study was to evaluate the effects of pegfilgrastim in pediatric patients. Five children with Ewing sarcoma were alternately treated with a single 100 mu g/kg pegfilgrastim dose or daily doses of 10 mu g/kg Filgrastim after a total number of 58 chemotherapy cycles. Pegfilgrastim was well tolerated. The duration of severe neutropenia and the incidence of febrile neutropenia after pegfilgrastim and filgrastim were comparable. By using pegfilgrastim, the number of subcutaneous injections could be reduced to one single injection per cycle.
引用
收藏
页码:449 / 451
页数:3
相关论文
共 15 条
[1]   Long-term follow-up of normal peripheral blood progenitor cell donors treated with filgrastim:: no evidence of increased risk of leukemia development [J].
Anderlini, P ;
Chan, FA ;
Champlin, RE ;
Körbling, M ;
Strom, SS .
BONE MARROW TRANSPLANTATION, 2002, 30 (10) :661-663
[2]  
Bence Aimee K, 2002, J Am Pharm Assoc (Wash), V42, P806, DOI 10.1331/108658002764653595
[3]   REDUCTION BY GRANULOCYTE COLONY-STIMULATING FACTOR OF FEVER AND NEUTROPENIA INDUCED BY CHEMOTHERAPY IN PATIENTS WITH SMALL-CELL LUNG-CANCER [J].
CRAWFORD, J ;
OZER, H ;
STOLLER, R ;
JOHNSON, D ;
LYMAN, G ;
TABBARA, I ;
KRIS, M ;
GROUS, J ;
PICOZZI, V ;
RAUSCH, G ;
SMITH, R ;
GRADISHAR, W ;
YAHANDA, A ;
VINCENT, M ;
STEWART, M ;
GLASPY, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (03) :164-170
[4]   A randomized double-blind multicenter phase III study of fixed-dose single-administration pegfilgrastim versus daily filgrastim in patients receiving myelosuppressive chemotherapy [J].
Green, MD ;
Koelbl, H ;
Baselga, J ;
Galid, A ;
Guillem, V ;
Gascon, P ;
Siena, S ;
Lalisang, RI ;
Samonigg, H ;
Clemens, MR ;
Zani, V ;
Liang, BC ;
Renwick, J ;
Piccart, MJ .
ANNALS OF ONCOLOGY, 2003, 14 (01) :29-35
[6]   Blinded, randomized, multicenter study to evaluate single administration pegfilgrastim once per cycle versus daily filgrastim as an adjunct to chemotherapy in patients with high-risk stage II or stage III/IV breast cancer [J].
Holmes, FA ;
O'Shaughnessy, JA ;
Vukelja, S ;
Jones, SE ;
Shogan, J ;
Savin, M ;
Glaspy, J ;
Moore, M ;
Meza, L ;
Wiznitzer, I ;
Neumann, TA ;
Hill, LR ;
Liang, BC .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (03) :727-731
[7]   Randomized, dose-escalation study of SD/01 compared with daily filgrastim in patients receiving chemotherapy [J].
Johnston, E ;
Crawford, J ;
Blackwell, S ;
Bjurstrom, T ;
Lockbaum, P ;
Roskos, L ;
Yang, BB ;
Gardner, S ;
Miller-Messana, MA ;
Shoemaker, D ;
Garst, J ;
Schwab, G .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (13) :2522-2528
[8]  
Kubista Ernst, 2003, Clin Breast Cancer, V3, P391, DOI 10.3816/CBC.2003.n.003
[9]  
Kushner BH, 2000, CANCER-AM CANCER SOC, V89, P2122, DOI 10.1002/1097-0142(20001115)89:10<2122::AID-CNCR13>3.0.CO
[10]  
2-K