Novel effects with polyethylene glycol modified pharmaceuticals

被引:39
作者
Yowell, SL
Blackwell, S
机构
[1] Duke Univ, Med Ctr, Dept Pharm, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Thorac Oncol Program, Durham, NC 27710 USA
关键词
pegylation; oncology; pegfilgrastim; pegylated liposomal doxorubicin;
D O I
10.1016/S0305-7372(02)80002-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Proteins undergo extensive hydrolysis in the gastrointestinal tract and have short circulating half-lives in the blood, For optimal clinical efficacy, therefore, they must be given by daily injections. Attaching a polyethylene glycol (PEG) moiety (pegylation) improves the pharmacokinetic and pharmacodynamic profiles of proteins. Pegfilgrastim (pegylated filgrastim) has a longer halflife than unmodified filgrastim and, when administered as a single dose, has been shown to be at least as efficacious as daily filgrastim. Because of its reduced renal clearance, the elimination of pegfilgrastim is predominantly neutrophil-mediated, so its clearance is self-regulated. In addition, pegfilgrastim can be administered at a fixed dose instead of in weight-based doses, For these reasons, pegfilgrastim can potentially increase patient adherence and acceptance of treatment, thus having a beneficial effect on their quality of life. Furthermore, treatment is likely to cost less because of the reduced need for medical interventions. Similarly, pegylated liposomal doxorubicin has a longer half-life than unmodified doxorubicin and has been shown, because of its reduced reticuloendothelial system clearance, to produce higher concentrations of doxorubicin in tumours and to have greater clinical efficacy than doxorubicin in the treatment of some solid tumours. Pegylated liposomal doxorubicin is also associated with less myelosuppression and febrile neutropenia. (C) 2002 Elsevier Science. All rights reserved.
引用
收藏
页码:3 / 6
页数:4
相关论文
共 16 条
[1]   Polyethylene glycol-conjugated pharmaceutical proteins [J].
Bailon, P ;
Berthold, W .
PHARMACEUTICAL SCIENCE & TECHNOLOGY TODAY, 1998, 1 (08) :352-356
[2]   Polyethylene glycol-liposomal doxorubicin - A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in the management of AIDS-related Kaposi's sarcoma [J].
Coukell, AJ ;
Spencer, CM .
DRUGS, 1997, 53 (03) :520-538
[3]   Clinical uses of pegylated pharmaceuticals in oncology [J].
Crawford, J .
CANCER TREATMENT REVIEWS, 2002, 28 :7-11
[4]  
FISHER M, 2001, CURR TRENDS CYTOKINE, V1, P2
[5]   FILGRASTIM - A REVIEW OF ITS PHARMACOLOGICAL PROPERTIES AND THERAPEUTIC EFFICACY IN NEUTROPENIA [J].
FRAMPTON, JE ;
LEE, CR ;
FAULDS, D .
DRUGS, 1994, 48 (05) :731-760
[6]   Development of liposomal anthracyclines: from basics to clinical applications [J].
Gabizon, A ;
Goren, D ;
Cohen, R ;
Barenholz, Y .
JOURNAL OF CONTROLLED RELEASE, 1998, 53 (1-3) :275-279
[7]   Polyethylene glycol coated (pegylated) liposomal doxorubicin - Rationale for use in solid tumours [J].
Gabizon, A ;
Martin, F .
DRUGS, 1997, 54 (Suppl 4) :15-21
[8]  
GREEN M, 2001, P AN M AM SOC CLIN, V20, pA23
[9]  
HOLMES FA, 2000, 23 ANN SAN ANT BREAS
[10]   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