Doxorubicin and irinotecan drug-eluting beads for treatment of glioma: a pilot study in a rat model

被引:27
作者
Baltes, Steffen [1 ]
Freund, Ina [1 ]
Lewis, Andrew L. [2 ]
Nolte, Ingo [3 ]
Brinker, Thomas [1 ]
机构
[1] Int Neurosci Inst GmbH, D-30625 Hannover, Germany
[2] Biocompatibles UK Ltd, Surrey GU9 8QL, England
[3] Univ Vet Med Hannover, Hannover, Germany
关键词
PEGYLATED LIPOSOMAL DOXORUBICIN; CONVECTION-ENHANCED DELIVERY; TOPOISOMERASE-I INHIBITOR; RECURRENT MALIGNANT GLIOMA; BRAIN-TUMOR XENOGRAFTS; LOCAL-DELIVERY; 5-FLUOROURACIL-LOADED MICROSPHERES; TRANSARTERIAL CHEMOEMBOLIZATION; THERAPEUTIC-EFFICACY; ETHYL-NITROSOUREA;
D O I
10.1007/s10856-009-3803-4
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Despite some progress in therapy, the prognosis of patients with malignant gliomas remains poor. Local delivery of cytostatics to the tumour has been proven to be an efficacious therapeutic approach but which nevertheless needs further improvements. Drug Eluting Beads (DEB), have been developed as drug delivery embolisation systems for use in trans-arterial chemoembolisation. We tested in a rat model of malignant glioma, whether DEB, loaded with doxorubicin or irinotecan, may be used for local treatment of brain tumours. Unloaded and drug loaded DEB were implanted into the brains of healthy and tumour bearing BD IX rats followed by histological investigations and survival assessment. Intracerebral implantation of unloaded DEB caused no significant local tissue damage, whilst both doxorubicin and irinotecan DEB improved survival time significantly. However, a significant local toxicity was found after the implantation of doxorubicin DEB but not with irinotecan DEB. We concluded that irinotecan appears to be superior in terms of the risk-benefit ratio and that DEB may be used for local treatment of brain tumours.
引用
收藏
页码:1393 / 1402
页数:10
相关论文
共 46 条
[1]
Chakravarti Arnab, 2008, P173
[2]
INDUCTION OF NEUROGENIC MALIGNANCIES BY ONE SINGLE DOSE OF ETHYL-NITROSOUREA (ENU) GIVEN TO NEWBORN AND JUVENILE BD IX-STRAIN RATS [J].
DRUCKREY, H ;
SCHAGEN, B ;
IVANKOVIC, S .
ZEITSCHRIFT FUR KREBSFORSCHUNG, 1970, 74 (02) :141-+
[3]
TRANSPLACENTAL INDUCTION OF MALIGNANT TUMOURS OF NERVOUS SYSTEM .2. ETHYL-NITROSOUREA IN 10 GENETICALLY DEFINED STRAINS OF RATS [J].
DRUCKREY, H ;
LANDSCHUTZ, C ;
IVANKOVIC, S .
ZEITSCHRIFT FUR KREBSFORSCHUNG, 1970, 73 (04) :371-+
[4]
Chemoembolisation of rat colorectal liver metastases with drug eluting beads loaded with irinotecan or doxorubicin [J].
Eyol, Erguel ;
Boleij, Annemarie ;
Taylor, Rachel R. ;
Lewis, Andrew L. ;
Berger, Martin R. .
CLINICAL & EXPERIMENTAL METASTASIS, 2008, 25 (03) :273-282
[5]
Fiorentini G, 2007, IN VIVO, V21, P1085
[6]
Therapeutic efficacy study of novel 5-FU-loaded PMM 2.1.2-based microspheres on C6 glioma [J].
Fournier, E ;
Passirani, C ;
Vonarbourg, A ;
Lemaire, L ;
Colin, N ;
Sagodira, S ;
Menei, P ;
Benoit, JP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 268 (1-2) :31-35
[7]
Therapeutic effectiveness of novel 5-fluorouracil-loaded poly(methylidene malonate 2.1.2)-based microspheres on F98 glioma-bearing rats [J].
Fournier, E ;
Passirani, C ;
Montero-Menei, C ;
Colin, N ;
Breton, P ;
Sagodira, S ;
Menei, P ;
Benoit, JP .
CANCER, 2003, 97 (11) :2822-2829
[8]
In vitro drug response and molecular markers associated with drug resistance in malignant gliomas [J].
Fruehauf, John P. ;
Brem, Henry ;
Brem, Steven ;
Sloan, Andrew ;
Barger, Geoffrey ;
Huang, Weidong ;
Parker, Ricardo .
CLINICAL CANCER RESEARCH, 2006, 12 (15) :4523-4532
[9]
Garside R, 2007, Health Technol Assess, V11, piii
[10]
Gilbert MR, 2003, CLIN CANCER RES, V9, P2940