Intratumoral interleukin 2 for renal-cell carcinoma by direct gene transfer of a plasmid DNA/DMRIE/DOPE lipid complex

被引:26
作者
Hoffman, DMJ [1 ]
Figlin, RA [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Med,Jonsson Comprehens Canc Ctr, Div Hematol Oncol, Los Angeles, CA 90095 USA
关键词
D O I
10.1007/s003450050189
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Metastatic renal-cell carcinoma (RCC) is not responsive to conventional cytotoxic chemotherapy, but a subset of patients achieve a durable remission with the use of interleukin-2 (IL-2). IL-2 is currently the only Food and Drug Administration (FDA)-approved treatment for metastatic RCC, and it benefits 10-20% of those who receive it. However, it is accompanied by significant, occasionally life-threatening toxicity. Attempts to maintain the efficacy of IL-2 while minimizing systemic side effects have led to the development of IL-2 gene therapies. Leuvectin is a plasmid DNA/lipid com Flex composed of a plasmid DNA expression vector (VCL-1102, 30) encoding human IL-2 complexed in a 5:1 mass ratio with DMRIE/DOPE lipid (1,2-dimyristyloxypropyl-3-dimethylhydroxyethyl ammonium bromide/ dioleoylphosphatidyl ethanolamine), which has been developed for the treatment of malignancy. DMRIE/DOPE is a cationic lipid that has been shown to facilitate in vitro transfection of plasmid DNA. It has been demonstrated that in vitro transfection with the IL-2 plasmid DNA/DMRIE/DOPE complex results in the expression of sustained levels of biologically active IL-2. Established human tumor cell lines and primary human tumor cells obtained from biopsies are readily transfected in vitro. resulting in the expression of IL-2. Following in vitro transfection, IL-2 expression has been Found to persist for up to several weeks in primary tumor cells. In preclinical efficacy studies in a murine model of renal-cell carcinoma the direct intratumoral administration of an IL-2 plasmid DNA/DMRIE/ DOPE complex resulted in complete tumor regression in the majority of mice. In preclinical animal-safety studies, repeated administration of Leuvectin was safe and well tolerated. Following these promising preclinical trials, Leuvectin has been taken into clinical trial. The results of two early studies indicate that Leuvectin is safe, is free of systemic toxicity, and has biologic activity.
引用
收藏
页码:152 / 156
页数:5
相关论文
共 45 条
[1]   TRANSDUCTION OF HUMAN-MELANOMA CELLS WITH INTERLEUKIN-2 GENE REDUCES TUMORIGENICITY AND ENHANCES HOST ANTITUMOR IMMUNITY - A NUDE-MOUSE MODEL [J].
ABDELWAHAB, Z ;
LI, WP ;
OSANTO, S ;
DARROW, TL ;
HESSLING, J ;
VERVAERT, CE ;
BURRASCANO, M ;
BARBER, J ;
SEIGLER, HF .
CELLULAR IMMUNOLOGY, 1994, 159 (01) :26-39
[2]   INTRATUMORAL INJECTION OF AN ADENOVIRUS EXPRESSING INTERLEUKIN-2 INDUCES REGRESSION AND IMMUNITY IN A MURINE BREAST-CANCER MODEL [J].
ADDISON, CL ;
BRACIAK, T ;
RALSTON, R ;
MULLER, WJ ;
GAULDIE, J ;
GRAHAM, FL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) :8522-8526
[3]  
Bukowski RM, 1997, CANCER-AM CANCER SOC, V80, P1198, DOI 10.1002/(SICI)1097-0142(19971001)80:7<1198::AID-CNCR3>3.0.CO
[4]  
2-H
[5]  
Cao X, 1996, GENE THER, V3, P421
[6]   PHASE-I STUDY OF TRANSFECTED CANCER-CELLS EXPRESSING THE INTERLEUKIN-2 GENE-PRODUCT IN LIMITED STAGE SMALL-CELL LUNG-CANCER [J].
CASSILETH, PA ;
PODACK, E ;
SRIDHAR, K ;
SAVARAJ, N ;
HANLON, J .
HUMAN GENE THERAPY, 1995, 6 (03) :369-383
[7]  
CORDIER L, 1995, GENE THER, V2, P16
[8]   PRODUCTION OF TUMOR-NECROSIS-FACTOR-ALPHA AND INTERFERON GAMMA IN INTERLEUKIN-2-TREATED MELANOMA PATIENTS - CORRELATION WITH CLINICAL TOXICITY [J].
ECONOMOU, JS ;
HOBAN, M ;
LEE, JD ;
ESSNER, R ;
SWISHER, S ;
MCBRIDE, W ;
HOON, DB ;
MORTON, DL .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1991, 34 (01) :49-52
[9]  
Egilmez NK, 1996, GENE THER, V3, P607
[10]  
ETTINGHAUSEN SE, 1987, BLOOD, V69, P1654