TNFerade biologic, an adenovector with a radiation-inducible, promoter, carrying the human tumor necrosis factor alpha gene: A phase I study in patients with solid tumors

被引:153
作者
Senzer, N
Mani, S
Rosemurgy, A
Nemunaitis, J
Cunningham, C
Guha, C
Bayol, N
Gillen, M
Chu, K
Rasmussen, C
Rasmussen, H
Kufe, D
Weichselbaum, R
Hanna, N [1 ]
机构
[1] Univ Kentucky, Med Ctr, Dept Gen Surg, Lexington, KY USA
[2] Univ Chicago, Med Ctr, Chicago, IL 60637 USA
[3] Dana Farber Canc Inst, Dept Med, Boston, MA 02115 USA
[4] GenVec Inc, Gaithersburg, MD USA
[5] Univ S Florida, Tampa, FL 33612 USA
[6] Albert Einstein Coll Med, Bronx, NY 10467 USA
[7] US Oncol, Dallas, TX USA
关键词
D O I
10.1200/JCO.2004.01.227
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose TNFerade is a replication deficient adenovector that expresses human tumor necrosis factor alpha under control of the radiation-inducible Egr-1 promoter. The goals of this study were to determine the safety and toxicity of TNFerade in combination with radiation therapy. Patients and Methods TNFerade,was administered by intratumoral administration, weekly for 6 weeks with concomitant radiation (30 to 70 Gy). Seven dose levels were studied (4 X 10(7) particle units [pu] to 4 X 10(11) pu) in patients with solid tumors being treated with radiation. Results Thirty-six patients were assessable for toxicity and 30 for tumor response. Most frequent TNFerade-related toxicities were fever (22%), injection site pain (19%), and chills (19%). No dose-limiting toxicities were observed. Overall, 21 of 30 patients (70%) demonstrated objective tumor response (five complete responses, nine partial responses, and seven minimal responses). In four of five patients with synchronous lesions, a differential response between lesions treated with TNFerade + radiation compared with radiation only was observed. Conclusion This is the first human study with TNFerade and radiation. The integrated treatment was well tolerated in patients with predominantly prior treatment-refractory solid tumors. Controlled prospective clinical trials have been initiated to more fully define the therapeutic contribution of TNFerade. (C) 2004 by American Society of Clinical Oncology.
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页码:592 / 601
页数:10
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