Virus directed enzyme prodrug therapy: Intratumoural administration of a replication-deficient adenovirus encoding nitroreductase to patients with resectable liver cancer

Research output: Contribution to journalArticle

Authors

  • Darius Mirza
  • S Oliff
  • W Gerritsen
  • JR van der Sijp
  • Gary Reynolds
  • Sarah Bonney
  • R Rajaratnam
  • Diana Hull
  • M Horne
  • J Ellis
  • Andrew Mountain
  • PA Harris
  • Lawrence Young
  • Nicholas James
  • DJ Kerr

Abstract

Purpose Virus-directed enzyme prodrug therapy depends on selective delivery of virus encoding a prodrug-activating enzyme to tumor, followed by systemic treatment with prodrug to achieve high levels of the activated cytotoxic at the intended site of action. The use of the bacterial enzyme nitroreductase to activate CB1954 (5-(aziridin-1-yl)-2,4-dinitrobenzamide) to a short lived, highly toxic DNA cross-linking agent has been demonstrated in tumor xenografts. In this study, we report the first clinical trial investigating the feasibility, safety, and transgene expression of a replication-defective adenovirus encoding nitroreductase (CTL102) in patients with liver tumors. Patients and Methods Patients with resectable primary or secondary (colorectal) liver cancer received a single dose of CTL102 delivered by direct intratumoral inoculation 3 to 8 days before surgical resection. Results Eighteen patients were treated with escalating doses of CTL102 (range, 10(8)-5 X 10(11) virus particles). The vector was well tolerated with minimal side effects, had a short half-life in the circulation, and stimulated a robust antibody response. Dose-related increases in tumoral nitroreductase expression measured by immunohistochemical analysis have been observed. Conclusion Direct intratumoral inoculation of CTL102 to patients with primary and secondary liver cancer is feasible and well tolerated. The high level of nitroreductase expression observed at 1 to 5 X 10(11) virus particles mandates further studies in patients with inoperable tumors who will receive CTL102 and CB1954.

Details

Original languageEnglish
Pages (from-to)1546-1552
Number of pages7
JournalJournal of Clinical Oncology
Volume22
Early online date29 Mar 2004
Publication statusPublished - 29 Mar 2004