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Volume 21, Issue 2, Pages 91-98 (April 2010)


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Clinical trials with oncolytic reovirus: Moving beyond phase I into combinations with standard therapeutics

K.J. HarringtonaCorresponding Author Informationemail address, R.G. Vileb, A. Melcherc, J. Chesterc, H.S. Pandhad

published online 11 March 2010.

Abstract 

It is time for those working on oncolytic viruses to take stock of the status of the field. We now have at our disposal an array of potential therapeutic agents, and are beginning to conduct early-phase clinical trials in patients with relapsed/metastatic cancers. By drawing on lessons learned during the development of other biological therapies, such as monoclonal antibodies and targeted small molecule inhibitors, we are now in a position to chart the course of the next wave of trials that will go beyond the phase I studies of safety and feasibility. In this article we review our approach to the development of oncolytic viruses as cancer therapeutics. In doing so, we emphasise the fact that this process is modular and involves multiple iterative steps between the laboratory and the clinic. Ultimately, at least in the medium term, the future of oncolytic virotherapy lies in combination regimens with standard anti-cancer agents such as radiation and chemotherapy.

a The Institute of Cancer Research, Chester Beatty Laboratories, Targeted Therapy Laboratory, 237 Fulham Road, London SW3 6JB, UK

b Molecular Medicine Program, Mayo Clinic, Rochester, MN, USA

c Leeds Institute of Molecular Medicine, Leeds, UK

d The University of Surrey, Guildford, UK

Corresponding Author InformationCorresponding author. Tel.: +44 020 7153 5157; fax: +44 020 7808 2235.

PII: S1359-6101(10)00017-1

doi:10.1016/j.cytogfr.2010.02.006


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