Molecular and traditional chemotherapy: A united front against prostate cancer |
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Authors: | P. Singh M. Yam P.J. Russell A. Khatri |
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Affiliation: | 1. Oncology Research Centre, Prince of Wales Hospital, Randwick, Sydney, NSW 2031, Australia;2. Faculty of Medicine, University of New South Wales, Kensington, NSW 2036, Australia;3. Centre for Medicine and Oral Health, Griffith University – Gold Coast GH1, High Street, Southport, Gold Coast, QLD 4215, Australia;4. Australian Prostate Cancer Research Centre – Queensland, Princess Alexandra Hospital, Woollangabba, QLD, Australia;5. Institute of Health and Biomedical Innovation, Queensland University of Technology, 60 Musk Avenue, Kelvin Grove, QLD 4059, Australia |
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Abstract: | ![]() Castrate resistant prostate cancer (CRPC) is essentially incurable. Recently though, chemotherapy demonstrated a survival benefit (∼2 months) in the treatment of CRPC. While this was a landmark finding, suboptimal efficacy and systemic toxicities at the therapeutic doses warranted further development. Smart combination therapies, acting through multiple mechanisms to target the heterogeneous cell populations of PC and with potential for reduction in individual dosing, need to be developed. In that, targeted molecular chemotherapy has generated significant interest with the potential for localized treatment to generate systemic efficacy. This can be further enhanced through the use of oncolytic conditionally replicative adenoviruses (CRAds) to deliver molecular chemotherapy. The prospects of chemotherapy and molecular-chemotherapy as single and as components of combination therapies are discussed. |
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Keywords: | Chemotherapy Docetaxel Molecular chemotherapy Purine nucleoside phosphorylase Gene directed pro-drug enzyme therapy Conditionally replicating adenovirus |
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