scholarly journals Virotherapy: cancer gene therapy at last?

F1000Research ◽  
2016 ◽  
Vol 5 ◽  
pp. 2105 ◽  
Author(s):  
Alan E. Bilsland ◽  
Pavlina Spiliopoulou ◽  
T. R. Jeffry Evans

For decades, effective cancer gene therapy has been a tantalising prospect; for a therapeutic modality potentially able to elicit highly effective and selective responses, definitive efficacy outcomes have often seemed out of reach. However, steady progress in vector development and accumulated experience from previous clinical studies has finally led the field to its first licensed therapy. Following a pivotal phase III trial, Imlygic (talimogene laherparepvec/T-Vec) received US approval as a treatment for cutaneous and subcutaneous melanoma in October 2015, followed several weeks later by its European authorisation. These represent the first approvals for an oncolytic virotherapy. Imlygic is an advanced-generation herpesvirus-based vector optimised for oncolytic and immunomodulatory activities. Many other oncolytic agents currently remain in development, providing hope that current success will be followed by other diverse vectors that may ultimately come to constitute a new class of clinical anti-cancer agents. In this review, we discuss some of the key oncolytic viral agents developed in the adenovirus and herpesvirus classes, and the prospects for further enhancing their efficacy by combining them with novel immunotherapeutic approaches.

2019 ◽  
Vol 154 ◽  
pp. 231-232 ◽  
Author(s):  
R. Shapira-Frommer ◽  
I. Barshack ◽  
Y.C. Cohen ◽  
T. Rachmilewitz Minei ◽  
N. Yakov ◽  
...  

2005 ◽  
Vol 4 (4) ◽  
pp. 315-330 ◽  
Author(s):  
Masato Yamamoto ◽  
David T. Curiel

The prognosis of patients with some kinds of cancers whose patients are often found unresectable upon diagnosis is still dismal. In these fields, development of a new therapeutic modality is needed and gene therapy represents one promising strategy. So far, numerous cancer gene therapy clinical trials based on these principles have been carried out and have shown the safety of such modalities, but have fallen short of the initial expectations to cure cancers. In this review, we would like to make a problem-oriented discussion of current status of cancer gene therapy research by using mainly gastrointestinal cancers as an example. In order to overcome obstacles for full realization of cancer gene therapy, numerous researches have been conducted by many researchers. Various cancer-selective and non-selective genes, as well as lytic viruses themselves have been employed for gene therapy. In the context of gene delivery method, different kinds of viral and non-viral strategies have been utilized. In addition, surrogate assays, such as soluble markers and imaging, have been developed for safer and more informative clinical trials. Many experiments and clinical trials to date have figured out current obstacles for the realization of an effective cancer gene therapy modality. Tireless efforts to overcome such hurdles and continuous infusion of novel concepts into this field should lead to break through technologies and the cure of the patients.


1999 ◽  
Vol 74 (2) ◽  
pp. 227-234 ◽  
Author(s):  
Timothy J. Vanderkwaak ◽  
Minghui Wang ◽  
Jesús Gómez-Navarro ◽  
Claudine Rancourt ◽  
Igor Dmitriev ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document