The Current Status and Future Prospects of Oncolytic Viruses in Clinical Trials against Melanoma, Glioma, Pancreatic, and Breast Cancers.
The Current Status and Future Prospects of Oncolytic Viruses in Clinical Trials against Melanoma, Glioma, Pancreatic, and Breast Cancers.
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DOI:
10.3390/cancers10100356
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发表时间:
2018-09-26
期刊:
影响因子:
5.2
通讯作者:
Kasuya H
中科院分区:
文献类型:
--
作者:
Eissa IR;Bustos-Villalobos I;Ichinose T;Matsumura S;Naoe Y;Miyajima N;Morimoto D;Mukoyama N;Zhiwen W;Tanaka M;Hasegawa H;Sumigama S;Aleksic B;Kodera Y;Kasuya H
Oncolytic viral therapy has been accepted as a standard immunotherapy since talimogene laherparepvec (T-VEC, Imlygic®) was approved by the Food and Drug Administration (FDA) and European Medicines Agency (EMA) for melanoma treatment in 2015. Various oncolytic viruses (OVs), such as HF10 (Canerpaturev—C-REV) and CVA21 (CAVATAK), are now actively being developed in phase II as monotherapies, or in combination with immune checkpoint inhibitors against melanoma. Moreover, in glioma, several OVs have clearly demonstrated both safety and a promising efficacy in the phase I clinical trials. Additionally, the safety of several OVs, such as pelareorep (Reolysin®), proved their safety and efficacy in combination with paclitaxel in breast cancer patients, but the outcomes of OVs as monotherapy against breast cancer have not provided a clear therapeutic strategy for OVs. The clinical trials of OVs against pancreatic cancer have not yet demonstrated efficacy as either monotherapy or as part of combination therapy. However, there are several oncolytic viruses that have successfully proved their efficacy in different preclinical models. In this review, we mainly focused on the oncolytic viruses that transitioned into clinical trials against melanoma, glioma, pancreatic, and breast cancers. Hence, we described the current status and future prospects of OVs clinical trials against melanoma, glioma, pancreatic, and breast cancers.
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影响因子:
4.7
作者:
Eissa IR;Naoe Y;Bustos-Villalobos I;Ichinose T;Tanaka M;Zhiwen W;Mukoyama N;Morimoto T;Miyajima N;Hitoki H;Sumigama S;Aleksic B;Kodera Y;Kasuya H
通讯作者:
Kasuya H
DOI:
10.1016/j.ymthe.2017.08.016
发表时间:
2017-12-06
期刊:
Molecular therapy : the journal of the American Society of Gene Therapy
影响因子:
--
作者:
Geletneky K;Hajda J;Angelova AL;Leuchs B;Capper D;Bartsch AJ;Neumann JO;Schöning T;Hüsing J;Beelte B;Kiprianova I;Roscher M;Bhat R;von Deimling A;Brück W;Just A;Frehtman V;Löbhard S;Terletskaia-Ladwig E;Fry J;Jochims K;Daniel V;Krebs O;Dahm M;Huber B;Unterberg A;Rommelaere J
通讯作者:
Rommelaere J
影响因子:
3.8
作者:
Bernstein, V.;Ellard, S. L.;Seymour, L.
通讯作者:
Seymour, L.
影响因子:
12.4
作者:
Galanis, Evanthia;Markovic, Svetomir N.;Kendra, Kari
通讯作者:
Kendra, Kari
影响因子:
45.3
作者:
Chesney, Jason;Puzanov, Igor;Kaufman, Howard L.
通讯作者:
Kaufman, Howard L.