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Article: Combination therapy with oncolytic viruses and immune checkpoint inhibitors

TitleCombination therapy with oncolytic viruses and immune checkpoint inhibitors
Authors
KeywordsCancer
combination treatment
immune checkpoint inhibitors
immunotherapy
oncolytic viruses
Issue Date2020
Citation
Expert Opinion on Biological Therapy, 2020, v. 20, n. 6, p. 635-652 How to Cite?
AbstractIntroduction: Immune checkpoint inhibitors (ICI) have dramatically improved the outcome for cancer patients across multiple tumor types. However the response rates to ICI monotherapy remain relatively low, in part due to some tumors cultivating an inherently ‘cold’ immune microenvironment. Oncolytic viruses (OV) have the capability to promote a ‘hotter’ immune microenvironment which can improve the efficacy of ICI. Areas covered: In this article we conducted a literature search through Pubmed/Medline to identify relevant articles in both the pre-clinical and clinical settings for combining OVs with ICIs and discuss the impact of this approach on treatment as well as changes within the tumor microenvironment. We also explore the future directions of this novel combination strategy. Expert opinion: The imminent results of the Phase 3 study combining pembrolizumab with or without T-Vec injection are eagerly awaited. OV/ICI combinations remain one of the most promising avenues to explore in the success of cancer immunotherapy.
Persistent Identifierhttp://hdl.handle.net/10722/334657
ISSN
2021 Impact Factor: 5.589
2020 SCImago Journal Rankings: 1.088

 

DC FieldValueLanguage
dc.contributor.authorChiu, Matthew-
dc.contributor.authorArmstrong, Edward John Lloyd-
dc.contributor.authorJennings, Vicki-
dc.contributor.authorFoo, Shane-
dc.contributor.authorCrespo-Rodriguez, Eva-
dc.contributor.authorBozhanova, Galabina-
dc.contributor.authorPatin, Emmanuel Christian-
dc.contributor.authorMcLaughlin, Martin-
dc.contributor.authorMansfield, David-
dc.contributor.authorBaker, Gabriella-
dc.contributor.authorGrove, Lorna-
dc.contributor.authorPedersen, Malin-
dc.contributor.authorKyula, Joan-
dc.contributor.authorRoulstone, Victoria-
dc.contributor.authorWilkins, Anna-
dc.contributor.authorMcDonald, Fiona-
dc.contributor.authorHarrington, Kevin-
dc.contributor.authorMelcher, Alan-
dc.date.accessioned2023-10-20T06:49:42Z-
dc.date.available2023-10-20T06:49:42Z-
dc.date.issued2020-
dc.identifier.citationExpert Opinion on Biological Therapy, 2020, v. 20, n. 6, p. 635-652-
dc.identifier.issn1471-2598-
dc.identifier.urihttp://hdl.handle.net/10722/334657-
dc.description.abstractIntroduction: Immune checkpoint inhibitors (ICI) have dramatically improved the outcome for cancer patients across multiple tumor types. However the response rates to ICI monotherapy remain relatively low, in part due to some tumors cultivating an inherently ‘cold’ immune microenvironment. Oncolytic viruses (OV) have the capability to promote a ‘hotter’ immune microenvironment which can improve the efficacy of ICI. Areas covered: In this article we conducted a literature search through Pubmed/Medline to identify relevant articles in both the pre-clinical and clinical settings for combining OVs with ICIs and discuss the impact of this approach on treatment as well as changes within the tumor microenvironment. We also explore the future directions of this novel combination strategy. Expert opinion: The imminent results of the Phase 3 study combining pembrolizumab with or without T-Vec injection are eagerly awaited. OV/ICI combinations remain one of the most promising avenues to explore in the success of cancer immunotherapy.-
dc.languageeng-
dc.relation.ispartofExpert Opinion on Biological Therapy-
dc.subjectCancer-
dc.subjectcombination treatment-
dc.subjectimmune checkpoint inhibitors-
dc.subjectimmunotherapy-
dc.subjectoncolytic viruses-
dc.titleCombination therapy with oncolytic viruses and immune checkpoint inhibitors-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1080/14712598.2020.1729351-
dc.identifier.pmid32067509-
dc.identifier.scopuseid_2-s2.0-85084271136-
dc.identifier.volume20-
dc.identifier.issue6-
dc.identifier.spage635-
dc.identifier.epage652-
dc.identifier.eissn1744-7682-

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