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Two roads for oncolytic immunotherapy development
Oncolytic viruses are an emerging class of immunotherapy agents for cancer treatment. In this issue of JITC, Machiels et al. reports early phase data from an oncolytic adenovirus given by intravenous (IV) administration. While this may allow easy access to metastatic lesions, there is limited data s...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359832/ https://www.ncbi.nlm.nih.gov/pubmed/30709365 http://dx.doi.org/10.1186/s40425-019-0515-2 |
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author | Kaufman, Howard L. Bommareddy, Praveen K. |
author_facet | Kaufman, Howard L. Bommareddy, Praveen K. |
author_sort | Kaufman, Howard L. |
collection | PubMed |
description | Oncolytic viruses are an emerging class of immunotherapy agents for cancer treatment. In this issue of JITC, Machiels et al. reports early phase data from an oncolytic adenovirus given by intravenous (IV) administration. While this may allow easy access to metastatic lesions, there is limited data supporting the therapeutic effectiveness of this approach. Further studies should include assessment of viral replication in tumor tissue and consider comparative trials using IV and intratumoral delivery to fully optimize oncolytic immunotherapy. |
format | Online Article Text |
id | pubmed-6359832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63598322019-02-07 Two roads for oncolytic immunotherapy development Kaufman, Howard L. Bommareddy, Praveen K. J Immunother Cancer Commentary Oncolytic viruses are an emerging class of immunotherapy agents for cancer treatment. In this issue of JITC, Machiels et al. reports early phase data from an oncolytic adenovirus given by intravenous (IV) administration. While this may allow easy access to metastatic lesions, there is limited data supporting the therapeutic effectiveness of this approach. Further studies should include assessment of viral replication in tumor tissue and consider comparative trials using IV and intratumoral delivery to fully optimize oncolytic immunotherapy. BioMed Central 2019-02-01 /pmc/articles/PMC6359832/ /pubmed/30709365 http://dx.doi.org/10.1186/s40425-019-0515-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Commentary Kaufman, Howard L. Bommareddy, Praveen K. Two roads for oncolytic immunotherapy development |
title | Two roads for oncolytic immunotherapy development |
title_full | Two roads for oncolytic immunotherapy development |
title_fullStr | Two roads for oncolytic immunotherapy development |
title_full_unstemmed | Two roads for oncolytic immunotherapy development |
title_short | Two roads for oncolytic immunotherapy development |
title_sort | two roads for oncolytic immunotherapy development |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359832/ https://www.ncbi.nlm.nih.gov/pubmed/30709365 http://dx.doi.org/10.1186/s40425-019-0515-2 |
work_keys_str_mv | AT kaufmanhowardl tworoadsforoncolyticimmunotherapydevelopment AT bommareddypraveenk tworoadsforoncolyticimmunotherapydevelopment |