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肺癌的免疫治疗临床研究进展
Lung cancer is a highly malignant disease with poor prognosis, most cases are diagnosed at a very late stage. More effective medications or therapies should be developed to improve its prognosis. The advancement of tumor immunity and tumor immunosuppression facilitated the feasibility of immunothera...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
Publicado: |
中国肺癌杂志编辑部
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999828/ https://www.ncbi.nlm.nih.gov/pubmed/23075686 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.10.08 |
_version_ | 1783331523205791744 |
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collection | PubMed |
description | Lung cancer is a highly malignant disease with poor prognosis, most cases are diagnosed at a very late stage. More effective medications or therapies should be developed to improve its prognosis. The advancement of tumor immunity and tumor immunosuppression facilitated the feasibility of immunotherapies for lung cancer. Ipilimumab, antibody to Programmed death-1 (PD-1), Toll-like receptor agonists, liposomal BLP25 (L- BLP25), belagenpumatucel-L, melanoma-associated antigen A3 (MAGE-A3) vaccine and talactoferrin have been proved to be effective for lung cancer through early clinical trials, most of the drugs have moved forward to Phase Ⅲ trials, so as to collect much higher level evidence to support the immunotherapies incorporated into the multidisciplinary treatment of lung cancer. The selection of target patients at appropriate stages, breaking down of tumor immunosuppression as well as the objective measurement of tumor response to the therapy are major challenges for the development of immunotherapies for lung cancer. The clarifying of the mechanism of immune escape led to the above drug development, and immune-senescence has already become the hotspot in this field. |
format | Online Article Text |
id | pubmed-5999828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | 中国肺癌杂志编辑部 |
record_format | MEDLINE/PubMed |
spelling | pubmed-59998282018-07-06 肺癌的免疫治疗临床研究进展 Zhongguo Fei Ai Za Zhi 综述 Lung cancer is a highly malignant disease with poor prognosis, most cases are diagnosed at a very late stage. More effective medications or therapies should be developed to improve its prognosis. The advancement of tumor immunity and tumor immunosuppression facilitated the feasibility of immunotherapies for lung cancer. Ipilimumab, antibody to Programmed death-1 (PD-1), Toll-like receptor agonists, liposomal BLP25 (L- BLP25), belagenpumatucel-L, melanoma-associated antigen A3 (MAGE-A3) vaccine and talactoferrin have been proved to be effective for lung cancer through early clinical trials, most of the drugs have moved forward to Phase Ⅲ trials, so as to collect much higher level evidence to support the immunotherapies incorporated into the multidisciplinary treatment of lung cancer. The selection of target patients at appropriate stages, breaking down of tumor immunosuppression as well as the objective measurement of tumor response to the therapy are major challenges for the development of immunotherapies for lung cancer. The clarifying of the mechanism of immune escape led to the above drug development, and immune-senescence has already become the hotspot in this field. 中国肺癌杂志编辑部 2012-10-20 /pmc/articles/PMC5999828/ /pubmed/23075686 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.10.08 Text en 版权所有©《中国肺癌杂志》编辑部2012 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | 综述 肺癌的免疫治疗临床研究进展 |
title | 肺癌的免疫治疗临床研究进展 |
title_full | 肺癌的免疫治疗临床研究进展 |
title_fullStr | 肺癌的免疫治疗临床研究进展 |
title_full_unstemmed | 肺癌的免疫治疗临床研究进展 |
title_short | 肺癌的免疫治疗临床研究进展 |
title_sort | 肺癌的免疫治疗临床研究进展 |
topic | 综述 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999828/ https://www.ncbi.nlm.nih.gov/pubmed/23075686 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.10.08 |
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