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The global landscape of neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical trials
The neoadjuvant and adjuvant anti-PD-1/PD-L1 treatment has been increasingly noticed. To summarize the global landscape of these clinical trials will provide essential data for all the stakeholders of drug development. Based on the Trialtrove database, a total of 668 clinical trials initiated by the...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822713/ https://www.ncbi.nlm.nih.gov/pubmed/35135567 http://dx.doi.org/10.1186/s13045-022-01227-1 |
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author | Wu, Dawei Huang, Huiyao Zhang, Minghui Li, Ziwei Wang, Shuhang Yu, Yue Fang, Yuan Jiang, Ning Miao, Huilei Ma, Peiwen Tang, Yu Li, Ning |
author_facet | Wu, Dawei Huang, Huiyao Zhang, Minghui Li, Ziwei Wang, Shuhang Yu, Yue Fang, Yuan Jiang, Ning Miao, Huilei Ma, Peiwen Tang, Yu Li, Ning |
author_sort | Wu, Dawei |
collection | PubMed |
description | The neoadjuvant and adjuvant anti-PD-1/PD-L1 treatment has been increasingly noticed. To summarize the global landscape of these clinical trials will provide essential data for all the stakeholders of drug development. Based on the Trialtrove database, a total of 668 clinical trials initiated by the end of 2020 were retrospectively analyzed. We found that a rising capability of global neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical development has been achieved. High prevalent cancer types were extensively studied though the priorities in China and the United States were different. However, a lack of phase III trials and industry-sponsored trials was addressed. The confirmatory neoadjuvant trials were particularly insufficient, and the combination strategy mainly focused on chemotherapy. Thus, more public funding and accelerated regulatory strategies are needed in this field. Efforts should be made to confirm the benefit of neoadjuvant treatment and explore novel combination strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-022-01227-1. |
format | Online Article Text |
id | pubmed-8822713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88227132022-02-08 The global landscape of neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical trials Wu, Dawei Huang, Huiyao Zhang, Minghui Li, Ziwei Wang, Shuhang Yu, Yue Fang, Yuan Jiang, Ning Miao, Huilei Ma, Peiwen Tang, Yu Li, Ning J Hematol Oncol Letter to the Editor The neoadjuvant and adjuvant anti-PD-1/PD-L1 treatment has been increasingly noticed. To summarize the global landscape of these clinical trials will provide essential data for all the stakeholders of drug development. Based on the Trialtrove database, a total of 668 clinical trials initiated by the end of 2020 were retrospectively analyzed. We found that a rising capability of global neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical development has been achieved. High prevalent cancer types were extensively studied though the priorities in China and the United States were different. However, a lack of phase III trials and industry-sponsored trials was addressed. The confirmatory neoadjuvant trials were particularly insufficient, and the combination strategy mainly focused on chemotherapy. Thus, more public funding and accelerated regulatory strategies are needed in this field. Efforts should be made to confirm the benefit of neoadjuvant treatment and explore novel combination strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-022-01227-1. BioMed Central 2022-02-08 /pmc/articles/PMC8822713/ /pubmed/35135567 http://dx.doi.org/10.1186/s13045-022-01227-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Letter to the Editor Wu, Dawei Huang, Huiyao Zhang, Minghui Li, Ziwei Wang, Shuhang Yu, Yue Fang, Yuan Jiang, Ning Miao, Huilei Ma, Peiwen Tang, Yu Li, Ning The global landscape of neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical trials |
title | The global landscape of neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical trials |
title_full | The global landscape of neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical trials |
title_fullStr | The global landscape of neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical trials |
title_full_unstemmed | The global landscape of neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical trials |
title_short | The global landscape of neoadjuvant and adjuvant anti-PD-1/PD-L1 clinical trials |
title_sort | global landscape of neoadjuvant and adjuvant anti-pd-1/pd-l1 clinical trials |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822713/ https://www.ncbi.nlm.nih.gov/pubmed/35135567 http://dx.doi.org/10.1186/s13045-022-01227-1 |
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