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Hyperprogression under immunotherapy: a new form of immunotherapy response?—a narrative literature review
OBJECTIVE: Update the last known review, and summarize the definitions, diagnostic criteria, reported risk factors, possible mechanisms and potential biomarkers of hyperprogressive disease (HPD) under immunotherapy. BACKGROUND: Immunotherapy is a relatively new systemic therapy adding a new method o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350090/ https://www.ncbi.nlm.nih.gov/pubmed/34430364 http://dx.doi.org/10.21037/tlcr-21-575 |
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author | Lin, Miaozhen Vanneste, Ben G. L. Yu, Qiwen Chen, Zebin Peng, Jiayu Cai, Xiuyu |
author_facet | Lin, Miaozhen Vanneste, Ben G. L. Yu, Qiwen Chen, Zebin Peng, Jiayu Cai, Xiuyu |
author_sort | Lin, Miaozhen |
collection | PubMed |
description | OBJECTIVE: Update the last known review, and summarize the definitions, diagnostic criteria, reported risk factors, possible mechanisms and potential biomarkers of hyperprogressive disease (HPD) under immunotherapy. BACKGROUND: Immunotherapy is a relatively new systemic therapy adding a new method of treatment of especially advanced cancer patients. In a variety of immunotherapies, however, an unexpected acceleration of tumor growth, known as HPD, is observed in approximately 30% of patients after immune checkpoint inhibitor (ICI) treatment. HPD has a deleterious survival effect on patients and represents an urgent issue for both clinicians and patients. Existing literature has reviewed and summarized the definition, diagnostic criteria, reported risk factors and possible mechanisms of hyperprogression. However, with the gradual deepening of the exploration of HPD, researchers have made significant breakthroughs in elucidating the mechanism and mechanism of HPD and exploring biomarkers. METHODS: The search was conducted on Google Scholar and PubMed in January and May of 2021. We searched among English papers with no limitation on the publication year. We have included retrospective studies, case reports and basic researches related to HPD in the collection, we also referred to some review articles on HPD in recent years. A qualitative-interpretive approach was used for data extraction. CONCLUSIONS: HPD is considered to be an acceleration of tumor growth after ICI treatment that is not only due to immune infiltration but also due to real disease progression, with an incidence of about 4–30% in all retrospective published studies to date. Currently, the most widely used criteria of HPD contain Response Evaluation Criteria in Solid Tumors (RECIST) and tumor growth rate (TGR) or tumor growth kinetics. The common risk factors and underlying mechanisms of HPD have not yet been fully elucidated. However, based on the poor prognosis of HPD, there have been many advances in the exploration of biomarkers in recent years, like the prediction of HPD, such as LDH levels of peripheral blood, liquid biopsy, and radiomics, etc. |
format | Online Article Text |
id | pubmed-8350090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-83500902021-08-23 Hyperprogression under immunotherapy: a new form of immunotherapy response?—a narrative literature review Lin, Miaozhen Vanneste, Ben G. L. Yu, Qiwen Chen, Zebin Peng, Jiayu Cai, Xiuyu Transl Lung Cancer Res Review Article OBJECTIVE: Update the last known review, and summarize the definitions, diagnostic criteria, reported risk factors, possible mechanisms and potential biomarkers of hyperprogressive disease (HPD) under immunotherapy. BACKGROUND: Immunotherapy is a relatively new systemic therapy adding a new method of treatment of especially advanced cancer patients. In a variety of immunotherapies, however, an unexpected acceleration of tumor growth, known as HPD, is observed in approximately 30% of patients after immune checkpoint inhibitor (ICI) treatment. HPD has a deleterious survival effect on patients and represents an urgent issue for both clinicians and patients. Existing literature has reviewed and summarized the definition, diagnostic criteria, reported risk factors and possible mechanisms of hyperprogression. However, with the gradual deepening of the exploration of HPD, researchers have made significant breakthroughs in elucidating the mechanism and mechanism of HPD and exploring biomarkers. METHODS: The search was conducted on Google Scholar and PubMed in January and May of 2021. We searched among English papers with no limitation on the publication year. We have included retrospective studies, case reports and basic researches related to HPD in the collection, we also referred to some review articles on HPD in recent years. A qualitative-interpretive approach was used for data extraction. CONCLUSIONS: HPD is considered to be an acceleration of tumor growth after ICI treatment that is not only due to immune infiltration but also due to real disease progression, with an incidence of about 4–30% in all retrospective published studies to date. Currently, the most widely used criteria of HPD contain Response Evaluation Criteria in Solid Tumors (RECIST) and tumor growth rate (TGR) or tumor growth kinetics. The common risk factors and underlying mechanisms of HPD have not yet been fully elucidated. However, based on the poor prognosis of HPD, there have been many advances in the exploration of biomarkers in recent years, like the prediction of HPD, such as LDH levels of peripheral blood, liquid biopsy, and radiomics, etc. AME Publishing Company 2021-07 /pmc/articles/PMC8350090/ /pubmed/34430364 http://dx.doi.org/10.21037/tlcr-21-575 Text en 2021 Translational Lung Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Review Article Lin, Miaozhen Vanneste, Ben G. L. Yu, Qiwen Chen, Zebin Peng, Jiayu Cai, Xiuyu Hyperprogression under immunotherapy: a new form of immunotherapy response?—a narrative literature review |
title | Hyperprogression under immunotherapy: a new form of immunotherapy response?—a narrative literature review |
title_full | Hyperprogression under immunotherapy: a new form of immunotherapy response?—a narrative literature review |
title_fullStr | Hyperprogression under immunotherapy: a new form of immunotherapy response?—a narrative literature review |
title_full_unstemmed | Hyperprogression under immunotherapy: a new form of immunotherapy response?—a narrative literature review |
title_short | Hyperprogression under immunotherapy: a new form of immunotherapy response?—a narrative literature review |
title_sort | hyperprogression under immunotherapy: a new form of immunotherapy response?—a narrative literature review |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350090/ https://www.ncbi.nlm.nih.gov/pubmed/34430364 http://dx.doi.org/10.21037/tlcr-21-575 |
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