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Intrahepatic Cholangiocarcinoma: State of the Art of FGFR Inhibitors
OBJECTIVE: Intrahepatic cholangiocarcinoma (iCCA), the second most common type of primary liver tumor, has an increasing incidence in the past few decades. iCCA is highly malignant, with a 5-year survival rate of approximately 5-10%. Surgical resection is usually the prescribed treatment for patient...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482710/ https://www.ncbi.nlm.nih.gov/pubmed/33618536 http://dx.doi.org/10.1177/1073274821989314 |
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author | Wu, Tianyu Jiang, Xiaoqing Zhang, Xin Wu, Bodeng Xu, Bin Liu, Xiaoliu Zheng, Lei Wang, Yu |
author_facet | Wu, Tianyu Jiang, Xiaoqing Zhang, Xin Wu, Bodeng Xu, Bin Liu, Xiaoliu Zheng, Lei Wang, Yu |
author_sort | Wu, Tianyu |
collection | PubMed |
description | OBJECTIVE: Intrahepatic cholangiocarcinoma (iCCA), the second most common type of primary liver tumor, has an increasing incidence in the past few decades. iCCA is highly malignant, with a 5-year survival rate of approximately 5-10%. Surgical resection is usually the prescribed treatment for patients with early stage iCCA; however, patients are usually in an advanced stage iCCA upon diagnosis. Currently, targeted therapy combined with chemotherapy and other comprehensive treatment measures have been mainly adopted as palliative treatment measures. As a common candidate of targeted therapy, FGFR inhibitors have demonstrated their unique advantages in clinical trials. At present, the prospect of FGFR targeted therapy is encouraging. The landscape of FGFR inhibitors in iCCA is needed to be showed urgently. METHODS: We searched relative reports of clinical trials on FGFR inhibitors in PubMed as well as Web of Science. We also concluded other available clinical trials of FGFR inhibitors (Data were collected from clinicaltrials.gov). RESULTS: Several relatively effective targeted drugs are being used in clinical trials. Some preliminary results indicate the outlook of targeted therapy such as BGJ398, TAS120, and HSP90 inhibitors. CONCLUSIONS: In summary, FGFR targeted therapy has broad prospects for the treatment of iCCA. |
format | Online Article Text |
id | pubmed-8482710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-84827102021-10-01 Intrahepatic Cholangiocarcinoma: State of the Art of FGFR Inhibitors Wu, Tianyu Jiang, Xiaoqing Zhang, Xin Wu, Bodeng Xu, Bin Liu, Xiaoliu Zheng, Lei Wang, Yu Cancer Control Review OBJECTIVE: Intrahepatic cholangiocarcinoma (iCCA), the second most common type of primary liver tumor, has an increasing incidence in the past few decades. iCCA is highly malignant, with a 5-year survival rate of approximately 5-10%. Surgical resection is usually the prescribed treatment for patients with early stage iCCA; however, patients are usually in an advanced stage iCCA upon diagnosis. Currently, targeted therapy combined with chemotherapy and other comprehensive treatment measures have been mainly adopted as palliative treatment measures. As a common candidate of targeted therapy, FGFR inhibitors have demonstrated their unique advantages in clinical trials. At present, the prospect of FGFR targeted therapy is encouraging. The landscape of FGFR inhibitors in iCCA is needed to be showed urgently. METHODS: We searched relative reports of clinical trials on FGFR inhibitors in PubMed as well as Web of Science. We also concluded other available clinical trials of FGFR inhibitors (Data were collected from clinicaltrials.gov). RESULTS: Several relatively effective targeted drugs are being used in clinical trials. Some preliminary results indicate the outlook of targeted therapy such as BGJ398, TAS120, and HSP90 inhibitors. CONCLUSIONS: In summary, FGFR targeted therapy has broad prospects for the treatment of iCCA. SAGE Publications 2021-02-23 /pmc/articles/PMC8482710/ /pubmed/33618536 http://dx.doi.org/10.1177/1073274821989314 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Wu, Tianyu Jiang, Xiaoqing Zhang, Xin Wu, Bodeng Xu, Bin Liu, Xiaoliu Zheng, Lei Wang, Yu Intrahepatic Cholangiocarcinoma: State of the Art of FGFR Inhibitors |
title | Intrahepatic Cholangiocarcinoma: State of the Art of FGFR Inhibitors |
title_full | Intrahepatic Cholangiocarcinoma: State of the Art of FGFR Inhibitors |
title_fullStr | Intrahepatic Cholangiocarcinoma: State of the Art of FGFR Inhibitors |
title_full_unstemmed | Intrahepatic Cholangiocarcinoma: State of the Art of FGFR Inhibitors |
title_short | Intrahepatic Cholangiocarcinoma: State of the Art of FGFR Inhibitors |
title_sort | intrahepatic cholangiocarcinoma: state of the art of fgfr inhibitors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482710/ https://www.ncbi.nlm.nih.gov/pubmed/33618536 http://dx.doi.org/10.1177/1073274821989314 |
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