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Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study

No definitive treatment strategy has been established for patients with metastatic colorectal cancer (mCRC) who experienced progression after three or more lines of chemotherapy. A total of 36 mCRC patients were enrolled in this retrospective study who received apatinib therapy under non-clinical tr...

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Autores principales: Gou, Miaomiao, Si, Haiyan, Zhang, Yong, Qian, Niansong, Wang, Zhikuan, Shi, Weiwei, Dai, Guanghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854587/
https://www.ncbi.nlm.nih.gov/pubmed/29545575
http://dx.doi.org/10.1038/s41598-018-22302-z
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author Gou, Miaomiao
Si, Haiyan
Zhang, Yong
Qian, Niansong
Wang, Zhikuan
Shi, Weiwei
Dai, Guanghai
author_facet Gou, Miaomiao
Si, Haiyan
Zhang, Yong
Qian, Niansong
Wang, Zhikuan
Shi, Weiwei
Dai, Guanghai
author_sort Gou, Miaomiao
collection PubMed
description No definitive treatment strategy has been established for patients with metastatic colorectal cancer (mCRC) who experienced progression after three or more lines of chemotherapy. A total of 36 mCRC patients were enrolled in this retrospective study who received apatinib therapy under non-clinical trial setting after progression in People’s liberation army general Hospital from March 2015 and August 2017. Progression free survival (PFS), overall survival (OS), disease control rate (DCR), objective response rate (ORR) and treatment-related adverse events (AEs) were reviewed and evaluated. Five patients achieved partial response (PR), and 25 achieved stable disease (SD), and 6 achieved progression disease (PD), illustrating a DCR of 83.3% and an ORR of 13.9%. Median PFS was 3.82 m and median OS was not reached. The toxicities associated with apatinib were generally acceptable with a total grade 3/4 adverse event incidence of 27.8%. The most common grade 3/4 adverse events were hypertension (n = 4, 11.1%), liver function damage (n = 3, 8.3%) and hand–foot syndrome (n = 2, 5.6%). No drug-related death occurred. Apatinib therapy provides a reasonable option with an acceptable safety profile for Chinese mCRC patients failed to prior chemotherapy.
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spelling pubmed-58545872018-03-22 Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study Gou, Miaomiao Si, Haiyan Zhang, Yong Qian, Niansong Wang, Zhikuan Shi, Weiwei Dai, Guanghai Sci Rep Article No definitive treatment strategy has been established for patients with metastatic colorectal cancer (mCRC) who experienced progression after three or more lines of chemotherapy. A total of 36 mCRC patients were enrolled in this retrospective study who received apatinib therapy under non-clinical trial setting after progression in People’s liberation army general Hospital from March 2015 and August 2017. Progression free survival (PFS), overall survival (OS), disease control rate (DCR), objective response rate (ORR) and treatment-related adverse events (AEs) were reviewed and evaluated. Five patients achieved partial response (PR), and 25 achieved stable disease (SD), and 6 achieved progression disease (PD), illustrating a DCR of 83.3% and an ORR of 13.9%. Median PFS was 3.82 m and median OS was not reached. The toxicities associated with apatinib were generally acceptable with a total grade 3/4 adverse event incidence of 27.8%. The most common grade 3/4 adverse events were hypertension (n = 4, 11.1%), liver function damage (n = 3, 8.3%) and hand–foot syndrome (n = 2, 5.6%). No drug-related death occurred. Apatinib therapy provides a reasonable option with an acceptable safety profile for Chinese mCRC patients failed to prior chemotherapy. Nature Publishing Group UK 2018-03-15 /pmc/articles/PMC5854587/ /pubmed/29545575 http://dx.doi.org/10.1038/s41598-018-22302-z Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gou, Miaomiao
Si, Haiyan
Zhang, Yong
Qian, Niansong
Wang, Zhikuan
Shi, Weiwei
Dai, Guanghai
Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study
title Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study
title_full Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study
title_fullStr Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study
title_full_unstemmed Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study
title_short Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study
title_sort efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854587/
https://www.ncbi.nlm.nih.gov/pubmed/29545575
http://dx.doi.org/10.1038/s41598-018-22302-z
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