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The Real-World Practice of Fruquintinib for Chinese Patients with Metastatic Colorectal Cancer
BACKGROUND: In FRESCO trial, a phase III study of fruquintinib demonstrated a significant improvement on the overall survival (OS) of patients with metastatic colorectal cancer (mCRC) who failed to response to available standard treatments. The aim of the current study was to evaluate the safety and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357312/ https://www.ncbi.nlm.nih.gov/pubmed/34393513 http://dx.doi.org/10.2147/CMAR.S313275 |
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author | Song, Yan Qu, Tao Zhang, Honggang Sun, Yongkun Cui, Chengxu Chi, Yihebali Zhang, Wen Wang, Xingyuan Yang, Lin |
author_facet | Song, Yan Qu, Tao Zhang, Honggang Sun, Yongkun Cui, Chengxu Chi, Yihebali Zhang, Wen Wang, Xingyuan Yang, Lin |
author_sort | Song, Yan |
collection | PubMed |
description | BACKGROUND: In FRESCO trial, a phase III study of fruquintinib demonstrated a significant improvement on the overall survival (OS) of patients with metastatic colorectal cancer (mCRC) who failed to response to available standard treatments. The aim of the current study was to evaluate the safety and effectiveness of fruquintinib in Chinese mCRC patients in the real-world setting. METHODS: Patients with mCRC treated with fruquintinib at our hospital were retrospectively reviewed. Patient demographics, treatment, adverse events and survival data were collected. OS and progression-free survival (PFS) were estimated using the Kaplan–Meier method. RESULTS: In total, 76 patients were evaluated from December 2018 to January 2020. The median (range) age was 59.5 (34–86) years, ECOG PS 0-1/2 was 86.8%/13.2%, and 38 (50%)/30 (39.5%) patients had experienced more than two prior therapies for mCRC. The median treatment duration was 3.6 cycles. Treatment-related adverse events (TRAEs) resulted in dose reduction were 17.1% of the patients without any treatment discontinuation. The most common grade 3 or 4 TRAEs were hypertension (9.2%), hand-foot skin reaction (7.9%), thrombocytopenia (3.9%), anaemia (2.6%), increased ALT (1.3%), oral mucositis (1.3%), proteinuria (1.3%) and neutropenia (1.3%). The median PFS was 5.1 months (95% CI 3.8–6.4 months), and the median OS was 12.0 months (95% CI 8.0–16.1 months). In patients with hypertension or hypothyroidism, a survival extension approximate to 6 months was observed, but the difference is not yet statistically significant. CEA decreased after fruquintinib treatment could be considered as a potential predictor for better OS. CONCLUSION: The outcome of this real-life study was consistent with that of the randomised controlled trial. There were no new safety concerns. Future studies of fruquintinib should be conducted to identify patients who tend to obtain more benefits from fruquintinib alone or in combination with other agents. |
format | Online Article Text |
id | pubmed-8357312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-83573122021-08-12 The Real-World Practice of Fruquintinib for Chinese Patients with Metastatic Colorectal Cancer Song, Yan Qu, Tao Zhang, Honggang Sun, Yongkun Cui, Chengxu Chi, Yihebali Zhang, Wen Wang, Xingyuan Yang, Lin Cancer Manag Res Original Research BACKGROUND: In FRESCO trial, a phase III study of fruquintinib demonstrated a significant improvement on the overall survival (OS) of patients with metastatic colorectal cancer (mCRC) who failed to response to available standard treatments. The aim of the current study was to evaluate the safety and effectiveness of fruquintinib in Chinese mCRC patients in the real-world setting. METHODS: Patients with mCRC treated with fruquintinib at our hospital were retrospectively reviewed. Patient demographics, treatment, adverse events and survival data were collected. OS and progression-free survival (PFS) were estimated using the Kaplan–Meier method. RESULTS: In total, 76 patients were evaluated from December 2018 to January 2020. The median (range) age was 59.5 (34–86) years, ECOG PS 0-1/2 was 86.8%/13.2%, and 38 (50%)/30 (39.5%) patients had experienced more than two prior therapies for mCRC. The median treatment duration was 3.6 cycles. Treatment-related adverse events (TRAEs) resulted in dose reduction were 17.1% of the patients without any treatment discontinuation. The most common grade 3 or 4 TRAEs were hypertension (9.2%), hand-foot skin reaction (7.9%), thrombocytopenia (3.9%), anaemia (2.6%), increased ALT (1.3%), oral mucositis (1.3%), proteinuria (1.3%) and neutropenia (1.3%). The median PFS was 5.1 months (95% CI 3.8–6.4 months), and the median OS was 12.0 months (95% CI 8.0–16.1 months). In patients with hypertension or hypothyroidism, a survival extension approximate to 6 months was observed, but the difference is not yet statistically significant. CEA decreased after fruquintinib treatment could be considered as a potential predictor for better OS. CONCLUSION: The outcome of this real-life study was consistent with that of the randomised controlled trial. There were no new safety concerns. Future studies of fruquintinib should be conducted to identify patients who tend to obtain more benefits from fruquintinib alone or in combination with other agents. Dove 2021-08-07 /pmc/articles/PMC8357312/ /pubmed/34393513 http://dx.doi.org/10.2147/CMAR.S313275 Text en © 2021 Song et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Song, Yan Qu, Tao Zhang, Honggang Sun, Yongkun Cui, Chengxu Chi, Yihebali Zhang, Wen Wang, Xingyuan Yang, Lin The Real-World Practice of Fruquintinib for Chinese Patients with Metastatic Colorectal Cancer |
title | The Real-World Practice of Fruquintinib for Chinese Patients with Metastatic Colorectal Cancer |
title_full | The Real-World Practice of Fruquintinib for Chinese Patients with Metastatic Colorectal Cancer |
title_fullStr | The Real-World Practice of Fruquintinib for Chinese Patients with Metastatic Colorectal Cancer |
title_full_unstemmed | The Real-World Practice of Fruquintinib for Chinese Patients with Metastatic Colorectal Cancer |
title_short | The Real-World Practice of Fruquintinib for Chinese Patients with Metastatic Colorectal Cancer |
title_sort | real-world practice of fruquintinib for chinese patients with metastatic colorectal cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357312/ https://www.ncbi.nlm.nih.gov/pubmed/34393513 http://dx.doi.org/10.2147/CMAR.S313275 |
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