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Regorafenib in Refractory Metastatic Colorectal Cancer: A Multi-Center Retrospective Study
BACKGROUND: Regorafenib improves progression-free survival (PFS) and overall survival (OS) in patients with refractory metastatic colorectal cancer (mCRC). Here, we report the treatment patterns of regorafenib in the third- or late-line setting for mCRC in four centers in China. PATIENTS AND METHODS...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007238/ https://www.ncbi.nlm.nih.gov/pubmed/35433423 http://dx.doi.org/10.3389/fonc.2022.838870 |
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author | Xu, Donghao Liu, Yu Tang, Wentao Xu, Lingsha Liu, Tianyu Jiang, Yudong Zhou, Shizhao Qin, Xiaorui Li, Jisheng Zhao, Jiemin Ye, Lechi Chang, Wenju Xu, Jianmin |
author_facet | Xu, Donghao Liu, Yu Tang, Wentao Xu, Lingsha Liu, Tianyu Jiang, Yudong Zhou, Shizhao Qin, Xiaorui Li, Jisheng Zhao, Jiemin Ye, Lechi Chang, Wenju Xu, Jianmin |
author_sort | Xu, Donghao |
collection | PubMed |
description | BACKGROUND: Regorafenib improves progression-free survival (PFS) and overall survival (OS) in patients with refractory metastatic colorectal cancer (mCRC). Here, we report the treatment patterns of regorafenib in the third- or late-line setting for mCRC in four centers in China. PATIENTS AND METHODS: Patients with refractory mCRC in four centers in China administered regorafenib from February 1, 2018 to June 31, 2021 were enrolled. Patients were grouped into 3 cohorts, namely, the monotherapy (regorafenib alone), chemo (regorafenib plus chemotherapy), and immune [regorafenib plus anti-PD1 (programmed cell death 1) antibodies] groups. Demographic, clinical, survival and safety data were retrospectively analyzed. RESULTS: A total of 177 patients were included in this study. Of them, 116 (65.5%) were treated with regorafenib alone, while 28 (15.9%) and 33 (18.6%) were administered regorafenib plus chemotherapy and anti-PD1 antibodies, respectively. The median followed-up time was 9.2 months. The disease control rate (DCR) was 40.7%. The median PFS (mPFS) was 2.43 months and the median OS (mOS) was 12.2 months. The immune group had longer median PFS (3.5 m vs. 2.2 m, p = 0.043) compared with the monotherapy group. Patients administered regorafenib plus chemotherapy had longer median OS (15.9 m vs. 8.4 m, p = 0.032) compared with the monotherapy group. Patients who began regorafenib treatment at 120 mg had longer median PFS and OS compared with those who began at 80 mg (PFS: 3.7 m vs. 2.0 m; p <0.001; OS: 13.4 m vs. 10.2 m; p = 0.005). Patients with a final dose of 120 mg had longer median PFS and OS compared with the 80 mg or less group (PFS: 5.0 m vs. 2.3 m; p = 0.045; OS: UR (unreach) vs. 10.9 m; p = 0.003). There were 87.0% (154/177) patients who experienced AEs. Three groups had similar rates of AEs (86.2% vs. 89.3% vs. 87.9%; p = 0.89). CONCLUSION: Patients administered regorafenib alone or regorafenib in combination with other agents were relieved to some extent, with a disease control rate of 40.7%. Regorafenib plus anti-PD1 antibodies showed better PFS, while regorafenib plus chemotherapy had the most benefit in OS. There was no significant difference among three groups in terms of AEs. |
format | Online Article Text |
id | pubmed-9007238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90072382022-04-14 Regorafenib in Refractory Metastatic Colorectal Cancer: A Multi-Center Retrospective Study Xu, Donghao Liu, Yu Tang, Wentao Xu, Lingsha Liu, Tianyu Jiang, Yudong Zhou, Shizhao Qin, Xiaorui Li, Jisheng Zhao, Jiemin Ye, Lechi Chang, Wenju Xu, Jianmin Front Oncol Oncology BACKGROUND: Regorafenib improves progression-free survival (PFS) and overall survival (OS) in patients with refractory metastatic colorectal cancer (mCRC). Here, we report the treatment patterns of regorafenib in the third- or late-line setting for mCRC in four centers in China. PATIENTS AND METHODS: Patients with refractory mCRC in four centers in China administered regorafenib from February 1, 2018 to June 31, 2021 were enrolled. Patients were grouped into 3 cohorts, namely, the monotherapy (regorafenib alone), chemo (regorafenib plus chemotherapy), and immune [regorafenib plus anti-PD1 (programmed cell death 1) antibodies] groups. Demographic, clinical, survival and safety data were retrospectively analyzed. RESULTS: A total of 177 patients were included in this study. Of them, 116 (65.5%) were treated with regorafenib alone, while 28 (15.9%) and 33 (18.6%) were administered regorafenib plus chemotherapy and anti-PD1 antibodies, respectively. The median followed-up time was 9.2 months. The disease control rate (DCR) was 40.7%. The median PFS (mPFS) was 2.43 months and the median OS (mOS) was 12.2 months. The immune group had longer median PFS (3.5 m vs. 2.2 m, p = 0.043) compared with the monotherapy group. Patients administered regorafenib plus chemotherapy had longer median OS (15.9 m vs. 8.4 m, p = 0.032) compared with the monotherapy group. Patients who began regorafenib treatment at 120 mg had longer median PFS and OS compared with those who began at 80 mg (PFS: 3.7 m vs. 2.0 m; p <0.001; OS: 13.4 m vs. 10.2 m; p = 0.005). Patients with a final dose of 120 mg had longer median PFS and OS compared with the 80 mg or less group (PFS: 5.0 m vs. 2.3 m; p = 0.045; OS: UR (unreach) vs. 10.9 m; p = 0.003). There were 87.0% (154/177) patients who experienced AEs. Three groups had similar rates of AEs (86.2% vs. 89.3% vs. 87.9%; p = 0.89). CONCLUSION: Patients administered regorafenib alone or regorafenib in combination with other agents were relieved to some extent, with a disease control rate of 40.7%. Regorafenib plus anti-PD1 antibodies showed better PFS, while regorafenib plus chemotherapy had the most benefit in OS. There was no significant difference among three groups in terms of AEs. Frontiers Media S.A. 2022-03-30 /pmc/articles/PMC9007238/ /pubmed/35433423 http://dx.doi.org/10.3389/fonc.2022.838870 Text en Copyright © 2022 Xu, Liu, Tang, Xu, Liu, Jiang, Zhou, Qin, Li, Zhao, Ye, Chang and Xu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Xu, Donghao Liu, Yu Tang, Wentao Xu, Lingsha Liu, Tianyu Jiang, Yudong Zhou, Shizhao Qin, Xiaorui Li, Jisheng Zhao, Jiemin Ye, Lechi Chang, Wenju Xu, Jianmin Regorafenib in Refractory Metastatic Colorectal Cancer: A Multi-Center Retrospective Study |
title | Regorafenib in Refractory Metastatic Colorectal Cancer: A Multi-Center Retrospective Study |
title_full | Regorafenib in Refractory Metastatic Colorectal Cancer: A Multi-Center Retrospective Study |
title_fullStr | Regorafenib in Refractory Metastatic Colorectal Cancer: A Multi-Center Retrospective Study |
title_full_unstemmed | Regorafenib in Refractory Metastatic Colorectal Cancer: A Multi-Center Retrospective Study |
title_short | Regorafenib in Refractory Metastatic Colorectal Cancer: A Multi-Center Retrospective Study |
title_sort | regorafenib in refractory metastatic colorectal cancer: a multi-center retrospective study |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007238/ https://www.ncbi.nlm.nih.gov/pubmed/35433423 http://dx.doi.org/10.3389/fonc.2022.838870 |
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