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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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.
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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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