Cargando…
Regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab
Regorafenib is a standard salvage line therapy used for advanced colorectal cancer (CRC). Recently, trifluridine/tipiracil (TFTD) plus bevacizumab also showed promising efficacy as a salvage line therapy for advanced CRC. However, the efficacy and safety of regorafenib for patients with advanced CRC...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9918455/ https://www.ncbi.nlm.nih.gov/pubmed/36765099 http://dx.doi.org/10.1038/s41598-023-29706-6 |
_version_ | 1784886612615757824 |
---|---|
author | Matsumoto, Toshihiko Ikoma, Tatsuki Yamamura, Shogo Miura, Kou Tsuduki, Takao Watanabe, Takanori Nagai, Hiroki Takatani, Masahiro Yasui, Hisateru |
author_facet | Matsumoto, Toshihiko Ikoma, Tatsuki Yamamura, Shogo Miura, Kou Tsuduki, Takao Watanabe, Takanori Nagai, Hiroki Takatani, Masahiro Yasui, Hisateru |
author_sort | Matsumoto, Toshihiko |
collection | PubMed |
description | Regorafenib is a standard salvage line therapy used for advanced colorectal cancer (CRC). Recently, trifluridine/tipiracil (TFTD) plus bevacizumab also showed promising efficacy as a salvage line therapy for advanced CRC. However, the efficacy and safety of regorafenib for patients with advanced CRC who have previously received TFTD plus bevacizumab is unclear. We retrospectively collected clinicopathologic data from patients with advanced CRC who received regorafenib after TFTD plus bevacizumab in multiple institutions between April 2017 and June 2020.Thirty-four advanced CRC patients who received regorafenib were analyzed. The median age was 66.5 (range 43–81 years), 11 patients were male, and all had an ECOG performance status(PS) of 0 or 1. Twenty-two patients had left-sided tumors, 18 patients had RAS mutants, and 1 patient had a BRAF V600E mutation. The response rate was 0%, and the disease control rate was 31%. The median progression-free survival was 70 days (95% CI: 56–91), and the overall survival was 233 days (95% CI: 188–324). Treatment was discontinued in 32 patients, and 28 (82%) discontinued treatment due to progressive disease. The major grade 3 and4 toxicities were proteinurea (29%), hypertension (26%), hand-foot syndrome(15%), and platelet decrease (6%). Regorafenib after TFTD plus bevacizumab showed efficacy similar to that of the previous study, and no new adverse events were observed. |
format | Online Article Text |
id | pubmed-9918455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99184552023-02-12 Regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab Matsumoto, Toshihiko Ikoma, Tatsuki Yamamura, Shogo Miura, Kou Tsuduki, Takao Watanabe, Takanori Nagai, Hiroki Takatani, Masahiro Yasui, Hisateru Sci Rep Article Regorafenib is a standard salvage line therapy used for advanced colorectal cancer (CRC). Recently, trifluridine/tipiracil (TFTD) plus bevacizumab also showed promising efficacy as a salvage line therapy for advanced CRC. However, the efficacy and safety of regorafenib for patients with advanced CRC who have previously received TFTD plus bevacizumab is unclear. We retrospectively collected clinicopathologic data from patients with advanced CRC who received regorafenib after TFTD plus bevacizumab in multiple institutions between April 2017 and June 2020.Thirty-four advanced CRC patients who received regorafenib were analyzed. The median age was 66.5 (range 43–81 years), 11 patients were male, and all had an ECOG performance status(PS) of 0 or 1. Twenty-two patients had left-sided tumors, 18 patients had RAS mutants, and 1 patient had a BRAF V600E mutation. The response rate was 0%, and the disease control rate was 31%. The median progression-free survival was 70 days (95% CI: 56–91), and the overall survival was 233 days (95% CI: 188–324). Treatment was discontinued in 32 patients, and 28 (82%) discontinued treatment due to progressive disease. The major grade 3 and4 toxicities were proteinurea (29%), hypertension (26%), hand-foot syndrome(15%), and platelet decrease (6%). Regorafenib after TFTD plus bevacizumab showed efficacy similar to that of the previous study, and no new adverse events were observed. Nature Publishing Group UK 2023-02-10 /pmc/articles/PMC9918455/ /pubmed/36765099 http://dx.doi.org/10.1038/s41598-023-29706-6 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Matsumoto, Toshihiko Ikoma, Tatsuki Yamamura, Shogo Miura, Kou Tsuduki, Takao Watanabe, Takanori Nagai, Hiroki Takatani, Masahiro Yasui, Hisateru Regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab |
title | Regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab |
title_full | Regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab |
title_fullStr | Regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab |
title_full_unstemmed | Regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab |
title_short | Regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab |
title_sort | regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9918455/ https://www.ncbi.nlm.nih.gov/pubmed/36765099 http://dx.doi.org/10.1038/s41598-023-29706-6 |
work_keys_str_mv | AT matsumototoshihiko regorafenibissuitableforadvancedcolorectalcancerpatientswhohavepreviouslyreceivedtrifluridinetipiracilplusbevacizumab AT ikomatatsuki regorafenibissuitableforadvancedcolorectalcancerpatientswhohavepreviouslyreceivedtrifluridinetipiracilplusbevacizumab AT yamamurashogo regorafenibissuitableforadvancedcolorectalcancerpatientswhohavepreviouslyreceivedtrifluridinetipiracilplusbevacizumab AT miurakou regorafenibissuitableforadvancedcolorectalcancerpatientswhohavepreviouslyreceivedtrifluridinetipiracilplusbevacizumab AT tsudukitakao regorafenibissuitableforadvancedcolorectalcancerpatientswhohavepreviouslyreceivedtrifluridinetipiracilplusbevacizumab AT watanabetakanori regorafenibissuitableforadvancedcolorectalcancerpatientswhohavepreviouslyreceivedtrifluridinetipiracilplusbevacizumab AT nagaihiroki regorafenibissuitableforadvancedcolorectalcancerpatientswhohavepreviouslyreceivedtrifluridinetipiracilplusbevacizumab AT takatanimasahiro regorafenibissuitableforadvancedcolorectalcancerpatientswhohavepreviouslyreceivedtrifluridinetipiracilplusbevacizumab AT yasuihisateru regorafenibissuitableforadvancedcolorectalcancerpatientswhohavepreviouslyreceivedtrifluridinetipiracilplusbevacizumab |