Regorafenib is suitable for advanced colorectal cancer patients who have previously received trifluridine/tipiracil plus bevacizumab

被引:2
作者
Matsumoto, Toshihiko [1 ,4 ]
Ikoma, Tatsuki [1 ]
Yamamura, Shogo [1 ]
Miura, Kou [2 ]
Tsuduki, Takao [2 ]
Watanabe, Takanori [3 ]
Nagai, Hiroki [1 ]
Takatani, Masahiro [2 ]
Yasui, Hisateru [1 ]
机构
[1] Kobe City Med Ctr Gen Hosp, Dept Clin Oncol, 2-1-1, Minatojima Minamimachi,Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Himeji Red Cross Hosp, Dept Internal Med, Himeji 1-12-1, Himeji, Hyogo 6708540, Japan
[3] Himeji Red Cross Hosp, Dept Surg, Himeji 1-12-1, Himeji, Hyogo 6708540, Japan
[4] Kansai Med Univ, Canc Treatment Ctr, 2-3-1 Hirakatashinmachi, Hirakata, Osaka 5731191, Japan
关键词
OPEN-LABEL; 1ST-LINE TREATMENT; ASIAN PATIENTS; DOUBLE-BLIND; PHASE-III; TAS-102; MULTICENTER; SURVIVAL; FOLFIRI; MONOTHERAPY;
D O I
10.1038/s41598-023-29706-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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