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临床试验/NCT06202417
NCT06202417已完成不适用

Fruquintinib in Refractory Metastatic Colorectal Cancer: A Real-world Study

Fudan University1 个研究点 分布在 1 个国家目标入组 520 人开始时间: 2021年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
520
试验地点
1
主要终点
OS

研究概览

简要总结

Fruquintinib is an oral tyrosine kinase inhibitor (TKI), which improves progression-free survival (PFS) and overall survival (OS) in patients with refractory metastatic colorectal cancer (mCRC). Here, we explore the real-world treatment patterns of fruquintinib in the third- or late-line setting for mCRC in six centers in China.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • (1) histology-confirmed metastatic CRC (mCRC); (2) disease progression on standard therapy with at least two lines of chemotherapy, including fluorouracil, oxaliplatin, and irinotecan with or without biologics such as bevacizumab and cetuximab; (3) fruquintinib administered as salvage treatment; (4) available clinical data.

排除标准

  • (1) lack of follow-up data; (2) fruquintinib administration as second-line treatment; (3) fruquintinib administration stopped after less than two cycles.

研究组 & 干预措施

monotherapy group

patients received fruquintinib alone

干预措施: Fruquintinib (Drug)

combine group

patients administered fruquintinib in combination with chemotherapy or/and anti-PD1 antibodies

干预措施: Fruquintinib (Drug)

结局指标

主要结局

OS

时间窗: Three years

OS was defined as the time from fruquintinib administration to death

PFS

时间窗: Three years

PFS was calculated from the date of fruquintinib administration to the first observation of disease progression or death

DCR

时间窗: During the medication period

DCR was determined as the proportion of patients who achieved complete response, partial response or stable disease assessed at least 6 weeks after drug administration

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Xu jianmin

Director of Colorectal Surgery

Fudan University

研究点 (1)

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