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临床试验/NCT06378580
NCT06378580已完成不适用

The Prognostic Impact of Surufatinib for the Treatment of Advanced Pancreatic Ductal Adenocarcinoma

Luo Cong1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2022年7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
发起方
入组人数
72
试验地点
1
主要终点
Median progression-free survival

研究概览

简要总结

Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive tumor with a poor prognosis, despite the emergence of chemotherapies, unmet medical needs and limited treatment options still exist for patients with metastatic PDAC (mPDAC). Surufatinib is a small-molecule tyrosine kinase inhibitor that targets vascular endothelial growth factor (VEGFR) 1, 2, 3, fibroblast growth factor receptor 1 (FGFR1), and colony stimulating factor 1 receptor (CSF-1R), and ex vivo experiments have demonstrated its effect on PC models.

A retrospective analysis of patients with PDAC who underwent surufatinib at Zhejiang Cancer Hospital (Hangzhou,China) from July 2022 to July 2023.The database was extracted from the preoperative demographics, blood markers, and surgical pathology information of patients undergoing surufatinib in the investigators' hospital.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • (i) were over 18 years old; (ii) had a histological diagnosis of pancreatic adenocarcinoma; (iii) had at least one measurable lesion; (iv) had undergone at least two cycles of surufatinib treatment.

排除标准

  • (i)non-R0 resection; (ii) Combined with other malignant tumors.

研究组 & 干预措施

Surufatinib combine immune checkpoint inhibitor

干预措施: Surufatinib combine immune checkpoint inhibitor (Drug)

Chemotherapy

干预措施: AG/FOLFIRINOX (Drug)

结局指标

主要结局

Median progression-free survival

时间窗: 5 months

次要结局

未报告次要终点

研究者

发起方
Luo Cong
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Luo Cong

Director

Zhejiang Cancer Hospital

研究点 (1)

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