← Back to all trials
Not Yet Recruiting
NCT05697237
Carlizumab Plus Sovantinib in Second-line Treatment of Advanced or Metastatic Cholangiocarcinoma
Conditions: Cholangiocarcinoma
Sex: All
Ages: 18 Years – 75 Years
Phase: NA
Enrollment: 60
Sponsor: First Affiliated Hospital Xi'an Jiaotong University
Summary
The incidence of cholangiocarcinoma is high, the radical resection rate is low, the postoperative recurrence is easy, the prognosis is poor.Gemcitabine combined with cisplatin (GC) is the standard first-line treatment for patients with advanced biliary carcinoma, and up to now there is no standard second-line treatment Commend.Carrilizumab was highly effective in previous studies,Its combined GEMOX protocol has been published in the "Guidelines for the Diagnosis and Treatment of Gallbladder Cancer (2019 Edition)" and the "China Clinical Oncology" The Society's (CSCO) Guidelines for the Diagnosis and Treatment of Biliary alignancies 2020 is recommended for the first-line treatment of advanced biliary cancers.Solfantinib is targeted at VEGFR1, 2, 3, FGFR1And CSF1R highly selective small molecule targeted therapy drugs.
Data from a preliminary phase 2 clinical trial observed sofantinib therapy Survival benefits of cholangiocarcinoma patients in China.
Eligibility Criteria
Inclusion Criteria:Advanced inability to root was pathologically confirmed Patients with curatively resected or metastatic bile duct epithelial cell carcinoma;had previously received systemic antitumor therapy with a chemotherapy regimen (including gemcitabine)Age ≥18 and under 75Predicted survival ≥3 monthsECOG score 0-1Child-Pugh score < 8There was at least one measurable tumor lesion with a long diameter ≥10 mm and a short diameter ≥15 mm on spiral CT,For general CT or physical examination, the maximum diameter must be ≥20mmThe results of liver and kidney function and blood routine examination within 1 week before enrollment were consistent with the following conditions:ANC≥1.5×10^9/L,PLT≥80×10^9/L,HGB≥80g/L,Cr≤1.5×ULN,TBIL≤2.5×ULN,ALP≤2.5×ULN,AST≤2.5×ULN,ALT≤2.5×ULNPatients participate voluntarily and sign informed consent formsExclusion Criteria:Known allergies to carrilizumab or solfantinib machine componentsPatients with obstructive jaundice who could not reach the upper limit of TBIL≤2.5 times of normal value after surgical interventionPatients with biliary obstruction that may occur or worsen within 4 to 6 weeksPatients with obvious coagulation mechanism disorder, active bleeding and bleeding tendencyHistory of other malignancies within 5 years (fully treated basal cell carcinoma of the skin, cervical cancer in situ)Interstitial pneumonia or pulmonary fibrosisUncontrollable pleural effusion or ascitesSevere uncontrolled medical disease, acute infection, recent history of myocardial infarction (within 3 months)Pregnant or lactating mothers who refused to take appropriate contraceptive measures during the course of the study;The researchers determined that the patients were not suitable for this study
Source: ClinicalTrials.gov (NCT05697237). StuddyBuddy aggregates publicly available trial information.