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Clinical Trials in China / NCT06602011
Recruiting Observational

Triple Therapy for Intermediate-advanced HCC With BDTT (TALENP002)

NCT06602011 · tracked via the Priya Life Science China tracker
Sponsor
Fujian Provincial Hospital
Phase
Observational
Started
2024-09-30
Last updated
2024-10-15

Condition(s) studied

Hepatocellular Carcinoma

Investigational drug(s) / intervention(s)

TACE, Lenvatinib, combined with Tislelizumab group

TACE, Lenvatinib, combined with Tislelizumab group: TACE, Lenvatinib \[8mg(\<60kg)/12mg(\>60kg) orally daily\] combination with Tislelizumab (200mg administered intravenous injection on Day 1 of each 21-day cycle). After the triple therapy, surgical resection is an option if assessed by the investigator to be feasible, or continued until disease progression or intolerable if not.

Study summary

This is a multicenter, Single-arm, Real-world Study to evaluate the efficacy and safety of Transcatheter arterial chemoembolization (TACE), Lenvatinib combined with Tislelizumab (Triple Therapy) for patients with Hepatocellular Carcinoma (HCC) with bile duct tumor thrombus (BDTT).

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age between 18 and 75 years old; 2. Patients with clinical diagnosis of Hepatocellular Carcinoma (HCC) combined with bile duct tumor thrombus (BDTT) (refer to the diagnostic criteria of the Chinese Expert Consensus on Multidisciplinary Diagnosis and Treatment of HCC with BDTT (2020 Edition)), BCLC Stage B or Stage C, and unresectable HCC (decided after multidisciplinary discussion); 3. Patients who had not received any tumor-related targeted, immunotherapy, radiotherapy and chemotherapy before enrollment; 4. Patients with at least one measurable lesion according to the mRECIST criteria (measurable lesion with a CT/MRI scan length diameter ≥ 10 mm and measurable lesion has not received localized treatment such as TACE, radiofrequency, cryotherapy, etc.); 5. ECOG score: 0-1; 6. liver function Child-Pugh class A or B; if combined with obstructive jaundice, total bilirubin ≤50umol/L is required. If higher than 50umol/L, biliary drainage is recommended; 7. Blood routine: absolute neutrophil count ≥1.5×10\^9/L, Hb≥8.5g/L, PLT≥75×10\^9/L; 8. No history of severe cardiac arrhythmia or heart failure; no history of severe ventilatory dysfunction or severe pulmonary infection; no acute or chronic renal failure with creatinine clearance \>40mL/min; 9. Expected survival time greater than 3 months. Exclusion Criteria: 1. The tumor with extrahepatic metastasis or invaded adjacent organs; 2. Patients received other anti-tumor treatments; 3. Existence of contraindications to TACE; 4. History of allergy to the components or excipients of Lenvatinib or Tislelizumab; 5. The patient has any active autoimmune disease or has an autoimmune disease with expected relapse. Patients are on immunosuppressive or systemic hormone therapy for immunosuppression; 6. Patients with proteinuria suggestive of ≥ 1 + in routine urine will undergo a 24-hour urine protein test for patients with ≥ 1 g of 24-hour urine protein; 7. Patients with co-morbidities of other malignant tumors; 8. Patients with co-morbid psychiatric disorders; 9. Patients with pregnant or lactating women; 10. Patients with organ transplant patients; 11. Patients with hypothyroidism or hyperthyroidism.

Primary outcome measure(s)

Trial sites (6)

FacilityCityRegionStatus
First Affiliated Hospital of Fujian Medical University Fuzhou Fujian Not Yet Recruiting
Mengchao Hepatobiliary Hospital of Fujian Medical University Fuzhou Fujian Not Yet Recruiting
Fujian Provincial Hospital Fuzhou Fujian Recruiting
Zhongshan Hospital of Xiamen University Xiamen Fujian Not Yet Recruiting
First Affiliated Hospital of Xiamen University Xiamen Fujian Not Yet Recruiting
Zhangzhou Affiliated Hospital of Fujian Medical University Zhangzhou Fujian Not Yet Recruiting

More Fujian Provincial Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06602011 on ClinicalTrials.gov ↗ ← All trials in China