- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07790419
A Prospective, Single-Arm, Open-Label Clinical Study of the Efficacy and Safety of Hepatic Arterial Infusion Chemotherapy Combined With Targeted Therapy and a PD-1 Inhibitor in Patients With Postoperative Hepatocellular Carcinoma and Microvascular Invasion
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 4
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Wenlong Zhai, MD
- Número de teléfono: +86-371-66862231
- Correo electrónico: ven0371@126.com
Ubicaciones de estudio
-
-
Henan
-
Zhengzhou, Henan, Porcelana, 450052
- The First Affiliated Hospital of Zhengzhou University
-
Contacto:
- Wenlong Zhai, MD
- Número de teléfono: +86-371-66862231
- Correo electrónico: ven0371@126.com
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age 18-80 years, male or female;
- Pathologically confirmed hepatocellular carcinoma, with complete resection of all tumor nodules and negative surgical margins;
- Microvascular invasion (MVI) grade ≥ 1
- No other history of tumors and no preoperative anticancer treatment.
- ECOG: 0-1;
Baseline blood count tests and blood biochemistry must meet the following criteria:
Hemoglobin ≥80 g/L;
Absolute neutrophil count ≥1.5×109/L;
Platelet count ≥50×109/L;
Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤5 times the upper limit of normal (ULN);
Total bilirubin ≤3 times ULN;
Serum creatinine ≤1.5 times ULN;
Albumin ≥28 g/L; prothrombin time (PT) ≤19.5 s;
International normalized ratio (INR) ≤2.3
- Women of childbearing potential must agree to use contraception during the study and for 6 months after the study ends (e.g., intrauterine device, oral contraceptives, or condoms); serum or urine pregnancy test must be negative within 7 days before enrollment, and they must not be breastfeeding; men must agree to use contraception during the study and for 6 months after the study ends;
- Subjects voluntarily participate in this study, sign the informed consent form, are compliant, and cooperate with follow-up.
Exclusion Criteria:
1. Patients with any active autoimmune disease or a history of autoimmune disease (including, but not limited to: autoimmune hepatitis, interstitial pneumonia, uveitis, enteritis, hepatitis, hypophysitis, vasculitis, nephritis, hyperthyroidism; patients with vitiligo; patients whose childhood asthma has completely resolved and who require no intervention as adults may be included; asthma requiring bronchodilator intervention for medical management cannot be included);
2. Pregnancy or lactation;
3. Over 80 years old;
4. Prior systemic chemotherapy or radiotherapy;
5. Concomitant malignant pleural effusion or ascites;
6. History of organ transplantation (including autologous bone marrow transplantation and peripheral stem cell transplantation);
7. Concomitant infection requiring anti-infective treatment;
8. Concomitant peripheral nervous system disease or a history of significant psychiatric disease and central nervous system disease;
9. Diagnosis of other types of malignant tumors within 5 years, excluding non-melanoma skin cancer and carcinoma in situ of the cervix;
10. Uncorrectable coagulation disorders;
11. Significant ECG abnormalities or obvious clinical symptoms of heart disease, such as congestive heart failure (CHF), clinically significant coronary heart disease, difficult-to-control arrhythmias, and hypertension;
12. History of myocardial infarction within 12 months, or cardiac function class III or IV;
13. Severe liver disease (e.g., cirrhosis), kidney disease, respiratory disease, uncontrolled diabetes, or other systemic diseases;
14. Individuals deemed unsuitable for inclusion by the investigator.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: HAIC+Targeted Therapy +PD-1 Inhibitor
Hepatic arterial infusion chemotherapy (HAIC): to be performed within 4-8 weeks after liver cancer surgery, as follows: Oxaliplatin 65 mg/m², IA (intra-arterial), Day 1, 0-5 hours: 5-FU 1200 mg/m², IA, maintained for 23 hours. After catheter removal, a pressure dressing for hemostasis for 6-12 hours is sufficient before discharge. The above HAIC treatment will be repeated every 3-4 weeks for a total of 2 cycles. Targeted drugs: Including lenvatinib: oral administration according to body weight; body weight ≥60 kg, 8-12 mg QD; body weight <60 kg, 4-8 mg QD; donafenib: 80 mg BID; apatinib: 250 mg QD. The above targeted drugs will be appropriately adjusted according to the patient's tolerance to toxic side effects. PD-1 inhibitors : sintilimab 200 mg Q3W, ivgtt; camrelizumab 200 mg Q3W, ivgtt; tislelizumab 200 mg Q3W, ivgtt. This study will follow participants for disease recurrence and disease-free survival for at least 2 years. After all participants complete treatment or the |
Oxaliplatin and 5-Fluorouracil(5-FU)administeredvia hepatic artery infusion
Oraltargeted therapy administered daily
PD--1 inhibitor administered viaintravenous infusion
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Disease-free survival (DFS)
Periodo de tiempo: From the date of randomization until the date of first documented recurrence or death from any cause, whichever came first, assessed up to 28 months.
|
Disease-free survival (DFS) is defined as the time from the date of randomization to the first documented tumor recurrence, metastasis, or death from any cause, whichever occurs first.
|
From the date of randomization until the date of first documented recurrence or death from any cause, whichever came first, assessed up to 28 months.
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Overall survival (OS)
Periodo de tiempo: From the date of randomization until death from any cause, assessed up to 28 months.
|
Overall survival (OS) is defined as the time from randomization to death from any cause.
For subjects lost to follow-up before death, the time of last follow-up is generally used as the death time.
|
From the date of randomization until death from any cause, assessed up to 28 months.
|
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Safety endpoints
Periodo de tiempo: Through study completion, an average of 28 months.
|
Exposure to the investigational drug and the incidence, nature, and severity of adverse events (including serious adverse events) will be recorded.
|
Through study completion, an average of 28 months.
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2025-KY-2003-002
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .