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- Ensayo clínico NCT07745790
Safety and Efficacy of Multimodal Thermal Therapy (MTT) Combined With KRAS G12V mRNA Vaccine, S-1, and Sintilimab in Patients With Metastatic Pancreatic Cancer
30 de julio de 2026 actualizado por: Ruijin Hospital
A Study of Multimodal Thermal Therapy (MTT) Combined With KRAS G12V mRNA Vaccine, S-1, and Sintilimab for Safety and Efficacy in Patients With Metastatic Pancreatic Ductal Adenocarcinoma Who Have Disease Progression After or Are Intolerant to Standard First-Line Therapy
This is a single-arm, single-center, exploratory clinical study.
A total of 20 participants with metastatic pancreatic ductal adenocarcinoma (with liver or lung metastasis) who have experienced disease progression after or are intolerant to standard first-line chemotherapy (based on the AG regimen [Albumin-bound Paclitaxel plus Gemcitabine]) will be enrolled.The study aims to evaluate the safety, efficacy, and underlying immunological mechanisms of Multimodal Thermal Therapy (MTT) combined with a KRAS G12V mRNA vaccine, S-1, and Sintilimab.
Descripción general del estudio
Estado
Aún no reclutando
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Estimado)
20
Fase
- Fase 2
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: baiyong shen
- Número de teléfono: +86 18817821319
- Correo electrónico: shenby@shsmu.edu.cn
Ubicaciones de estudio
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Porcelana, 200000
- Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
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Contacto:
- baiyong shen
- Número de teléfono: +86 18817821319
- Correo electrónico: shenby@shsmu.edu.cn
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- Aged ≥ 18 years old with no restriction on gender.
- Patients with advanced pancreatic cancer or postoperative recurrent pancreatic cancer confirmed by histopathological or cytological examination.
- Tumor tissues are confirmed to carry KRAS G12V mutation via sequencing and bioinformatics analysis (valid test reports obtained within the previous 12 months and recognized by the investigator are acceptable). In the dose expansion phase, patients must harbor at least one HLA allele capable of effectively presenting the corresponding antigen, including HLA-A11:01, HLA-A03:01, HLA-A30:01, HLA-A68:01, HLA-C01:02, HLA-C03:03, and HLA-C03:04.
- Disease resistance or intolerance to prior AG-based chemotherapy regimens.
- Presence of liver metastasis or lung metastasis.
- Eastern Cooperative Oncology Group Performance Status (ECOG PS) score of 0 or 1.
- Child-Pugh score ≤ 7 points.
- Expected overall survival of at least 3 months.
Exclusion Criteria:
- Presence of diffuse hepatic or pulmonary metastases.
- Prior local treatment including radiofrequency ablation, microwave ablation, radiotherapy or other local therapies for metastatic lesions.
- Current participation in other interventional clinical studies and receiving investigational treatment.
- Diagnosis of any other malignant disease within 5 years prior to the first study drug administration (excluding radically treated basal cell carcinoma, squamous cell carcinoma of the skin, and/or radically resected in situ carcinoma).
- Prior history of solid organ or hematopoietic stem cell transplantation.
- Any disease requiring systemic treatment with corticosteroids (prednisone or equivalent daily dose > 10 mg) or other immunosuppressive agents within 14 days prior to enrollment.
- Previous or current diagnosis of brain metastases with incompletely controlled symptoms (i.e., persistent or aggravated symptoms, or requirement for adjusted symptomatic treatment to maintain symptom relief).
- Presence of uncontrolled active infection.
- Renal dysfunction defined as serum creatinine > 176.8 μmol/L or creatinine clearance < 30 mL/min.
- Uncorrectable coagulation abnormalities, including platelet count < 50×10⁹/L, prothrombin time > 18 seconds, or prothrombin activity < 40%, which cannot be corrected.
- History of esophagogastric variceal rupture without effective treatment via endoscopy, interventional therapy or surgery.
- Patients with psychiatric disorders in the acute episode stage.
- Women of childbearing potential who are pregnant, breastfeeding, or planning to become pregnant during the study treatment period or within 3 months after the end of study treatment.
- Prior systemic pharmacotherapy, radiotherapy or local hepatic treatment with an interval of < 1 month from the last systemic or local hepatic treatment to the first study drug administration.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿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 |
|---|---|
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Experimental: Treatment Group
MTT + KRAS G12V mRNA Vaccine + Sintilimab ± S-1 Participants will receive Multimodal Thermal Therapy (MTT) combined with KRAS G12V mRNA vaccine and sintilimab. In addition, oral S-1 (tegafur/gimeracil/oteracil) will be administered to participants aged <80 years. Participants aged ≥80 years will receive MTT + KRAS G12V mRNA vaccine + sintilimab without S-1. |
The MTT system is a medical device that performs sequential ablation therapy.
Treatment consists of initial cryoablation followed immediately by radiofrequency ablation (RFA) to achieve a synergistic thermal effect against the tumor.
Administered via intramuscular injection at a dose of 1 mg.
The first dose will be given 1 to 3 days after Multimodal Thermal Therapy (MTT).
Subsequent doses will be administered every 3 weeks (Q3W) according to the study dosing schedule and clinical discretion.
Administered via intravenous infusion at a dose of 200 mg on Day 1 (d1).
Treatment will begin on 7 days after MTT and will be repeated every 3 weeks (Q3W) until disease progression or unacceptable toxicity.
Only participants aged <80 years will receive oral S-1.
Treatment starts on Day 7 after MTT at a dose of 40-60 mg twice daily (bid) on Days 1 to 14 (d1-14) of each cycle.
Cycles are repeated every 3 weeks (Q3W) until disease progression or unacceptable toxicity.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Incidence and Severity of Adverse Events (CTCAE v6.0)
Periodo de tiempo: From the start of treatment up to 90 days after the last dose (or end of treatment).
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To assess the safety profile of the combination regimen (MTT + KRAS G12V mRNA vaccine + Sintilimab ± S-1) in patients with metastatic pancreatic cancer.
Safety will be evaluated by recording the incidence, type, and maximum grade of adverse events (AEs) and serious adverse events (SAEs) according to the Common Terminology Criteria for Adverse Events (CTCAE) version 6.0.
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From the start of treatment up to 90 days after the last dose (or end of treatment).
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Frequency of Dose Modifications and Treatment Discontinuations
Periodo de tiempo: From the start of treatment up to 90 days after the last dose (or end of treatment).
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To evaluate patient tolerability to the multimodal regimen.
Tolerability is defined as the ability of participants to receive the full planned treatment.
Specifically, it measures the proportion of participants requiring dose modifications, treatment delays, treatment interruptions, or permanent discontinuation of any component of the therapy (MTT, S-1 [for those <80 years], Sintilimab, or mRNA vaccine) due to adverse events.
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From the start of treatment up to 90 days after the last dose (or end of treatment).
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Progression-Free Survival (RECIST 1.1)
Periodo de tiempo: From the date of first study intervention until disease progression, death, or the last effective follow-up (up to approximately 24 months)
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Time from the date of first study intervention to the date of radiographic disease progression per RECIST version 1.1, death from any cause, or the date of the last effective follow-up.
Radiographic assessments will be performed every 1-2 months using contrast-enhanced abdominal MRI or CT imaging.
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From the date of first study intervention until disease progression, death, or the last effective follow-up (up to approximately 24 months)
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Overall Survival
Periodo de tiempo: up to approximately 36 months
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Time from the date of first study intervention to the date of death from any cause or the date of the last confirmed survival follow-up.
Long-term survival will be tracked through regular follow-up visits until death, loss to follow-up, or study termination.
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up to approximately 36 months
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Estimado)
13 de julio de 2026
Finalización primaria (Estimado)
31 de julio de 2029
Finalización del estudio (Estimado)
31 de julio de 2029
Fechas de registro del estudio
Enviado por primera vez
1 de julio de 2026
Primero enviado que cumplió con los criterios de control de calidad
30 de julio de 2026
Publicado por primera vez (Actual)
4 de agosto de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
4 de agosto de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
30 de julio de 2026
Última verificación
1 de junio de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades del sistema endocrino
- Neoplasias por sitio
- Neoplasias
- Enfermedades de las vías respiratorias
- Neoplasias del Sistema Digestivo
- Enfermedades del Sistema Digestivo
- Enfermedades pulmonares
- Neoplasias de glándulas endocrinas
- Enfermedades pancreáticas
- Enfermedades del HIGADO
- Neoplasias de las vías respiratorias
- Neoplasias torácicas
- Neoplasias Pulmonares
- Neoplasias pancreáticas
- Neoplasias Hepaticas
- Terapéutica
- Terapia con drogas
- Sistemas de administración de medicamentos
- sintilimab
- S 1 (combinación)
Otros números de identificación del estudio
- PLP1-13114
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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