Immunotheray Combined With Simvastatin and Target Therapy and Chemotharepy for Advanced Colorectal Cancer
A Multicenter, Prospective, Phase II Exploratory Study on the First-line Treatment of MSS/ PMMR-type Advanced Colorectal Cancer With Adebrelimab Combined With Simvastatin and Targeted and Chemotherapy
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Yanhong Gu
- Número de teléfono: +86 25 6830 6714
- Correo electrónico: guyanhong@njmu.edu.cn
Ubicaciones de estudio
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Jiangsu
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Nanjing, Jiangsu, Porcelana, 210008
- Reclutamiento
- Jiangsu Province Hospital (the First Affiliated Hospital With Nanjing Medical University)
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Contacto:
- Yanhong Gu
- Número de teléfono: +86 25 6830 6714
- Correo electrónico: guyanhong@njmu.edu.cn
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Nanjing, Jiangsu, Porcelana
- Aún no reclutando
- Nanjing First Hospital, Nanjing Medical University Affiliated Hospital
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Contacto:
- Xiaowei Wei
- Número de teléfono: +8613813973094
- Correo electrónico: gswxw@126.com
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Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Able to provide written informed consent and voluntarily participate in this study.
- Male or female subjects aged between 18 and 75 years, inclusive.
- Histologically or cytologically confirmed metastatic colorectal adenocarcinoma.
- No prior systemic anti-tumor therapy; patients who have received neoadjuvant/adjuvant therapy are eligible if the time from the last chemotherapy to recurrence or progression is more than 6 months.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Expected survival of at least 3 months.
- Presence of at least one measurable lesion at baseline assessed by the investigator according to RECIST 1.1. Measurable lesions must not have been previously treated with radiotherapy or other local therapy, unless the lesion located in a previously irradiated area has been confirmed to have progressed.
Adequate organ function as defined below (no blood products or hematopoietic growth factors are allowed within 14 days prior to the first dose of study treatment):
- Absolute neutrophil count (ANC) ≥1.5×10^9/L
- Platelet count ≥100×10^9/L
- Hemoglobin ≥9 g/dL
- Serum albumin ≥2.5 g/dL
- Total bilirubin ≤1.5 × ULN; ALT and AST ≤2.5 × ULN, or ≤5 × ULN in the presence of liver metastases
- Serum creatinine ≤1.5 × ULN, or creatinine clearance >60 mL/min (calculated by Cockcroft-Gault formula)
- Activated partial thromboplastin time (APTT) and international normalized ratio (INR) ≤1.5 × ULN. Subjects receiving stable-dose anticoagulation such as low molecular weight heparin or warfarin with INR within the expected therapeutic range are eligible.
- Female subjects of childbearing potential must have a negative serum pregnancy test within 72 hours prior to the first dose of study treatment, must not be breastfeeding, and must agree to use effective contraception (e.g., intrauterine device, contraceptive pills, or condoms) during the study and for at least 6 months after the last dose of study treatment. Male subjects with partners of childbearing potential must be surgically sterile or agree to use effective contraception during the study and for 3 months after the last dose of study treatment, and must not donate sperm during the study period.
Exclusion Criteria:
- Received local radiotherapy within 4 weeks prior to the first dose of study drug, and adverse events due to radiotherapy have not recovered to baseline levels. Subjects who received palliative radiotherapy to peripheral sites (e.g., bone metastases) more than 4 weeks prior to the first dose are eligible, provided they have recovered from any acute adverse reactions.
- Known active central nervous system (CNS) metastases and/or carcinomatous meningitis. Subjects with previously treated brain metastases may participate, provided they have stable brain metastases and have not required steroid treatment for brain metastases for at least 28 days prior to study entry. This exception does not apply to carcinomatous meningitis, which is excluded regardless of clinical stability.
- Major surgery, open biopsy, or severe trauma within 28 days prior to the first dose of study drug.
- History of allergy to any anti-angiogenic agents, any component of monoclonal antibodies, capecitabine, oxaliplatin, or other platinum-based drugs.
- Uncontrolled hypertension despite anti-hypertensive medication (systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg).
- Subjects with uncontrolled cardiovascular clinical symptoms or diseases, including but not limited to: (1) NYHA class II or higher heart failure; (2) unstable angina pectoris; (3) myocardial infarction within the past 1 year; (4) clinically significant supraventricular or ventricular arrhythmias without clinical intervention or still poorly controlled after clinical intervention.
- Significant clinically relevant bleeding symptoms or clear bleeding tendency within 3 months prior to the first dose, such as gastrointestinal bleeding, hemorrhagic gastric ulcer, or vasculitis.
- Arterial/venous thromboembolic events within 6 months prior to the first dose, such as cerebrovascular accidents (including transient ischemic attack, cerebral hemorrhage, cerebral infarction), deep vein thrombosis, and pulmonary embolism. Superficial venous thrombosis may be included at the investigator's discretion.
- Presence of another progressing or actively treated malignancy, except for non-melanoma skin cancer and cervical carcinoma in situ that have received curative treatment.
- Subjects with other factors that, in the investigator's opinion, may lead to premature discontinuation of the study, such as other severe diseases (including psychiatric disorders) requiring concomitant treatment, clinically significant laboratory abnormalities, family or social factors that may affect subject safety or trial data collection.
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)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
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Experimental: Adebrelimab + Chemotherapy + Targeted Therapy + Simvastatin
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Adebrelimab[1200mg i.v, q3w], Capecitabine [1000mg/m² po, bid, d1-d14, q3w], Oxaliplatin [130mg/m² i.v, d1, q3w], Bevacizumab [7.5mg/kg i.v, d1, q3w], Simvastatin [80mg po qd] regimen treatment, 6-8 weeks, then enter the maintenance phase, with oxaliplatin discontinued during the maintenance phase
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¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Investigator-assessed Objective Response Rate(ORR)
Periodo de tiempo: 2 years.
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ORR is the proportion of participants with investigator-assessed complete or partial response per [RECIST 1.1] criteria, with response confirmed on subsequent imaging.
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2 years.
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Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Overall Survival(OS)
Periodo de tiempo: up to 5 years after treatment discontinuation
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OS is the time from treatment initiation to death from any cause.
Patients alive at study end will be censored at their last known contact date.
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up to 5 years after treatment discontinuation
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Progression Free Survival(PFS)
Periodo de tiempo: From treatment initiation until documented disease progression, death, or up to 1 years of follow-up, with survival follow-up conducted every 3 months (±14 days) via telephone after treatment discontinuation.
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PFS is the time from treatment initiation to disease progression or death (whichever comes first), assessed per [RECIST 1.1] criteria.
Patients without events at study end will be censored at their last assessment date.
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From treatment initiation until documented disease progression, death, or up to 1 years of follow-up, with survival follow-up conducted every 3 months (±14 days) via telephone after treatment discontinuation.
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Disease Control Rate(DCR)
Periodo de tiempo: Imaging examinations will be performed every 6 weeks for the first 12 months after initial treatment, then every 12 weeks thereafter through study completion (maximum follow-up of 1 years).
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DCR is the proportion of participants with investigator-assessed CR, PR, or SD per [RECIST 1.1] criteria, with response confirmed on subsequent imaging.
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Imaging examinations will be performed every 6 weeks for the first 12 months after initial treatment, then every 12 weeks thereafter through study completion (maximum follow-up of 1 years).
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Safety (Adverse Events, Vital Signs, Laboratory Parameters, and Quality of Life Assessed Using NCI-CTCAE v5.0)
Periodo de tiempo: From ICF through 100 days after the last dose of study treatment
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From ICF through 100 days after the last dose of study treatment
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Colaboradores e Investigadores
Patrocinador
Patrocinador
Colaboradores
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
Otros números de identificación del estudio
- 2025-SR-692.A2
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.
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