A Pilot Study of Active Immunotherapy With Carcinoembryonic Antigen Peptide-Pulsed, Autologous Human Cultured Dendritic Cells in Patients With Resected, Stage I, II and III Pancreatic Adenocarcinoma Expressing Carcinoembryonic Antigen
试验速览
- 阶段
- 1 期
- 状态
- 终止
- 发起方
- 入组人数
- 8
- 试验地点
- 2
- 主要终点
- Progression Free Survival
研究概览
简要总结
Rational: White blood cells that have been treated with carcinoembryonic antigen peptide-1 may help the body build an immune response to and kill tumor cells that express CEA.
Purpose: Phase II trial to study the effectiveness of white blood cells plus carcinoembryonic antigen peptide-1 in treating patients with stage I, stage II, or stage III pancreatic cancer that has been surgically removed.
详细描述
Objective
I. Perform a pilot study of active immunotherapy with autologous dendritic cells pulsed with the CEA peptide, CAP-1, after surgical resection in patients with CEA expressing pancreatic cancer. II. Perform laboratory analysis to monitor the presence, persistence, and function of CAP-1 specific T-cells in this patient population.
Outline: Patients undergo leukapheresis for up to 4.5 hours prior to vaccination. Half of the collected dendritic cells are pulsed with carcinoembryonic antigen (CEA) peptide and the other half are pulsed with hepatitis B antigen peptide (HBsAg). Equal doses of CEA and HBsAg peptide pulsed dendritic cells are administered intravenously over 3 minutes every 4 weeks for a total of 6 doses each. Patients undergo a second leukopheresis 2 weeks after the last dose of immunotherapy to obtain specimens for immunologic tests. Patients are followed at weeks 22, 36, 48, and every 6 months thereafter.
Project Accrual: A total of 24 patients will be accrued for this study over 2 years.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Disease Characteristics:
- •Histologically confirmed stage I, II, or III adenocarcinoma of the pancreas Resected with no gross residual disease At least 50% of tumor cells must be CEA positive and stain with at least moderate intensity HLA-A2 positive
- •Patient Characteristics:
- •Age: 18 and over
- •Performance status: Karnofsky 70-100%
- •Life expectancy: Greater than 6 months
- •Hematopoietic: Absolute neutrophil count at least 1000/mm3
- •Hepatic: Bilirubin less than 2.0 mg/dL SGOT and alkaline phosphatase less than 4 times the upper limit of normal No hepatic failure
- •Renal: Creatinine less than 2.0 mg/dL OR Creatinine clearance greater than 50 mL/min
- •Cardiovascular: No New York Heart Association class III or IV heart disease
- •Pulmonary: No concurrent asthma or chronic obstructive pulmonary disease
- •No other malignancy except nonmelanoma skin cancer or controlled superficial bladder cancer within the past 5 years.
- •No history of autoimmune diseases such as inflammatory bowel disease, systemic lupus erythematosus, ankylosing spondylitis, scleroderma, rheumatoid arthritis, or multiple sclerosis
- •No active acute or chronic infection such as urinary tract infection, HIV, or viral hepatitis
- •No active infectious enteritis or eosinophilic enteritis Not pregnant or nursing Fertile patients must use effective contraception
- •Prior Therapy:
- •Biologic therapy: At least 4 weeks since immunotherapy. No other concurrent immunotherapy
- •Chemotherapy: At least 4 weeks since chemotherapy and recovered. No concurrent chemotherapy
- •Endocrine therapy: No concurrent corticosteroid or immunosuppressive therapy. At least 6 weeks since steroid therapy
- •Radiotherapy: At least 4 weeks since radiotherapy and recovered
- •Surgery: Recovered from prior surgery
排除标准
- 未提供
结局指标
主要结局
Progression Free Survival
次要结局
未报告次要终点