Phase II, Open-Label Trial in Patients With Stage IV Malignant Melanoma Using Melaxin as a Cancer Vaccine in Conjunction With BCG
试验速览
- 阶段
- 1 期
- 状态
- 终止
- 入组人数
- 3
- 试验地点
- 2
- 主要终点
- Safety as Measured by Number of Participants With Unexpected Adverse Events or Unexpected Laboratory Results.
研究概览
简要总结
The purpose of this study is to determine if treatment with the autologous cellular vaccine, Melaxin, in combination with Bacillus Calmette-Guerin (BCG) injections is effective in Stage IV malignant melanoma.
详细描述
Chemotherapy and immunotherapy are the main therapies for metastatic melanoma with the hope of prolonging survival. The ideal immunotherapy would consist of the professional antigen-presenting cell, the dendritic cell, with the entire repertoire of tumor antigens inside. The best way to achieve this is by creating an autologous hybrid fusion cell of the dendritic cell and tumor cell. In this study, melanoma tumor tissue surgically removed from the patient will be disassociated into single cells, irradiated and fused to dendritic cells produced by culturing the patient's blood monocytes. Prior to the electrofusion procedure, the tumor cells are stained red and the dendritic cells are stained green. After fusion, the uniquely colored fused cells, or dendritomas, are separated from the unfused cells by use of a fluorescence activated cell sorter. This highly purified population is then divided into 4 doses containing 250,000 dendritomas each and frozen. Each dose is thawed, diluted to 1 milliliter (ml) with Sterile Saline for Injection containing 5 percent (%) human serum albumin and administered subcutaneously (SQ) over a lymph node bed to the patient once every 4 weeks. A separate injection of Bacillus Calmette-Guerin (BCG) is administered in the same area within 10 minutes of the dendritoma injection. The safety and efficacy of the therapy will be evaluated in 25 patients.
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
- •Ability to give informed consent
- •Male or female patient whose age is > 18 years of age
- •Histological documented Stage IV malignant melanoma (American Joint Committee on Cancer (AJCC) sixth edition)
- •Pathology report from tumor specimen verifying melanoma diagnosis
- •Free of infection
- •Hemoglobin> 9.0 grams per deciliter (gm/dL), White Blood Cells (WBC) >3000/ cubic millimeters (mm3), platelets> 100,000mm3
- •Liver function test that are less than 2 times the upper limit of normal of the reference range for the testing laboratory
- •Adequate cardiac function-any evidence of ischemic heart disease demonstrated by history, physical, or EKG will require referral to a cardiologist for evaluation and clearance prior to protocol therapy
- •No immunotherapy within the past 3 months
- •A minimum of 4 doses of lot-released, autologus Melaxin (1.0 million dendritomas)
排除标准
- •Other malignancies in the past 5 years with the exception of non-melanoma skin cancer or carcinoma in situ of the cervix
- •Has received any immunosuppressive agent within 30 days prior to treat
- •Creatinine> 2.5 milligrams per deciliter (mg/dL) or currently on dialysis
- •Positive serum pregnancy test, breast-feeding,or planning to conceive or father or father a child in the period surrounding the study as described in the informed consent.
- •Women of childbearing potential who cannot follow the directions for birth control
- •Eastern Cooperative Oncology Group (ECOG) performance status greater than 3
- •Positive Rdonr panel (Human Immunodeficiency virus (HIV) 1, 2; Human T-lymphotropic virus (HTLV-1,2); Hepatitis B and C)
- •History of a seizure disorder
- •Brain metastases that have progressed within the last 6 months
- •No measurable disease
结局指标
主要结局
Safety as Measured by Number of Participants With Unexpected Adverse Events or Unexpected Laboratory Results.
时间窗: From first vaccine to 18 months after the last injection
Expected adverse events included injection site reactions, fever, chills, and arthralgias as anticipated with vaccine therapy. No unexpected or uncommon adverse events occurred such as disseminated sepsis. Clinical laboratory results on all participants were within expected ranges, including an increase in the number of IFN gamma expressing T-cells.
次要结局
- Tumor Response Measured by RECIST Criteria and Progression-free Survival.(From first vaccine to 18 months after the last injection)
