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临床试验/NCT02250014
NCT02250014已完成1 期

The Immuno-Response to Primary Cryotherapy for the Treatment of Prostate Cancer

University of Colorado, Denver2 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2015年10月5日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
19
试验地点
2
主要终点
Change in B cell response identified by Serametrix assay

研究概览

简要总结

This randomized pilot phase I trial studies how well sargramostim after cryotherapy works in treating patients with prostate cancer. Biological therapies, such as sargramostim, use substances made from living organisms that may stimulate the immune system in different ways and stop tumor cells from growing. Cryosurgery, also known as cryotherapy, kills tumor cells by freezing them. Giving sargramostim after cryotherapy may work better in treating prostate cancer.

详细描述

PRIMARY OBJECTIVES:

I. Determine an unknown normal immune response (T cell and B cell) to post-cryotherapy treatment for prostate cancer.

II. Detect the altered immune response (T cell and B cell) post-GM-CSF (sargramostim) response and post-cryotherapy for the prostate cancer.

Patients are randomized to 1 of 2 treatment arms.

ARM I (TREATMENT): Patients undergo cryotherapy on day 0 and receive sargramostim subcutaneously (SC) on days 1, 3, 5, 8, 10, and 12.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Patients diagnosed with prostate cancer that elect to undergo primary cryotherapy of the prostate
  • Patients who are diagnosed with clinical stage T1a -T2c prostate cancer
  • Gleason score sum of less than or equal to 7
  • Prostate-specific antigen (PSA) < 20 ng/dl
  • Patient will read, understand and sign the informed consent and Health Insurance Portability and Accountability Act (HIPAA) agreement
  • Patients must have a life expectancy of at least one year

排除标准

  • Known hypersensitivity to granulocyte macrophage colony stimulating factor (GM-CSF) or yeast
  • Anticipated blood donation within the next 90 days
  • Magnetic resonance imaging (MRI), computed tomography (CT) and bone scan evidence of metastatic prostate cancer regardless the PSA level; (the indication for which is clinically driven and at the discretion of the treating physician)
  • Any history of current or within the past 48 hours of acute or chronic bacterial, fungal or viral infectious disease
  • Documented excessive leukemic myeloid blasts in the bone marrow or peripheral blood (>= 10%) in the past 6 months
  • Previous organ transplant
  • Immunosuppression including primary, secondary, iatrogenic and idiopathic
  • Other serious diseases (hematological, hepatic, renal, respiratory, central nervous system, autoimmune or psychiatric)
  • Enrollment in other studies for any disease in the past 30 days
  • Diagnosis of cancer that in not considered cured, except basal cell carcinoma (BCC) of skin
  • Prior transurethral resection of the prostate with a large tissue defect (at the discretion of the investigator)
  • History of abdominoperineal resection for rectal cancer, rectal stenosis, or other major rectal pathology
  • Patient currently receiving lithium, steroid, chemotherapy or radiotherapy treatment
  • Patients with a Hemoglobin of less than 12%

结局指标

主要结局

Change in B cell response identified by Serametrix assay

时间窗: Baseline to up to 3 months after cryotherapy

A scatter plot of each cytokine and antigen level will be created for each patient by marker to observe the behavior of the markers (rising, falling, flat, or combination over time). Patient specific pre-operative levels will be used to obtain individual baseline measures from which the difference in follow-up cytokine and antigen levels will be calculated, then a simple descriptive comparison of the mean elevation in the markers' levels across cohorts will be graphed.

Change in T cell responses identified by Intracellular cytokine assay and enzyme-linked immunospot

时间窗: Baseline to up to 3 months after cryotherapy

A scatter plot of each cytokine and antigen level will be created for each patient by marker to observe the behavior of the markers (rising, falling, flat, or combination over time). Patient specific pre-operative levels will be used to obtain individual baseline measures from which the difference in follow-up cytokine and antigen levels will be calculated, then a simple descriptive comparison of the mean elevation in the markers' levels across cohorts will be graphed.

次要结局

  • Change in PSA levels in serum samples(Up to 6 months after cryotherapy)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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