跳至主要内容
临床试验/NCT04341740
NCT04341740终止不适用

Investigating Marrow Infiltrating Lymphocytes as a Source of Adoptive Cellular Therapy in Renal Cell Carcinoma and Urothelial Carcinoma

University of Oklahoma2 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2020年7月22日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
6
试验地点
2
主要终点
Proportion of subjects with successful isolation and ex-vivo expansion of MILs

研究概览

简要总结

The purpose of this research is to collect health-related information as well as bone marrow and blood specimens to determine if a new form of treatment for patients with kidney and bladder cancer may be possible.

详细描述

This research will collect specimens from the bone marrow and blood to determine if a new treatment for kidney or bladder cancer may be possible. This research study will collect a bone marrow sample as well as a blood sample.

Participation in the research study will last approximately 60 days which includes time to determine if the patient is eligible to participate in the study, perform the research procedures and follow-up with the patient following the research procedures to determine if they are experiencing any side effects. Participation will end approximately 30 days following the bone marrow collection.

The bone marrow and blood samples will be collected from all patients in both cohorts only at a single time point, after they have been enrolled on the study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

入选标准

  • Age ≥18 years
  • Histologically-confirmed, locally advanced unresectable or metastatic RCC (cohort A) or UC (cohort B).
  • ECOG performance status of ≤1
  • Adequate bone marrow function:
  • Platelet count ≥ 100 × 10^9/L
  • ANC ≥ 1.0 ×10^9/L
  • Lymphocyte count ≥ 0.5 ×10^9/L
  • Willingness to undergo bone marrow aspiration (BMA)

排除标准

  • Prior hematopoietic stem cell transplantation
  • Prior radiation to the pelvic region
  • Use of systemic corticosteroids within 28 days of BMA
  • History of another primary malignancy that has been diagnosed or required therapy within the past 2 years (except completely resected basal cell and squamous cell skin cancer, curatively treated localized prostate cancer, and completely resected carcinoma in situ of any site).
  • Presence of an autoimmune disease (e.g., rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosis) requiring active systemic treatment. If the autoimmune disease has been treated, it must be stable clinically. (Hypothyroidism without evidence of Grave's disease or Hashimoto's thyroiditis is not considered an exclusion criterion.)
  • Pregnant females as documented by a serum beta human chorionic gonadotropin (β-hCG) pregnancy test consistent with pregnancy, obtained within 21 days of BMA
  • Infection requiring treatment with antibiotics, antifungal, or antiviral agents within 7 days of BMA
  • Known diagnosis of HIV or CMV infection or active viral hepatitis
  • Administration of hematopoietic growth factor support within 14 days before bone marrow aspiration
  • Chemotherapy administration within 28 days of BMA
  • Unwilling or unable to comply with the protocol
  • Prior or ongoing clinically significant illness, medical condition, surgical history, physical finding, or laboratory abnormality that, in the Investigator's opinion, could affect the safety of the subject.

结局指标

主要结局

Proportion of subjects with successful isolation and ex-vivo expansion of MILs

时间窗: 30 days

A successful expansion will be greater than or equal to 50% viable and greater than or equal to 50% CD3 positive.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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