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临床试验/NCT05000372
NCT05000372已完成1 期

68Ga-grazytracer PET/CT of Tumor Responses to Immunotherapy in Subjects with Solid Tumor or Lymphoma

Peking University Cancer Hospital & Institute1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2021年9月22日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
24
试验地点
1
主要终点
Biodistribution of 68Ga-grazytracer

研究概览

简要总结

This is an open-label positron emission tomography/computed tomography (PET/CT) study to investigate the safety and clinical predictive value of 68Ga-grazytracer in subjects with solid tumor or lymphoma receiving immunotherapy.

详细描述

The investigators recently developed a granzyme B-specific radiotracer named 68Ga-grazytracer. This clinical trial aims to investigate whether granzyme B PET imaging using 68Ga-grazytracer could early identify tumor responses to immune checkpoint inhibitory therapy or CAR-T therapy in subjects with solid tumor and lymphoma. PET/CT imaging of 68Ga-grazytracer will be performed in subjects after immunotherapy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Sequential
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participants who were diagnosed with malignant tumors;
  • Patients who were scheduled to receive immunotherapy based on a decision made by a multidisciplinary team;
  • participants who had no prior immunotherapy;
  • participants who had no regional therapy within 3 months;
  • Participants aged ≥18 years.

排除标准

  • participants with a concurrent disease that would impede the treatment regimen;
  • Participants who were unable or unwilling to provide written informed consent.

研究组 & 干预措施

Feasibility and safety of 68Ga-grazytracer

Experimental

The purpose of the study is to evaluate the safety and early predictive performance of 68Ga-grazytracer for immunotherapy.

干预措施: 68Ga-grazytracer (Drug)

结局指标

主要结局

Biodistribution of 68Ga-grazytracer

时间窗: 3 year

The distribution of 68Ga-grazytracer in tumors and healthy tissues will be examined through total-body dynamic PET/CT imaging.

Incidence of 68Ga-grazytracer-emergent Adverse Events

时间窗: 3 year

Any adverse events following the administration of the radiotracer will be monitored.

Assessing the early predictive value of 68Ga-grazytracer for immunotherapy response

时间窗: 3 year

Participants will be categorized into groups with high or low 68Ga-grazytracer uptake in tumor lesions. The progression-free survival and treatment response, as assessed by RECIST 1.1 criteria, will be compared across these groups.

Analyzing the in vivo granzyme B-specificity of 68Ga-grazytracer

时间窗: 3 year

The specificity of 68Ga-grazytracer will be validated by correlating the immunohistochemistry results of granzyme B in either surgical or biopsy tissue samples with the standardized uptake values (SUV) of 68Ga-grazytracer in the tumors.

次要结局

  • Correlation analysis of 68Ga-grazytracer uptake and tumor immune phenotype(3 year)

研究者

发起方
Peking University Cancer Hospital & Institute
申办方类型
Other
责任方
Sponsor

研究点 (1)

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