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临床试验/NCT06852638
NCT06852638招募中2 期

CD70-targeted PET/ CT in the Diagnosis of Malignant Cancers

RenJi Hospital2 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2024年12月23日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
300
试验地点
2
主要终点
Standardized uptake value (SUV) of normal tissues and organs.

研究概览

简要总结

This study aims to determine the value of cluster of differentiation (CD70)-targeted immuno-positron emission tomography/computed tomography (immunoPET/CT) imaging for diagnosing human malignancies, including renal cell carcinoma (particularly clear cell renal cell carcinoma), lymphoma, and nasopharyngeal carcinoma (NPC), among others.

详细描述

Histologically confirmed malignant cancers (renal cancer (especially clear cell renal cell carcinoma), lymphoma, or nasopharyngeal carcinoma (NPC)) or patients with suspected malignant cancers (renal cancer (especially clear cell renal cell carcinoma), lymphoma, or nasopharyngeal carcinoma (NPC)) indicated by conventional diagnostic imaging will be included. Patients will also be included for routine follow-up, surveillance, and evaluation of treatment efficacy following the initial CD70-targeted immunoPET/CT imaging.

Enrolled patients will undergo whole-body immunoPET/CT scans 1-2 hours after tracer injection (0.01-0.1 mCi/kg). Uptake of imaging tracers in tumors and normal organs/tissues will be scored both visually and quantitatively.

Tumor uptake will be quantified using the maximum standard uptake value (SUVmax). Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy will be calculated to assess diagnostic efficacy. The correlation between lesion uptake and CD70 expression levels, as determined by immunohistochemical staining, will be further analyzed. The primary exploratory endpoint will be the imaging feasibility of the tracers and their preliminary diagnostic value compared with conventional imaging approaches such as 18F-FDG PET/CT, CT/MRI. The secondary endpoint is the impact of CD70-targeted immunoPET/CT imaging on clinical decision-making.

研究设计

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18-80 year-old and of either sex;
  • Histologically confirmed diagnosis of renal cancer (especially ccRCC)/lymphoma/NPC or suspected renal cancer/lymphoma/NPC by diagnostic imaging;
  • Capable of giving signed informed consent, including compliance with the requirements and restrictions in the informed consent form (ICF) and this protocol.

排除标准

  • Pregnancy;
  • Severe hepatic and renal insufficiency;
  • Allergic to single-domain antibody radiopharmaceuticals.

研究组 & 干预措施

CD70-targeted immunoPET imaging

Experimental

Enrolled patients will undergo a CD70-targeted immunoPET/CT scanning.

干预措施: [18F]F-RESCA-RCCB6 (Drug)

CD70-targeted immunoPET imaging

Experimental

Enrolled patients will undergo a CD70-targeted immunoPET/CT scanning.

干预措施: [18F]F-RESCA-R8B4 (Drug)

CD70-targeted immunoPET imaging

Experimental

Enrolled patients will undergo a CD70-targeted immunoPET/CT scanning.

干预措施: [18F]F-RESCA-RD06 (Drug)

CD70-targeted immunoPET imaging

Experimental

Enrolled patients will undergo a CD70-targeted immunoPET/CT scanning.

干预措施: [68Ga]Ga-NOTA-R8B4 (Drug)

CD70-targeted immunoPET imaging

Experimental

Enrolled patients will undergo a CD70-targeted immunoPET/CT scanning.

干预措施: [68Ga]Ga-NOTA-RD06 (Drug)

结局指标

主要结局

Standardized uptake value (SUV) of normal tissues and organs.

时间窗: 1 day from injection of the tracers

Measurement of the overall biodistribution of the above tracers in normal tissues and organs (bladder (after voiding), background (pelvic fat), blood, brain, salivary and lacrimal glands, lung, liver, spleen, pancreas, small intestine, and kidneys). To calculate the SUV, circular regions of interest were drawn around the area of focally increased uptake in the transaxial slices and automatically fitted to a three-dimensional volume of interest.

SUV of tumors

时间窗: 1 day from injection of the tracers

The SUV of the above tracers in the primary and/or metastatic lesions of the included subjects. To calculate the SUV, circular regions of interest were drawn around the area of focally increased uptake in the transaxial slices and automatically fitted to a three-dimensional volume of interest.

Radiation dosimetry of tissues/organs

时间窗: 1 day from injection of the tracers

Measurement of absorbed radiation doses (Gy/MBq) to tissues/organs. The following tissues were included: adrenals, brain, breasts, gallbladder, small intestine, upper and lower large intestine, stomach, heart contents, heart muscle, kidney, liver, lung, muscle, ovaries, pancreas, red marrow, trabecular and cortical bone, spleen, testes, thymus, thyroid, urinary bladder, and uterus. Dynamic imaging within one hour will be performed for this purpose.

Radiation dosimetry of tumors

时间窗: 1 day from injection of the tracers

Measurement of absorbed radiation doses (Gy/MBq) to tumors. Dynamic imaging within one hour will be performed for this purpose.

Radiation dosimetry of whole-body

时间窗: 1 day from injection of the tracers

Whole-body activity was measured using a large volume of interest (VOI) covering the entire subject.

Diagnostic sensitivity

时间窗: 30 days

Sensitivity = (True Positives) / (True Positives + False Negatives). The diagnostic value of CD70 immunoPET/CT will be compared with that of conventional imaging approaches, including 18F-FDG PET/CT, CT, and MRI.

Diagnostic specificity

时间窗: 30 days

Specificity = (True Negatives) / (True Negatives + False Positives). The diagnostic value of CD70 immunoPET/CT will be compared with that of conventional imaging approaches, including 18F-FDG PET/CT, CT, and MRI.

Accuracy

时间窗: 30 days

Accuracy = (True Positives + True Negatives) / (Total Tests). The diagnostic value of CD70 immunoPET/CT will be compared with that of conventional imaging approaches, including 18F-FDG PET/CT, CT, and MRI.

Positive Predictive Value (PPV)

时间窗: 30 days

PPV = (True Positives) / (True Positives + False Positives). The diagnostic value of CD70 immunoPET/CT will be compared with that of conventional imaging approaches, including 18F-FDG PET/CT, CT, and MRI.

Negative Predictive Value (NPV)

时间窗: 30 days

NPV = (True Negatives) / (True Negatives + False Negatives). The diagnostic value of CD70 immunoPET/CT will be compared with that of conventional imaging approaches, including 18F-FDG PET/CT, CT, and MRI.

次要结局

  • CD70 immunoPET/CT in altering initial staging for patients with renal cancer/lymphoma/NPC(3-6 months)
  • CD70 immunoPET/CT for postoperative surveillance for patients with renal cancer/lymphoma/NPC(3-6 months)
  • CD70 immunoPET/CT for restaging for patients with renal cancer/lymphoma/NPC(3-6 months)
  • CD70 immunoPET/CT in evaluating treatment responses(1-2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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