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临床试验/NCT02587247
NCT02587247已完成2 期

Apport de l'Immuno-TEP préciblée Avec l'Anticorps bispécifique Anti-ACE x Anti-HSG TF2 et le Peptide IMP-288 marqué au Gallium-68 Pour l'Imagerie Des Patients Potentiellement Candidats à Une Chirurgie d'exérèse et/ou Thermoablation Locale d'Une ou Plusieurs métastases, au Diagnostic ou Lors de la Rechute de Cancers Colo-rectaux (CCR) Exprimant l'antigène Carcino-embryonnaire (ACE): Comparaison au Bilan Conventionnel

Nantes University Hospital4 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2016年3月1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
已完成
入组人数
11
试验地点
4
主要终点
Evaluate the sensitivity of the immuno-PET PET / CT pretargeted with the bispecific anti-CEA x anti-HSG TF2 antibody and IMP-288 peptide labeled with Gallium-68

研究概览

简要总结

Evaluation of the sensitivity of the immuno-PET PET / CT pretargeted with the bispecific anti-CEA x anti-HSG TF2 antibody and IMP-288 peptide labeled with Gallium-68 for imaging potential candidate patients for surgery of local resection of one or more metastases at diagnosis or during relapse CCR expressing CEA.

详细描述

Injection of a bispecific anti-CEA x anti-HSG antibody TF2 (120 nmoles) and 30 hours later IMP-288 peptide labeled with gallium-68 (3 to 6 nmoles/150 MBq). A TEP imaging acquisition is plannified 60 min after the 68-Ga injection.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Existence of one or more metastases of of colorectal cancer (CRC) expressing the CEA , potentially accessible by surgical or thermo resection at the moment of the diagnosis or at relapse.
  • Isolated and progressive elevation of plasma CEA during the monitoring of CRC with high metastatic risk
  • More than 18 years
  • Negative pregnancy test for women of childbearing age. Women of childbearing age should take effective continuous contraception for 3 months.
  • At least 4 weeks after the last treatment and after recovery of potential toxicity
  • Karnofsky more than 70 or ECOG 0-1
  • Life expectancy of at least 6 months
  • CEA positive immunohistochemistry or plasma CEA supperior or equal to the normal level
  • Creatinin less or equal 200 micromol/L
  • Signed informed consent
  • geographical proximity

排除标准

  • Pregnancy or breastfeeding
  • Serious illness or comorbidity assessed risk
  • History of other cancer within 5 years, with the exception of skin carcinomas other than melanomas or in-situ carcinoma of the cervix
  • Anti-antibody presence in patients who have already received antibody
  • Hypersensitivity to antibodies or proteins
  • Intellectual inability to sign the informed consent
  • Insulin-dependent diabetic patient or non-insulin dependent

研究组 & 干预措施

TF2 antibody/68Ga-IMP-288

Experimental

TF2 antibody/68Ga-IMP-288

干预措施: TF2 antibody/68Ga-IMP-288 (Drug)

结局指标

主要结局

Evaluate the sensitivity of the immuno-PET PET / CT pretargeted with the bispecific anti-CEA x anti-HSG TF2 antibody and IMP-288 peptide labeled with Gallium-68

时间窗: Month 3

Initial and M3 imaging assessment comparaison, and/or immunohistochemistry

次要结局

  • To compare the diagnostic performance of immuno-PET with morphological and functional imaging procedures currently performed in the imaging assessment (CT, ultrasound + liver MRI, FDG-PET).(Month 3)
  • To Determine the value of immuno-PET in terms of specificity and predictive value. This determination will be made at the "patient" and at the "injury level.(Month 3)
  • To assess the safety of the procedure(Month 3)
  • Search for the development of a blood Immunization against the products(Month 3)
  • To study the expression of CEA intensity on surgical excision parts in surgical patients and compare it to the semi-quantitative immuno-PET(No more than 3 months (it depend of the day of the surgery))
  • To evaluate the clinical impact (new lecture of imaging, new examens)(M1)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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