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临床试验/NCT02608203
NCT02608203已完成2 期

Impact of [68 Ga]-DOTANOC PET-CT on the Management of Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs): Prospective, Multicentric Study.

Assistance Publique Hopitaux De Marseille1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2016年5月26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
18
试验地点
1
主要终点
level of changes (%) between care management before DOTANOC PET and care management after DOTANOC PET

研究概览

简要总结

Somatostatin receptors are overexpressed in GEP-NETs and can be visualized in vivo by radiolabeled somatostatin-analogs.

During the last decades, conventional scintigraphy using 111In-DTPA-Octreotide (often named somatostatin receptor scintigraphy or SRS) was considered as the gold standard nuclear imaging technique in the evaluation of GEP-NETs. However, SRS may be suboptimal in this clinical setting because of the low intrinsic resolution of the technique and its selectivity for SST2 only. Its overall sensitivity is estimated to 60-70% (per lesion analysis), even when using the most recent SPECT-CT cameras. MRI have also a higher sensitivity than CT and SRS for the detection of liver metastases from GEP-NETs.

In recent years, positron emission tomography (PET) imaging, a high resolution and sensitive technology, has gained an increasing role in oncology. It has also been evaluated in GEP-NETs with somatostatin agonists (SSTa) radiolabelled with Gallium-68 [68Ga], a positron emitter with very promising results. Its diagnostic sensitivity is clearly superior to SRS and many European centers have already replaced SRS by [68Ga]-PET-SSTa.

Currently, three different [68Ga]-coupled peptides can be used in trials: DOTA-TOC, DOTA-TATE and DOTA-NOC with excellent affinities for SST2 (IC50: 2.5; 0.2 and 1.9 nM, respectively). Sensitivities of DOTA-TOC and DOTA-TATE PET/CT are quite similar.

[68Ga]-DOTANOC which also binds to SST5 was recently found to detect significantly more lesions than the SST2-specific radiotracer [68Ga]-DOTATATE in patients with GEP-NETs but this requires further evaluation.

It is therefore important to determine the interest of [68Ga]-DOTANOC combined with the standard diagnosis strategy in GEP-NETs and evaluate medicoeconomic impact of adding [68Ga]-DOTANOC in the work-up of patients.

The investigators hypothesis is that [68Ga]-DOTANOC will modify the management in at least 20% of patients in a more adapted way according to the 2012 ENETS guidelines in comparison to the decision based on the standard imaging work up (multiphasic WB CT, liver MRI and SRS).

110 patients will be included prospectively in 5 different French experienced centers (Marseille, Bordeaux, Toulouse, Paris, Clermond-Ferrand).

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

  • Age> 18 years, with affiliation to the Social Security.
  • Written consent of the patient.
  • Patients with any of the following 5 situations:
  • GEPs without metastasis.
  • GEPs with unilateral liver metastases candidates to unilateral hepatectomy.
  • GEPs with unknown primary tumor.
  • GEPS with livers metastases candidates to liver transplantation.
  • Metastatic GEPs with grade 1 or 2 tumour and negative SRS.
  • Reference imaging within the last 3 months : multiphasic total body CT scan, liver MRI and SRS (SPECT/CT).

排除标准

  • minor subject.
  • Pregnant or breast-feeding.
  • Absence of therapeutic alternatives in metastatic GEP.
  • Undifferentiated GEP and/or metastatic GEPs with grade 3 tumours.

研究组 & 干预措施

patients with gastroenteropancreatic neuroendocrine tumors

Experimental

干预措施: [68Ga]-DOTANOC PET/CT (Drug)

结局指标

主要结局

level of changes (%) between care management before DOTANOC PET and care management after DOTANOC PET

时间窗: 6 months

次要结局

  • Positive predictive values of DOTANOC PET and standard imaging(1 year)
  • negative predictive values of DOTANOC PET and standard imaging(1 year)
  • correlation between tumor type and DOTANOC PET results(1 year)
  • number of patients for whom PET allowed the detection of lesions not described by standard imaging(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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