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临床试验/NCT04717674
NCT04717674招募中2 期

An Investigation of Short-chain Fatty Acid Uptake in Solid Tumours as Assessed by [18F]Fluoropivalate Positron Emission Tomography and Its Relationship With Tumour Proliferation

University College, London3 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2021年12月7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
21
试验地点
3
主要终点
The relationship between [18F]FPIA uptake and percent positive tumour cells reported as counts defined per area from whole section immunohistochemistry for PHH3.

研究概览

简要总结

The study will be a phase 2, open-label study in patients with solid tumours to explore the relationship between short-chain fatty acid uptake using [18F]FPIA PET/CT and tumour proliferation

详细描述

Cancers have increased energy demands to allow for their rapid growth compared to healthy cells. Glucose is the main source of energy for many cells in the body, and clinicians routinely use a scan which looks at glucose metabolism to assess if cancer treatment is working. However, some cancer cells can create energy to survive and grow in a different way, using fatty acids. In this study, the investigators are using a PET/CT scan to look at a variety of cancer types to see which cancers use fatty acids for energy and if this can be measured. The PET/CT scan will be carried out twice on 2 separate visits so that the investigators can check that both scans give the same result.

The investigators will also carry out special tests on the tumour tissue taken during routine cancer surgery. These tests will look for specific substances in the cancer cells that are related to cancer biology and growth. The investigators will then compare the results from the surgical tissue to the results of the scan to see if there is a relationship between them.

The study will look at 21 patients with solid tumours conducted in 4 NCITA accredited centres, which have different strengths in recruiting specific patient/tumour-type cohorts. Each patient will have two scan visits (between 2-15 days apart) prior to any new treatment starting to check that the scan measurements are repeatable.

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

  • Patients with radiological evidence of solid primary or metastatic target tumour lesions and the following characteristics will be recruited:
  • Age ≥18 years of age
  • Radiologically confirmed tumour size ≥15mm (at least one lesion must be extra-hepatic)
  • The participant is due to undergo surgery within 3 months of the first [18F]FPIA PET/CT
  • There is time to complete the two research PET studies without any delay to surgery
  • WHO performance status 0 -2
  • If female, the participant is either post-menopausal (>1 year), or surgically sterilised (has had a documented bilateral oophorectomy and/or documented hysterectomy, >2 years), or if of childbearing potential, must have a negative urine pregnancy test within 2 hours prior to injection of imaging agent
  • The participant is able and willing to comply with study procedures, and signed and dated informed consent is obtained.
  • eGFR of ≥30 within 3 months of [18F]FPIA injection.
  • The participant is not scheduled to start cancer treatment (e.g. chemotherapy, radiotherapy, biological therapy or immunotherapy) within the study scanning period.

排除标准

  • The participant has received chemotherapy, immunotherapy, biologic therapy or investigational therapy within 14 days or five half-lives of a drug (whichever is longer) prior to the first dose of [18F]FPIA injection or is due neoadjuvant therapy between the PET and surgery.
  • The participant is pregnant or lactating.
  • The participant is scheduled to have a nuclear medicine or contrast scan within 24 hours before the administration of [18F]FPIA.
  • Participants with claustrophobia or who are unable to comfortably tolerate the scanning procedure.

研究组 & 干预措施

Drug: [18F]Fluoropivalate ([18F]Fluoro-2,2-Dimethylpropionic Acid) (FPIA)

Experimental

Participants will undergo two PET/CT scans with the tracer [18F]Fluoropivalate ([18F]Fluoro-2,2-Dimethylpropionic Acid) (FPIA), referred to as [18F]FPIA, on 2 separate visits.

干预措施: [18F]Fluoropivalate ([18F]Fluoro-2,2-Dimethylpropionic Acid) (Drug)

Drug: [18F]Fluoropivalate ([18F]Fluoro-2,2-Dimethylpropionic Acid) (FPIA)

Experimental

Participants will undergo two PET/CT scans with the tracer [18F]Fluoropivalate ([18F]Fluoro-2,2-Dimethylpropionic Acid) (FPIA), referred to as [18F]FPIA, on 2 separate visits.

干预措施: PET/CT (Procedure)

结局指标

主要结局

The relationship between [18F]FPIA uptake and percent positive tumour cells reported as counts defined per area from whole section immunohistochemistry for PHH3.

时间窗: 6 months

To explore the relationship between short-chain fatty acid uptake using \[18F\]FPIA PET/CT and tumour proliferation in patients with solid tumours.

次要结局

  • Estimation of SUVmax of target lesions at 30 minutes and 60 min.(60 min)
  • Estimation of tumour-to-background ratio of target lesions at 30 minutes and 60 min.(60 min)
  • Graphical presentation and reliability of repeat semi-quantitative measure (SUV) of target lesions between two PET scans for each time point (30 min and 60 min). Bland Altman and ICC will be presented.(15 days)
  • Graphical presentation of [18F]FPIA uptake and whole section immunohistochemistry for Ki-67 and mitotic count (mitoses per mm2) assessed on hematoxylin and eosin (H&E) sections. Pearson's correlation coefficient will be reported.(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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