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临床试验/NCT05192694
NCT05192694Unknown不适用

Evaluation of Fapi-pet in Prostate Cancer

Helsinki University Central Hospital2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2022年3月10日最近更新:
适应症

试验速览

阶段
不适用
入组人数
40
试验地点
2
主要终点
Positive predictive value on a lesion level

研究概览

简要总结

The investigators explore the biodistribution of FAPI-PET expression in primary high-risk prostate cancer in men undergoing RALP and eLND and in men with metastatic PCa about to start next generation antiandrogen.

详细描述

This is an exploratory cohort study comprised of men with clinically localized or locally advanced high-risk prostate cancer (GG 3-5, cT2-cT3, Nx, M0) managed by RALP and eLND and men with metastatic (mHSPC or mCRPC) prostate cancer scheduled to start NHT along clinical care pathway (e.g., apalutamide, enzalutamide) at HUS Helsinki University Hospital and Helsinki University, Finland.

Men identified along routine clinical care as candidates for the study will be asked to consent.

Once consented, patients will undergo PSMA-PET imaging instead of conventional imaging (CT and bone scan) and experimental FAPI-PET imaging. Furthermore, biomarker samples will be obtained before and after treatment (surgery or novel antiandrogen) and surgical specimen will be processed for routine pathological evaluation and multiplex IHC studies. Serum samples will be tested for PCa biomarkers (e.g., PSA, NSE, CgA) and cfDNA. Urine will be processed and extracellular vesicles (exosomes) isolated and markers of reactive stroma will be sought for.

Radical prostatectomy and novel hormonal treatment will be done according to current recommendations and guidelines in Finland.

Postoperatively, patients will be followed with PSA every six months. Biochemical recurrence will be set at PSA of 0.2 ug/l or higher.

研究设计

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

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Men scheduled for radical prostatectomy
  • Age over 18 years
  • GG 3-5, cT2-cT3, Nx, M0 prostate cancer
  • no contraindication to PSMA - or FAPI-PET
  • willing to undergo study related procedures (imaging and laboratory tests) Men scheduled for novel antiandrogen
  • Age over 18 years
  • GG2-5, cT2-4, N0-1, M1
  • hormone sensitive or castration resistant prostate cancer

排除标准

  • Not willing or capable to undergo study related procedures

结局指标

主要结局

Positive predictive value on a lesion level

时间窗: through study completion, an average of 1 year

Positive predictive value of FAPI-PET on a lesion level using histopathology or confirmatory imaging as ground truth

次要结局

  • Positive predictive value on a patient level(through study completion, an average of 1 year)
  • To assess the biodistribution of FAPI and PSMA PET signal in comparison to histology(through study completion, an average of 1 year)
  • To assess the biodistribution of FAPI and PSMA PET signal in comparison to biomarkers in "wet" samples(through study completion, an average of 1 year)
  • To assess the biodistribution of FAPI PET signal in comparison to PSMA-PET signal(through study completion, an average of 1 year)
  • To assess the biodistribution of FAPI and PSMA PET signal in comparison to immunohistochemistry(through study completion, an average of 1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Antti Rannikko

Assistant professor

Helsinki University Central Hospital

研究点 (2)

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Evaluation of Fapi-pet in Prostate Cancer. | 临床试验