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临床试验/NCT02297386
NCT02297386已完成1 期

Phase I Trial Of [18F] Dihydro-testosterone Pet and MR Imaging In Patients With Localized Prostate Cancer

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2014年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
3
试验地点
1
主要终点
increase in standardize uptake values (SUV) between the second and third FDHT scans

研究概览

简要总结

The purpose of this study is to test the ability of a new PET scan radiotracer, called FDHT (stands for [18F] Dihydro-Testosterone), to better find and monitor prostate cancer. Radiotracers are a type of drug that carries small amounts of radioactivity that can be seen by the PET scanner. FDHT is a radiotracer that looks for a protein which is present in almost all prostate cancer cells. The investigators want to find out if we can find and monitor changes in cancer using a FDHT PET scan.

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
21 Years 至 79 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Male aged 21 years or older and below 80 years of age.
  • Signed written informed consent and willingness to comply with protocol requirements.
  • Histologically confirmed diagnosis of prostate cancer.
  • Staging imaging workup including a baseline MRI of the prostate and pelvis performed at MSKCC.
  • Baseline imaging to rule out distant metastatic disease (99mTc bone scan, NaF PET, total body MRI, or CT chest/abdomen/pelvis)
  • Karnofsky performance status ≥ 70
  • Clinical criteria required to be eligible:
  • a. One of the following i.Pre-treatment PSA ≥10 ng/dL, OR ii. Clinical T-stage assessed by digital rectal exam of ≥T2a, OR ii . Radiographic ≥T3a on MRI, OR iv. Gleason score of ≥3+4=7 c. Visible intraprostatic tumor foci ≥1 cm in largest dimension on T2-weighted images based on initial pre-treatment MRI
  • Physician recommendation of ADT.

排除标准

  • Metastatic disease on standard staging imaging (beyond regional lymph node involvement).
  • o Absence of metastatic disease (beyond regional lymph node involvement) as defined by a negative bone scan, NaF PET, CT chest/abdomen/pelvis, or total body MRI.
  • Prior treatment of the prostate gland for malignant conditions (surgery, cryotherapy, radiotherapy, or photodynamic therapy).
  • Physician prescription of androgen receptor antagonist therapy (examples: bicalutamide, flutamide, or enzalutamide) during time of protocol scans.
  • o Note: ADT consists of chemical castration (i.e. degarelix) to remove endogenous DHT. Androgen receptor antagonists will bind to the androgen receptor and inhibit FDHT from binding.
  • Patients receiving testosterone supplementation .
  • Any contraindication to baseline MRI based on departmental MR questionnaire, or inability to cooperate for an MRI scan.
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to FDHT.
  • Hepatic laboratory values:
  • Bilirubin >1.5 x ULN (institutional upper limits of normal)
  • AST/ALT >2.5 x ULN
  • Albumin <2 g/dL
  • Creatinine >2.5 mg/dL
  • Calcium >11 mg/dL
  • Other serious illness(es) which might preclude completion of this study or interfere with determination of causality of any adverse effects experienced in this study.

研究组 & 干预措施

[18F] DIHYDRO-TESTOSTERONE PET

Experimental

The diagnostic intervention of this study is the use of FDHT PET in localized prostate cancer. Patients will undergo a 30 minute dynamic scan of the pelvis followed by a whole body scan of approximately 30-minutes duration. The dynamic scan will be optional, but strongly encouraged. PET scanning will preferably be done on the GE Discovery STE PET/CT scanner or the equivalent generation of scanner. The PET scans are routinely "quantitative," that is corrected for attenuation and scatter and adjusted for system sensitivity and providing parametric images in terms of standardized uptake values (SUV) (= μCi found/gm tissue / μCi injected/gm body mass).

干预措施: [18F] DIHYDRO-TESTOSTERONE (Drug)

[18F] DIHYDRO-TESTOSTERONE PET

Experimental

The diagnostic intervention of this study is the use of FDHT PET in localized prostate cancer. Patients will undergo a 30 minute dynamic scan of the pelvis followed by a whole body scan of approximately 30-minutes duration. The dynamic scan will be optional, but strongly encouraged. PET scanning will preferably be done on the GE Discovery STE PET/CT scanner or the equivalent generation of scanner. The PET scans are routinely "quantitative," that is corrected for attenuation and scatter and adjusted for system sensitivity and providing parametric images in terms of standardized uptake values (SUV) (= μCi found/gm tissue / μCi injected/gm body mass).

干预措施: PET scan (Device)

[18F] DIHYDRO-TESTOSTERONE PET

Experimental

The diagnostic intervention of this study is the use of FDHT PET in localized prostate cancer. Patients will undergo a 30 minute dynamic scan of the pelvis followed by a whole body scan of approximately 30-minutes duration. The dynamic scan will be optional, but strongly encouraged. PET scanning will preferably be done on the GE Discovery STE PET/CT scanner or the equivalent generation of scanner. The PET scans are routinely "quantitative," that is corrected for attenuation and scatter and adjusted for system sensitivity and providing parametric images in terms of standardized uptake values (SUV) (= μCi found/gm tissue / μCi injected/gm body mass).

干预措施: MRI (Device)

[18F] DIHYDRO-TESTOSTERONE PET

Experimental

The diagnostic intervention of this study is the use of FDHT PET in localized prostate cancer. Patients will undergo a 30 minute dynamic scan of the pelvis followed by a whole body scan of approximately 30-minutes duration. The dynamic scan will be optional, but strongly encouraged. PET scanning will preferably be done on the GE Discovery STE PET/CT scanner or the equivalent generation of scanner. The PET scans are routinely "quantitative," that is corrected for attenuation and scatter and adjusted for system sensitivity and providing parametric images in terms of standardized uptake values (SUV) (= μCi found/gm tissue / μCi injected/gm body mass).

干预措施: Blood draw (Other)

结局指标

主要结局

increase in standardize uptake values (SUV) between the second and third FDHT scans

时间窗: 1 year

Enrolling 15 patients will provide 80% power to detect a 33% increase in the mean uptake (from 6 to 8) between the 2nd and the 3rd scans.

次要结局

  • correlate AR expression to FDHT uptake(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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