Castration-resistant Prostate Cancer Clinical Trial
Official title:
Gadoxetate Sodium Enhanced Magnetic Resonance Imaging (MRI) as a Biomarker for Aggressive Prostate Cancer
The purpose of this research study is to test to see if Gadoxetate Sodium is a useful contrast agent for detecting prostate cancer during magnetic resonance imaging (MRI). Gadoxetate Sodium is an FDA approved contrast agent that is currently used to detect liver cancer. Gadoxetate Sodium shows promise in identifying more aggressive prostate cancers at earlier stages. The study will also test to see if specific genes are expressed in the left over tissue samples from previous prostate fusion biopsy. The investigators hypothesize that Gadoxetate Sodium-enhanced MRI can differentiate aggressive prostate cancer and predict its early recurrence.
A substantial body of evidence implicates androgen hormones, such as testosterone, play a key
role in aggressive prostate carcinogenesis, and much work has been done to evaluate the
relationship between the concentration of testosterone and clinical outcome of patients with
prostate cancer. Several uptake transporters localized to the cell membrane have shown to
enhance steroid hormone uptake, and these same transporters are also expressed within the
prostate where they could increase the capability of neoplastic cells to use testosterone.
One group of uptake carriers is the organic anion-transporting polypeptide (OATP) superfamily
encoded by SLCO genes. OATPs are localized to normal human hepatocytes. OATP1B3, a member of
this family, is also expressed by cancer cells derived from aggressive prostate cancer.
Studies have shown that in prostate cancer, testosterone uptake by cells occurs via OATP1B3,
and its presence increases from undetectable levels in normal prostatic tissue and benign
hyperplasia to marked expression in aggressive prostate cancer.
Current prostate cancer (PCa) diagnosis methods have false positives and are limited in
predicting cancer recurrence. Gadoxetate Sodium is a magnetic resonance imaging agent which
is FDA-approved gadolinium chelate for detecting hepatocellular carcinoma, as normal
hepatocytes express OATP1B3 while most hepatocellular carcinomas do not. Gadoxetate Sodium
acts as a substrate for OTAP1B3, therefore, OATP1B3 positive prostate tumors can potentially
be visualized on MR imaging. Making this contrast agent useful in the evaluation of OATP1B3
status in patients with aggressive PCa and potentially serve as a prognostic and treatment
biomarker.
The investigators hypothesize that Gadoxetate Sodium -enhanced MRI can differentiate
aggressive PCa and predict its early recurrence. The investigators aim to enroll 50 patients
and sort them into localized or metastatic PCa, based on tumor grade. Subjects that agree to
participate will be scheduled for a research pelvic MRI with the Gadoxetate Sodium contrast
within 3 weeks of their office visit. The procedure is be conducted as a standard pelvic MRI
but instead of gadolinium contrast being administered, Gadoextate Sodium will be dosed at
0.1/mL per kilogram of body weight (as prescribed on the contrast label). Once the subject
has undergone the research MRI scan using Gadoxetate Sodium, the MRI and assigned enhancement
ratios will be reviewed. Contrast enhancement ratios (CERs) will be calculated to evaluate
the difference in the degree of enhancement between the tumors and normal tissue. Subject
demographic information, medical history and enhancement ratios will be recorded in the study
database.
Previously obtained remnant biopsy samples from enrolled subjects will be used for
transcriptome and epigenome profiling using genome-wide and targeted gene approaches.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03554317 -
COMbination of Bipolar Androgen Therapy and Nivolumab
|
Phase 2 | |
Active, not recruiting |
NCT03170960 -
Study of Cabozantinib in Combination With Atezolizumab to Subjects With Locally Advanced or Metastatic Solid Tumors
|
Phase 1/Phase 2 | |
Completed |
NCT00974311 -
Safety and Efficacy Study of MDV3100 in Patients With Castration-Resistant Prostate Cancer Who Have Been Previously Treated With Docetaxel-based Chemotherapy
|
Phase 3 | |
Active, not recruiting |
NCT03700099 -
Biomarker Analysis of Castration-resistant Prostate Cancer Undergoing Treatment With Docetaxel Followed by Enzalutamide
|
Phase 2 | |
Completed |
NCT02124668 -
A Study to Monitor the Safety of Enzalutamide in Patients With Progressive Castration-Resistant Prostate Cancer Previously Treated With Docetaxel-Based Chemotherapy
|
Phase 2 | |
Completed |
NCT01634061 -
Phase Ib of Abiraterone Acetate Plus BEZ235 or BKM120 in Castration-resistant Prostate Cancer (CRPC) Patients
|
Phase 1 | |
Completed |
NCT01338831 -
Phase I Study of LFA102 in Patients With Prolactin Receptor-positive Castration-resistant Prostate Cancer or Prolactin Receptor-positive Metastatic Breast Cancer
|
Phase 1 | |
Terminated |
NCT03652493 -
Trial Evaluating the Efficacy of CARBOPLATIN in Metastatic Prostate Cancer With Gene Alterations in the Homologous Recombination Pathway
|
Phase 2 | |
Recruiting |
NCT04549207 -
Comparing Continuation or De-escalation of Bone Modifying Agents (BMA) in Patients Treated for Over 2 Years for Bone Metastases From Either Breast or Castration-resistant Prostate Cancer
|
Phase 4 | |
Active, not recruiting |
NCT03305224 -
The Combination Therapy With Ra-223 and Enzalutamide
|
Phase 2 | |
Active, not recruiting |
NCT04090528 -
pTVG-HP DNA Vaccine With or Without pTVG-AR DNA Vaccine and Pembrolizumab in Patients With Castration-Resistant, Metastatic Prostate Cancer
|
Phase 2 | |
Recruiting |
NCT04070209 -
Management of Oligoprogressive Castration Resistant Prostate Cancer (PCS X)
|
Phase 2 | |
Active, not recruiting |
NCT06193993 -
Effect of Low-dose 500 mg Abiraterone Acetate in Treatment of Metastatic Prostate Cancer Patients
|
Phase 1 | |
Completed |
NCT02669771 -
Long-Term Specified Drug Use-Results Survey for Xtandi Capsule
|
||
Active, not recruiting |
NCT05084859 -
A Study Evaluating the Safety, Pharmacokinetics, and Preliminary Efficacy of Orally Administered SM08502 Combined With Hormonal Therapy or Chemotherapy in Subjects With Advanced Solid Tumors
|
Phase 1 | |
Recruiting |
NCT03934164 -
Molecular Stratification Profiling Protocol in Metastatic Castration Resistant Prostate Cancer (mCRPC) - MAESTRO
|
||
Recruiting |
NCT03506997 -
Trial of Pembrolizumab in Metastatic Castration Resistant Prostate Cancer
|
Phase 2 | |
Completed |
NCT03569280 -
Evaluation of Safety and Efficacy of KPG-121 Plus Enzalutamide, Abiraterone or Apalutamide in CRPC Patients
|
Phase 1 | |
Enrolling by invitation |
NCT03356912 -
CABAzitaxel With or Without Prednisone in Patients With Metastatic CAstration REsistant Prostate Cancer Progressed During or After a Previous Docetaxel-based Chemotherapy
|
Phase 2 | |
Not yet recruiting |
NCT04148885 -
A Trial of Paclitaxel (Albumin-binding) for Castration-resistant Prostate Cancer
|
Phase 1/Phase 2 |