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Trial Title:
Novel Therapy Target in Metastatic Prostate Cancer
NCT ID:
NCT05577689
Condition:
Prostate Neoplasms
Conditions: Official terms:
Prostatic Neoplasms
Conditions: Keywords:
prostate cancer
multi-omics
organoid
Study type:
Observational
Overall status:
Not yet recruiting
Study design:
Time perspective:
Prospective
Intervention:
Intervention type:
Other
Intervention name:
Tissue
Description:
Tissue will be derived from patients during a standard of care procedure
Arm group label:
All patients
Summary:
The aim of this study is to use multiomics sequencing to explore the molecular
characteristics of metastatic prostate cancer (mPCa), especially metastatic
castration-resistant prostate cancer (mCRPC). At the same time, mCRPC models will be
constructed, including organoids and animal models, serving as a basic and translational
research platform to help identify novel drug targets for mPCa.
Detailed description:
Although substantial progress in treatments for prostate cancer have been made in the
past decades, distant metastasis and drug resistance remained a major cause of prostate
cancer-related deaths. The five-year survival rate for men with mPCa was only 30% and all
patients with mPCa would inevitably progress to the castration-resistant stage with
limited therapeutic chance. In China, the current situation is more worrying, with
rapidly increasing PCa incidence and higher proportion of mPCa diagnosed compared with
the Western nations (~30% vs ~5%).
Multiomics sequencing provides a promising strategy to discover the underlying molecular
basis driving metastasis and resistance and identify the new treatment strategies for
patients with mCRPC. The candidate drug target revealed by the multiomics sequencing
could be further examined in the organoid and animal models, facilitating the clinical
application from basic discovery.
This study can establish a mCRPC research system to find the molecular mechanism and
potential intervention targets of mCRPC, thereby paving the way for the discovery of new
treatments for mCRPC patients.
Criteria for eligibility:
Study pop:
Patients with metastatic prostate cancer especially metastatic castration resistant
prostate cancer will be recruited for this study.
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
1. Histologically confirmed prostate cancer
2. metastatic disease confirmed by image examination
3. Patients who can undergo surgery or biopsy for prostate cancer
4. Able to provide informed consent
Exclusion Criteria:
1. Patients diagnosed with other types of cancer besides prostate cancer
2. Not accessible to surgery sample
3. Patients fail to provide informed consent
4. Other situation that researchers think are unsuitable for this study
Gender:
Male
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Start date:
March 1, 2023
Completion date:
May 1, 2026
Lead sponsor:
Agency:
Fudan University
Agency class:
Other
Source:
Fudan University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05577689