NTTPro: Novel Therapy Target in Metastatic Prostate Cancer

Sponsor
Fudan University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05577689
Collaborator
(none)
100
38

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: Tissue

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Combining Multi-omics Analysis and Organoid Models to Search for Novel Therapy Target in Metastatic Prostate Cancer
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Nov 1, 2025
Anticipated Study Completion Date :
May 1, 2026

Arms and Interventions

Arm Intervention/Treatment
All patients

There is only one arm in the trial

Other: Tissue
Tissue will be derived from patients during a standard of care procedure

Outcome Measures

Primary Outcome Measures

  1. Multiple omics features [3 years]

    Multi-omics information including genetic profiling results, transcriptional profiling results and epigenomic profiling results will be collected and analyzed.

  2. Organoids successfully generated from metastatic prostate cancer [3 years]

    Successful isolation of prostate cancer organoids from surgical specimens of patients diagnosed with metastatic prostate cancer. We will calculate the culture efficiency and total number of organoids generated in our center.

  3. Developing of biomarkers related to cancer metastasis and drug resistant [3 years]

    To search for biomarkers related to tumor metastasis and resistance by performing multi-omics analysis to surgery specimens derived from patients with metastatic prostate cancer.

Secondary Outcome Measures

  1. Animal models successfully generated from patient derived prostate cancer organoids [3 years]

    Prostate cancer organoids with clarified characteristics will be transplanted into mice to establish PDOX models.

  2. Response of the prostate cancer organoids to the selected anti-cancer compounds [3 years]

    Organoid that are successfully cultured and characteristic clarified will be treated with the selected compounds to test their anti-cancer activity.

  3. Response of the PDOX models to the selected anti-cancer compounds [3 years]

    PDOX models that successfully established will be treated with the selected compounds to test their anti-cancer activity.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Fudan University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ding-Wei Ye, Fudan University Shanghai Cancer Center, Fudan University
ClinicalTrials.gov Identifier:
NCT05577689
Other Study ID Numbers:
  • PCa-Organoid
First Posted:
Oct 13, 2022
Last Update Posted:
Oct 13, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Keywords provided by Ding-Wei Ye, Fudan University Shanghai Cancer Center, Fudan University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 13, 2022