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NCT03789253Recruiting

Identify Genes/Pathways Responsible for Progression From Low Risk to Higher Risk Prostate Cancer

Identify Genes/Pathways Responsible for Progression From Low Risk to Higher Risk Prostate Cancer-A New Strategy for Prostate Cancer Prevention

Source: ClinicalTrials.gov · Last updated 12 Aug 2022 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

In Taiwan, about 70% of new incident prostate cancer patients have localized disease. Most patients were detected by PSA screening. Among them, many had low-risk PC, which is very likely latent in nature, progresses slowly, and rarely leads to death. Most patients died of other causes, such as other cancers, cardiovascular diseases, and diabetes mellitus. Many guidelines recommend that active surveillance (AS) or watchful waiting (WW) is a good option for low risk patients to avoid overtreatment-related complications. However, 30% of patients on AS will finally need definitive treatments due to disease progression within 10 years. We hypothesize that there are differential gene expressions between progressive and non-progressive tumors. If we can identify key genes or pathways that are responsible for progression of low risk PC to higher risk diseases, PC progression could be reduced substantially by regulating these genes or pathways and maintain long-term cancer latency to control non-metastatic PC. In light of the high prevalence rate of latent PC in adult men, the strategy is in fact the best strategy for preventing clinical PC.

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
26 Dec 2018
Start date
2 Jan 2019
Primary completion date
31 Jul 2030
Lead sponsor
National Taiwan University Hospital
NCT number
NCT03789253

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 2 Jan 2019 to the primary completion date, 31 Jul 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Have received systemic chemotherapy, pelvic radiotherapy or androgen deprivation therapy (ADT) before the obtainment of pathological specimen from prostate operation or biopsy.

Other

  • Subjects who disagree with signing the informed consent.

Who the study is looking for

  • Historically or cytologically confirmed adenocarcinoma of prostate.
  • Have or ever received active Surveillance as the main conservative management at NTUH (National Taiwan University Hospital).
  • Have or will receive prostate biopsy to confirm tumor progression after the diagnosis of prostate cancer.

Age in the registry: 40 years to 100 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Taiwan University
Coordinator of this site? Confirm its status
TaipeiTaiwanRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.