← TrialMatch
HomeTrials

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

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, cardiovasc

Condition(s)Prostate Cancer Stage I
StatusRecruiting
Study typeObservational
SummaryIn 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 res
Who can participateInclusion Criteria: 1. Historically or cytologically confirmed adenocarcinoma of prostate. 2. Have or ever received active Surveillance as the main conservative management at NTUH (National Taiwan University Hospital). 3. Have or will receive prostate biopsy to confirm tumor progression after the diagnosis of prostate cancer. Exclusion Criteria: 1. Have received systemic chemotherapy, pelvic radiotherapy or androgen deprivation therapy (ADT) before the obtainment of pathological specimen from prostate operation or biopsy. 2. Subjects who disagree with signing the informed consent.
Ages40 Years to 100 Years
SexMale
Lead sponsorNational Taiwan University Hospital
LocationsTaipei, Taiwan
Start date2019-01-02
NCT IDNCT03789253
Official listinghttps://clinicaltrials.gov/study/NCT03789253

🔍 Search all trials →