Skip to content

Study on the genetic characteristics of newly-onset and highly aggressive prostate cancer

Study on the genetic characteristics of newly-onset and highly aggressive prostate cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100046276
Enrollment
Unknown
Registered
2021-05-12
Start date
2021-05-06
Completion date
Unknown
Last updated
2021-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate cancer

Interventions

Highly aggressive prostate cancer group :Nil
Non highly aggressive prostate cancer group :Nil

Sponsors

Department of Urology, Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients in the highly aggressive group must meet one of the following conditions: (1)Prostate cancer patients with clear lymph node metastasis from imaging studies; (2)Patients with bone metastasis or distant metastasis of prostate cancer have been suggested by imaging; (3)Prostate cancer patients whose clinical stage reaches or exceeds T3b or whose postoperative pathological stage reaches or exceeds pT3b; (4)Prostate cancer patients with pathological Gleason score greater than or equal to 9 in prostate biopsy or radical resection. 2. General prostate cancer group (non-highly aggressive group): other patients undergoing radical prostatectomy. 3. Patients who can collect peripheral blood samples, if the patient has children, can also collect peripheral blood samples of their children, regardless of whether they have children, and can cooperate with the detailed family history investigation, for patients with genitourinary system tumors or breast glands in the family members of the patients Collect peripheral blood samples for cancer patients; 4. The subject reads and fully understands the patient instructions, and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who have received bone marrow transplantation; 2. Suffer from other serious systemic diseases at the same time, which the investigator thinks may interfere with the treatment, evaluation and compliance of this test, including severe breathing, circulation, nerve, spirit, digestion, endocrine, immunity, urinary, etc. Systemic disease; 3. Patients judged by the investigator to be unsuitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Whole exome sequencing in highly aggressive prostate cancer group;Whole exome sequencing in non-highly aggressive prostate cancer group;Positive rate of incision margin, no recurrence time of Biochemistry after operation, urine control after operation, recovery rate of sexual function after operation, quality of life scale, survival time, endocrine adverse reactions;Clinical and pathological information;

Countries

China

Contacts

Public ContactRen Shancheng

Department of Urology, Shanghai Changhai Hospital

renshancheng@gmail.com+86 13917793885

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026