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The application of targeted gene sequencing in predicting the prognosis of metastatic castration resistant prostate cancer

The application of targeted gene sequencing in predicting the prognosis of metastatic castration resistant prostate cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000037036
Enrollment
Unknown
Registered
2020-08-26
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-28

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

Conditions

Prostate cancer

Interventions

case series:abiraterone

Sponsors

Renji Hospital affiliated to Shanghai Jiaotong University, School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: a) The age was 18-75 years old, male; b) Prostate adenocarcinoma was diagnosed by histopathology or cytology; c) According to eau-estro-siog 2016 guidelines, the clinical diagnosis was metastatic castration resistant prostate cancer; d) Had not received novel hormonal therapy such as abiraterone and enzalutamide; e) Had not received docetaxel or carbataxel or combination chemotherapy including docetaxel or carbataxel in the past; f) No previous treatment with PARP inhibitors; g) Had never received xofigo (radium 223 dichloride) treatment before; h) ECOG score was 0-2; i) The patients had normal organ function, WBC >= 3000 / mm3 or neutrophil count >= 1500 / mm3, AST and ALT were lower than 1.5 ULN; j) The survival time of the patients was expected to be more than 3 months; k) Patients sign informed consent and have the ability to follow the planned study visit, provide blood samples before and after treatment, provide clinical information and cooperate with other research steps.

Exclusion criteria

Exclusion criteria: a) Histopathological examination showed neuroendocrine / small cell prostate cancer; b) Hypertension and poor drug control; c) Patients with severe cardiopulmonary insufficiency; d) Abnormal coagulation function, bleeding tendency, or receiving thrombolytic or anticoagulant therapy; e) Any other malignant tumor previously diagnosed; f) There were other malignant tumors at the same time; g) Have a history of human immunodeficiency virus infection, or other acquired or congenital immunodeficiency diseases, or have a history of organ transplantation, or have a history of organ transplantation; h) Unable to obtain clinical information needed for the study (e.g. loss of follow-up).

Design outcomes

Primary

MeasureTime frame
PFS;PSA;

Countries

China

Contacts

Public ContactDong Baijun

Renji Hospital affiliated to Shanghai Jiaotong University, School of Medicine

dongbaijun@renji.com+86 13761210771

Outcome results

None listed

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