Skip to content

To explore the selection of neoadjuvant therapy for locally advanced prostate cancer based on precision classification by RNA sequencing

To explore the selection of neoadjuvant therapy for locally advanced prostate cancer based on precision classification by RNA sequencing

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000037378
Enrollment
Unknown
Registered
2020-08-28
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-10-19

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:N/A

Sponsors

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

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1) 18-75 years old, male; 2) Confirmed prostatic adenocarcinoma by histopathology or cytology; 3) According to the Eau-Eostro-SIOG 2016 guideline, PCa was clinically diagnosed as locally progressive; 4) Had not received new endocrine therapy such as abiraterone or enzalutamide before; 5) Had not received docetaxel or cabatax or combined chemotherapy including docetaxel or cabatax in the past; 6) Had not received PARP inhibitor treatment before; 7) Had not received Xofigo(radium 223 dichloride) treatment before; 8) ECOG score 0-2; 9) Patients have signed informed consent and are capable of following planned study visits, providing blood samples before and after treatment, providing clinical information and cooperating with other study steps.

Exclusion criteria

Exclusion criteria: 1) Histopathological examination of the patient indicated neuroendocrine type/small cell prostate cancer; 2) Having hypertension and poor drug control; 3) Patients with severe cardiopulmonary insufficiency; 4) Abnormal coagulation function, bleeding tendency, or thrombolysis or anticoagulant therapy; 5) any previous diagnosis of any other malignant tumor; 6) Other malignant tumors at the same time; 7) A history of human immunodeficiency virus infection, other acquired or congenital immunodeficiency diseases, or a history of organ transplant, or a history of organ transplant; 8) The clinical information needed for the study cannot be obtained (such as loss of patient follow-up).

Design outcomes

Primary

MeasureTime frame
Time to recurrence;

Countries

China

Contacts

Public ContactZhu Yinjie

Renji Hospital, School of Medicine, Shanghai Jiaotong University

18955035798@163.com+86 18017710109

Outcome results

None listed

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