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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04126915
Other study ID # mCRPC-WES2019
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date November 8, 2019
Est. completion date October 8, 2024

Study information

Verified date October 2019
Source Changhai Hospital
Contact jing li, PHD
Phone +81-15801966205
Email drlijing@163.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Through gene sequencing of the patient's tissue, to figure out the genomic characteristics of patients with advanced disease and guide the treatment of patients


Description:

Tumor heterogeneity and tumor clonal evolution cause he diagnosis and treatment difficulties of advanced prostate cancer. Heterogeneity exists in different lesions at the same location of the same tumor, between lesions at different locations, and in the same lesion in different processes of disease progression. Tumor heterogeneity causes different tumor patients to respond differently to different treatments; as patients progress, tumor patients gradually develop clonal evolution, and the original effective treatment will lose the therapeutic effect. And routine imaging examinations and PSA examinations are also difficult to respond to changes in the patient's condition in a timely manner. By Genetic testing of the primary tumor, metastases or blood of the patient, and according to the test result of the patient, the patient's medication treatment can be provided, and the patient's condition change can be monitored. Studies have shown that patients with different mutation types respond differently to the same treatment. Prostate cancer patients with AR-V7 mutations have a poorer response to abiraterone or dextrozamide than patients with prostate cancer without AR-V7 mutation; whereas for solid tumors with MSI-H or dMMR, PD-1 Inhibitors can also bring the desired results to such patients. Therefore, according to the genetic test results of the patient's tumor tissue, early diagnosis can also be given, and the patient's condition change and precise treatment can be predicted.In this study, the investigators hope to obtain the genome characteristics of advanced patients by performing whole exon sequencing on the patient's tissues, and to guide the patients' follow-up treatment through sequencing results, to observe the effects of different treatment methods on patients and find biomarker that predict patient prognosis


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date October 8, 2024
Est. primary completion date October 8, 2022
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Expected survival period = half a year;

- Whole body bone scan (ECT) and magnetic resonance imaging (MRI) or PET-CT are evaluated as metastatic castration to resist prostate cancer patients;

- Patients with evaluable and retrievable lesions;

- Patients who voluntarily receive the experimental study protocol after informing the existing treatment plan;

Exclusion Criteria:

- Patients with other malignancies, or in acute infection or other severe infections; immunodeficiency virus (HIV), hepatitis C virus (HCV) and/or syphilis-positive patients;

- Patients who have long-term anticoagulant and anti-platelet aggregation drugs (the anticoagulant is discontinued for less than 1 week);

- At the same time suffering from other serious systemic diseases, the researchers believe that it may interfere with the treatment, evaluation and compliance of this test, including severe respiratory, circulatory, neurological, mental, digestive, endocrine, immune, urinary and other systems. disease;

- The patient that it is inappropriate to participate in this clinical trial

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
Whole Exome Sequencing
Whole Exome Sequencing of the patient's primary tumor, metastases

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Yinghao Sun

Outcome

Type Measure Description Time frame Safety issue
Primary The genetic characteristics of mCRPC patients in China The genetic characteristics of mCRPC patients in China as Assessed by Gene Sequencing June 2020
Secondary the possible prognostic therapeutic target the possible prognostic therapeutic target as Assessed by Gene Sequencing ,by observing the patient's prognosis,including PSA progression and progression in imaging by RECIST Version 1.1 June 2023
Secondary The best method to treat the disease Compare the effects of different treatments on the prognosis of patients as Assessed by PSA progression and progression in imaging by RECIST Version 1.1 June 2023
See also
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Completed NCT02398526 - Pain Evaluation in Radium-223 Treated Castration Resistant Prostate Cancer Patients With Bone Metastases
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Terminated NCT04404140 - A Study Evaluating The Safety, Efficacy and Pharmacokinetics Of Ipatasertib In Combination With Atezolizumab And Docetaxel In Metastatic Castration-Resistant Prostate Cancer (mCRPC). Phase 1
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Active, not recruiting NCT03748641 - A Study of Niraparib in Combination With Abiraterone Acetate and Prednisone Versus Abiraterone Acetate and Prednisone for Treatment of Participants With Metastatic Prostate Cancer Phase 3
Recruiting NCT05293496 - A Study of MGC018 in Combination With MGD019 in Participants With Advanced Solid Tumors Phase 1
Available NCT06033001 - Expanded Access Treatment With [Lu-177]-PNT2002 for Adult Patients With Prostate-Specific Membrane Antigen (PSMA)-Positive Metastatic Castration-Resistant Prostate Cancer (mCRPC)