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Expression of Molecular Markers in Circulating Tumor Cells of Metastatic Castration-Resistant Prostate Cancer

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Fudan University

Status

Unknown

Conditions

Prostate Cancer Metastatic

Treatments

Other: Blood drawing

Study type

Observational

Funder types

Other

Identifiers

NCT03089099
CTC-mCRPC

Details and patient eligibility

About

As prostate cancer progresses into castration-resistant stage from initial hormone-sensitive status, the biological behavior of tumor cells that dissociated from primary lesions changed. Considered a "liquid biopsy," these circulating tumor cells (CTCs) can show how a patient's cancer responded to treatments. The purpose of this study is to determine whether sequentially analyzing the expression of molecular markers in high volume circulating tumor cells in metastatic castration-resistant prostate cancer patients can predict the therapeutic effects and outcomes of these patients.

Enrollment

100 estimated patients

Sex

Male

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Male patients
  2. 18 yrs and older, and 80 yrs and younger
  3. Histologically or cytologically proven prostate adenocarcinoma;
  4. Imaging examinations including Emission Computed Tomography (ECT), Positron Emission Tomography (PET) and so on revealed a high-volume disease of patients(A high-volume of disease was defined by the presence of visceral metastases or four or more bone lesions with at least one beyond the vertebral bodies and pelvis)
  5. Have been received hormonal therapy and progressed into castration-resistant stage
  6. Not yet receiving chemotherapy
  7. Patients are willing to participate and can be followed up regularly

Exclusion criteria

  1. Received the treatment of abiraterone acetate previously
  2. Patients received chemotherapy previously
  3. Combined with other malignant tumor history (in addition to the skin basal cell carcinoma or other tumors that have been cured more than five years).

Trial contacts and locations

1

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Central trial contact

Dai Bo, MD

Data sourced from clinicaltrials.gov

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