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Evaluation of the Metastasis and Recurrence of Prostate Cancer

Shanghai Jiao Tong University logo

Shanghai Jiao Tong University

Status

Unknown

Conditions

Prostate Cancer Recurrent
Prostate Cancer Stage
Prostate Cancer Metastatic
Prostate Cancer (Diagnosis)

Study type

Observational

Funder types

Other

Identifiers

NCT03507595
XH-17-020

Details and patient eligibility

About

This study aims to use the new molecular probe 18F-PSMA for the diagnosis,staging ,recurrence monitoring and evaluation of the prostate cancer.By compared with the conventional imaging methods (whole body bone scintigraphy and MRI) and molecular imaging methods (11C-choline PET/CT),we hope to find the advantages of 18F-PSMA PET/CT in the diagnosis and metastases of prostate cancer, and lay the foundation for the further clinical transformation.

Full description

This study aims to use the new molecular probe 18F-PSMA for the diagnosis,staging ,recurrence monitoring and evaluation of the prostate cancer.By compared with the conventional imaging methods (whole body bone scintigraphy and MRI) and molecular imaging methods (11C-choline PET/CT),we hope to find the advantages of 18F-PSMA PET/CT in the diagnosis and metastases of prostate cancer, and lay the foundation for the further clinical transformation.And make some comparison with those 3 methods.

Enrollment

400 estimated patients

Sex

Male

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients with initial diagnosis of prostate cancer; 1)T2 stage: PSA>20ng/ml, Gleason Score >= 8; 2)T3 or T4 stage; 3)The imaging examination was negative or localized metastasis of the pelvic lymph node, but there was no distant metastasis of lymph nodes or bone and internal organs other than the pelvic cavity.
  2. Patients with biochemical recurrent prostate cancer; 1)After the RRP surgery, the serum PSA was over 0.2 ng/ml in two consecutive sera; 2)After the radiotherapy: the lowest PSA is up to 2 ng/ml.
  3. Patients with CRPC. 1)The serum testosterone is in the castration level (< 50 ng/dL or < 1.7 nmol/L); 2)The PSA is elevated 3 times in a row, the base value is increased by more than 50%, and the PSA > 2ng/mL(the interval is one week); 3)The continuation of the anti-androgen drugs, flunamine was stopped for at least 4 weeks, and biglumide was suspended for at least 6 weeks; 4)Despite the continued standard androgen deprivation therapy, the PSA is still progressing.

Exclusion criteria

  1. Patients who are unwilling to participate in the study or unwilling to sign the informed consent forms;
  2. Patients who are critically ill, suffering from mental illness and cannot cooperate with the examination;
  3. There are electronic implants, such as pacemakers and insulin pumps in the body, and magnetic metal foreign objects in the spot.

Trial design

400 participants in 3 patient groups

Patients with initial diagnosis of PCa
Description:
1. T2 stage: PSA\>20ng/ml, Gleason Score \>= 8; 2. T3 or T4 stage; 3. The imaging examination was negative or localized metastasis of the pelvic lymph node, but there was no distant metastasis of lymph nodes or bone and internal organs other than the pelvic cavity.
Patients with biochemical recurrent PCa
Description:
1. After the RRP surgery,the serum PSA was over 0.2 ng/ml in two consecutive sera; 2. After the radiotherapy: the lowest PSA is up to 2 ng/ml.
Patients with CRPC
Description:
1. The serum testosterone is in the castration level (\< 50 ng/dL or \< 1.7 nmol/L); 2. The PSA is elevated 3 times in a row, the base value is increased by more than 50%, and the PSA \> 2ng/mL(the interval is one week); 3. The continuation of the anti-androgen drugs, flunamine was stopped for at least 4 weeks, and biglumide was suspended for at least 6 weeks; 4. Despite the continued standard androgen deprivation therapy, the PSA is still progressing.

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Jun Qi, MD; Hui Wang, MD

Data sourced from clinicaltrials.gov

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