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PSA of 0.1 18 months after robotic prostatectomy

Answer

Generated by iatroX. Developer: Dr Kola Tytler MBBS CertHE MBA MRCGP (General Practitioner).
Last reviewed: 2 August 2025
A prostate-specific antigen (PSA) level of 0.1 ng/mL measured 18 months after robotic prostatectomy is a very low value. The clinical significance of this level primarily depends on the trend of serial PSA measurements, as biochemical relapse after radical treatment is defined by a rising PSA 1. Key considerations for this PSA level include:
  • Follow-up Schedule: After radical treatment, PSA levels should be checked no earlier than 6 weeks post-treatment, at least every 6 months for the first 2 years, and then at least once a year thereafter 1. A measurement at 18 months aligns with this recommended schedule.
  • Biochemical Relapse: Biochemical relapse is indicated by a rising PSA after radical treatment 1. While 0.1 ng/mL is low, it is crucial to compare it with previous PSA values, especially the nadir (lowest point) achieved after surgery. If this represents a rise from an undetectable level, it could signify biochemical relapse.
  • Analysis of Serial Levels: Serial PSA levels after radical treatment should be analysed using the same assay technique 1.
  • Management of Biochemical Relapse: If a rising PSA indicates biochemical relapse:
    • A rising PSA alone should not necessitate an immediate change in treatment 1.
    • Estimate the PSA doubling time, based on a minimum of 3 measurements over at least a 6-month period 1.
    • For people with biochemical relapse after radical prostatectomy and no known metastases, radical radiotherapy to the prostatic bed should be offered 1.
    • An isotope bone scan should be offered if symptoms or PSA trends suggest metastases 1.
    • Biopsy of the prostatic bed should not be offered 1.
    • Hormonal therapy should not be routinely offered unless there is symptomatic local disease progression, any proven metastases, or a PSA doubling time of less than 3 months 1.
    • Consider entry into appropriate clinical trials 1.

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