Long-term outcomes of active surveillance for clinically localized prostate cancer in a community-based setting: results from a prospective non-interventional study - Scorecard - MDSpire

Long-term outcomes of active surveillance for clinically localized prostate cancer in a community-based setting: results from a prospective non-interventional study

  • By

  • Jan Herden

  • Andreas Schwarte

  • Thorsten Werner

  • Uwe Behrendt

  • Axel Heidenreich

  • Lothar Weissbach

  • September 30, 2020

  • 0 min

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Clinical Scorecard: Long-term Effects of Active Surveillance on Clinically Localized Prostate Cancer in a Community Setting: Findings from a Prospective Non-Interventional Study

At a Glance

CategoryDetail
ConditionClinically localized prostate cancer (PCa)
Key MechanismsActive surveillance (AS) involves regular PSA assessment, digital rectal examination (DRE), and re-biopsies to monitor disease progression and switch to invasive treatment if needed
Target PopulationPatients with well-differentiated, localized prostate cancer (T-category ≤ cT2c, PSA ≤ 10 ng/ml, Gleason grade group 1, PSA-density ≤ 0.2 ng/ml2, ≤ 2 positive biopsies)
Care SettingCommunity setting, primarily office-based urologists

Key Highlights

  • 10-year cancer-specific survival with AS exceeds 98%, comparable to immediate invasive treatment
  • In a community setting, 56.8% of patients discontinued AS for invasive treatment over median 7.7 years follow-up
  • 10-year overall survival was 86% and metastasis-free survival was 97% in the AS cohort

Guideline-Based Recommendations

Diagnosis

  • Inclusion criteria for AS: T-category ≤ cT2c, PSA ≤ 10 ng/ml, Gleason grade group 1, PSA-density ≤ 0.2 ng/ml2, ≤ 2 positive biopsies
  • Baseline assessment includes PSA, DRE, and prostate biopsy

Management

  • Follow-up with PSA, DRE, and PSA doubling time every 3 months for first 2 years, then every 6 months
  • Re-biopsy recommended after 1 year and every 3 years thereafter
  • Discontinue AS upon histological progression, PSA-DT < 3 years, clinical progression on DRE, or patient preference

Monitoring & Follow-up

  • Regular PSA testing and DRE to detect progression
  • Repeat biopsies to assess histological changes
  • Monitor PSA doubling time as a marker of progression

Risks

  • Risk of progression requiring invasive treatment exists; 56.8% discontinued AS in this study
  • Small risk of metastasis (2.1% developed metastasis over median 7.7 years)
  • Potential for patient drop-out or loss to follow-up (20.7% in this study)

Patient & Prescribing Data

329 patients with localized prostate cancer under AS in a community setting

Over median 7.7 years, 56.8% discontinued AS for invasive treatments (radical prostatectomy, radiotherapy, hormone therapy); main reasons included biopsy upgrade and PSA elevation

Clinical Best Practices

  • Strict adherence to inclusion criteria for AS to select appropriate candidates
  • Implement structured follow-up protocols with frequent PSA, DRE, and scheduled re-biopsies
  • Promptly discontinue AS upon evidence of progression or patient preference
  • Engage patients in shared decision-making and ensure close monitoring to minimize loss to follow-up
  • Recognize that AS in community settings can achieve outcomes comparable to academic centers

References

Original Source(s)

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