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Personalized schedules for surveillance of low‐risk prostate cancer patients

Author

Listed:
  • Anirudh Tomer
  • Daan Nieboer
  • Monique J. Roobol
  • Ewout W. Steyerberg
  • Dimitris Rizopoulos

Abstract

Low‐risk prostate cancer patients enrolled in active surveillance (AS) programs commonly undergo biopsies on a frequent basis for examination of cancer progression. AS programs employ a fixed schedule of biopsies for all patients. Such fixed and frequent schedules may schedule unnecessary biopsies. Since biopsies are burdensome, patients do not always comply with the schedule, which increases the risk of delayed detection of cancer progression. Motivated by the world's largest AS program, Prostate Cancer Research International Active Surveillance (PRIAS), we present personalized schedules for biopsies to counter these problems. Using joint models for time‐to‐event and longitudinal data, our methods combine information from historical prostate‐specific antigen levels and repeat biopsy results of a patient, to schedule the next biopsy. We also present methods to compare personalized schedules with existing biopsy schedules.

Suggested Citation

  • Anirudh Tomer & Daan Nieboer & Monique J. Roobol & Ewout W. Steyerberg & Dimitris Rizopoulos, 2019. "Personalized schedules for surveillance of low‐risk prostate cancer patients," Biometrics, The International Biometric Society, vol. 75(1), pages 153-162, March.
    • Handle: RePEc:bla:biomet:v:75:y:2019:i:1:p:153-162
    DOI: 10.1111/biom.12940
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    References listed on IDEAS

    as
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