Outcomes of active surveillance for clinically localized prostate cancer in a middle eastern tertiary care center


Submitted: May 14, 2021
Accepted: July 19, 2021
Published: December 20, 2021
Abstract Views: 1067
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Authors

  • Mohammad Hout Department of Surgery, Division of Urology, American University of Beirut Medical Center, Beirut, Lebanon.
  • Ali Merhe Department of Surgery, Division of Urology, American University of Beirut Medical Center, Beirut, Lebanon.
  • Nassib Abou Heidar Department of Surgery, Division of Urology, American University of Beirut Medical Center, Beirut, Lebanon.
  • Jose M. El-Asmar Department of Surgery, Division of Urology, American University of Beirut Medical Center, Beirut, Lebanon.
  • Wassim Wazzan Department of Surgery, Division of Urology, American University of Beirut Medical Center, Beirut, Lebanon.
  • Bassel Bachir Department of Surgery, Division of Urology, American University of Beirut Medical Center, Beirut, Lebanon.
  • Rola Jaafar Department of Surgery, American University of Beirut Medical Center, Beirut, Lebanon.
  • Albert El-Hajj Division of Urology, Department of Surgery, American University of Beirut Medical Center, Beirut, Lebanon, Lebanon.
  • Muhammad Bulbul Department of Surgery, Division of Urology, American University of Beirut Medical Center, Beirut, Lebanon.

Background: The aim of our study was to evaluate the outcome of active surveillance (AS) for prostate cancer for a cohort of patients at our institution.
Methods: A total of 43 patients with low risk prostate cancer were enrolled in an active surveillance pilot program at our institution between 2008 and 2018. Follow up protocols included: periodic prostate specific antigen (PSA), digital rectal examination (DRE), multiparametric MRI, and prostate biopsy at one year. Pertinent parameters were collected, and descriptive statistics were reported along with a subset analysis of patients that dropped out of the protocol to receive active treatment for disease progression.
Results: Out of 43 eligible patients, 46.5% had a significant rise in follow up PSA. DRE was initially suspicious in 27.9% of patients, and none had any change in DRE on follow up. Initially, prostate MRIs showed PIRADS 3, 4, and 5 in 14%, 37.2%, and 11.6% respectively, while 23.2% had a negative initial MRI. 14% did not have an MRI. Upon follow up, 18.6% of patients had progression on MRI. Initial biopsies revealed that 86% were classified as WHO group 1, while 14% as WHO group 2. With regards to the follow up biopsies, 11.6% were upgraded. 20.9% of our patients had active treatment; 44.4% due to upgraded biopsy results, 22.2% due to PSA progression, 22.2% due to strong patient preference, and 11.1% due to radiologic progression.
Conclusions: For selected men with low risk prostate cancer, AS is a reasonable alternative. The decision for active treatment should be tailored upon changes in PSA, DRE, MRI, and biopsy results.


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Hout, M., Merhe, A., Heidar, N. A., El-Asmar, J. M., Wazzan, W., Bachir, B., Jaafar, R., El-Hajj, A., & Bulbul, M. (2021). Outcomes of active surveillance for clinically localized prostate cancer in a middle eastern tertiary care center. Archivio Italiano Di Urologia E Andrologia, 93(4), 385–388. https://doi.org/10.4081/aiua.2021.4.385

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