2020
DOI: 10.1007/s10147-020-01676-z
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External validation of the "optimal PSA follow-up schedule after radical prostatectomy” in a new cohort

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Cited by 6 publications
(12 citation statements)
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“…Patients with pN1-or pT3b-status were excluded in the study of Swanson et al Other studies showed that patients with pN1 or pT3b had an even higher risk of CSM and should definitely be monitored [17]. Matsumoto et al analyzed the optimal follow-up scheme in patients after RARP based on the PSA-doubling time with the aim to find every single BCR before it exceeds 0.4 ng/mL [18,19]. Their optimal schedule was, for the most part in line with the EAU guidelines, every 3 months for the first year, every 4 months the second year and semiannually thereafter [3].…”
Section: Discussionmentioning
confidence: 99%
“…Patients with pN1-or pT3b-status were excluded in the study of Swanson et al Other studies showed that patients with pN1 or pT3b had an even higher risk of CSM and should definitely be monitored [17]. Matsumoto et al analyzed the optimal follow-up scheme in patients after RARP based on the PSA-doubling time with the aim to find every single BCR before it exceeds 0.4 ng/mL [18,19]. Their optimal schedule was, for the most part in line with the EAU guidelines, every 3 months for the first year, every 4 months the second year and semiannually thereafter [3].…”
Section: Discussionmentioning
confidence: 99%
“…Patients with pN1- or pT3b-status were excluded in the study of Swanson et al Other studies showed that patients with pN1 or pT3b had an even higher risk of CSM and should definitely be monitored [ 17 ]. Matsumoto et al analyzed the optimal follow-up scheme in patients after RARP based on the PSA-doubling time with the aim to find every single BCR before it exceeds 0.4 ng/mL [ 18 , 19 ]. Their optimal schedule was, for the most part, in line with the EAU guidelines, every 3 months for the first year, every 4 months for the second year, and semiannually thereafter [ 3 ].…”
Section: Discussionmentioning
confidence: 99%
“…We considered the ideal PSA range for the detection of BCR to be 0.2-0.4 ng/ mL, at which we can start salvage treatment before the PSA level exceeds 0.5 ng/mL [4]. In our previous studies [8][9][10], we calculated the PSA-DT in patients who underwent RP between 1995 and 2017 and experienced BCR. The majority of the cohort did not undergo NHT.…”
Section: Discussionmentioning
confidence: 99%
“…Patients should be followed up closely during the early phase after RP when aggressive disease recurrence can develop. The risk of rapid BCR gradually decreases over time and the follow-up frequency can be reduced in the late phase [8][9][10].…”
Section: Introductionmentioning
confidence: 99%