Who, When, and How: Watchful Waiting in the ERSPC Rotterdam.
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[BACKGROUND AND OBJECTIVE] Long-term data identifying which patients managed with watchful waiting (WW) ultimately require androgen deprivation therapy (ADT) are limited.
- 95% CI 26-39
APA
Jeroen Lodder, Esmée F.H. Mulder, et al. (2026). Who, When, and How: Watchful Waiting in the ERSPC Rotterdam.. European urology open science, 87, 40-47. https://doi.org/10.1016/j.euros.2026.03.013
MLA
Jeroen Lodder, et al.. "Who, When, and How: Watchful Waiting in the ERSPC Rotterdam.." European urology open science, vol. 87, 2026, pp. 40-47.
PMID
42004831 ↗
Abstract 한글 요약
[BACKGROUND AND OBJECTIVE] Long-term data identifying which patients managed with watchful waiting (WW) ultimately require androgen deprivation therapy (ADT) are limited. Using 18-yr follow-up data from the Rotterdam section of the European Randomized Study for Prostate Cancer, we examined WW practices and identified prognostic factors for ADT initiation.
[METHODS] Men whose initial management strategy was WW were included and stratified by European Association of Urology risk group. WW practices were evaluated by the frequency of follow-up visits, prostate-specific antigen (PSA) testing, and imaging. Prognostic factors for ADT initiation were identified using a Fine-Gray competing risk model and used to predict 18-yr ADT-free survival for three hypothetical patients representing the risk groups.
[KEY FINDINGS AND LIMITATIONS] We included 537 men with a median follow-up of 12.9 yr (interquartile range: 7.5-16.7). At 18 yr, cumulative incidence of ADT initiation was 6.6% (95% confidence interval [CI]: 0.02-13), 33% (95% CI 26-39), and 55% (95% CI 47-64) in men at low, intermediate, and high risk, respectively. Most patients received regular follow-up every 6 mo, regardless of risk group, whereas imaging was uncommon except in men at higher risk. PSA, grade group, and clinical T-stage were statistically significant predictors of ADT initiation. Predicted 18-yr ADT-free survival ranged from 90% in men at low risk to 35% in men at high risk. Limitations include the retrospective design, use of ADT initiation as an end point without standardized triggers, and a historical cohort, possibly affecting internal validity and generalizability.
[CONCLUSIONS AND CLINICAL IMPLICATIONS] Follow-up for men managed with WW could be individualized based on patient and tumor characteristics to reduce unnecessary visits while preserving timely detection of progression.
[METHODS] Men whose initial management strategy was WW were included and stratified by European Association of Urology risk group. WW practices were evaluated by the frequency of follow-up visits, prostate-specific antigen (PSA) testing, and imaging. Prognostic factors for ADT initiation were identified using a Fine-Gray competing risk model and used to predict 18-yr ADT-free survival for three hypothetical patients representing the risk groups.
[KEY FINDINGS AND LIMITATIONS] We included 537 men with a median follow-up of 12.9 yr (interquartile range: 7.5-16.7). At 18 yr, cumulative incidence of ADT initiation was 6.6% (95% confidence interval [CI]: 0.02-13), 33% (95% CI 26-39), and 55% (95% CI 47-64) in men at low, intermediate, and high risk, respectively. Most patients received regular follow-up every 6 mo, regardless of risk group, whereas imaging was uncommon except in men at higher risk. PSA, grade group, and clinical T-stage were statistically significant predictors of ADT initiation. Predicted 18-yr ADT-free survival ranged from 90% in men at low risk to 35% in men at high risk. Limitations include the retrospective design, use of ADT initiation as an end point without standardized triggers, and a historical cohort, possibly affecting internal validity and generalizability.
[CONCLUSIONS AND CLINICAL IMPLICATIONS] Follow-up for men managed with WW could be individualized based on patient and tumor characteristics to reduce unnecessary visits while preserving timely detection of progression.
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