Magnetic Resonance Imaging at Second Surveillance Biopsy After Diagnosis in Patients With Grade Group 1 Prostate Cancer in the Canary Prostate Active Surveillance Study.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: vs without prior MRI-informed biopsy
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSIONS] These results support MRI use at Biopsy 2 and suggest negative surveillance MRI should not replace Biopsy 2. Both targeted and systematic cores should be taken at Biopsy 2 in patients with and without prior MRI on active surveillance.
[PURPOSE] No clear guidelines exist regarding MRI use after confirmatory biopsy during active surveillance.
- 표본수 (n) 101
APA
Chappidi MR, Newcomb LF, et al. (2025). Magnetic Resonance Imaging at Second Surveillance Biopsy After Diagnosis in Patients With Grade Group 1 Prostate Cancer in the Canary Prostate Active Surveillance Study.. The Journal of urology, 214(3), 251-258. https://doi.org/10.1097/JU.0000000000004592
MLA
Chappidi MR, et al.. "Magnetic Resonance Imaging at Second Surveillance Biopsy After Diagnosis in Patients With Grade Group 1 Prostate Cancer in the Canary Prostate Active Surveillance Study.." The Journal of urology, vol. 214, no. 3, 2025, pp. 251-258.
PMID
40305682 ↗
Abstract 한글 요약
[PURPOSE] No clear guidelines exist regarding MRI use after confirmatory biopsy during active surveillance. Our objective was to evaluate MRI performance after confirmatory biopsy in patients with vs without prior MRI-informed biopsy.
[MATERIALS AND METHODS] Patients in the Canary Prostate Active Surveillance Study with Gleason Grade Group (GG) 1 disease undergoing MRI-informed Biopsy 2, defined as second surveillance biopsy after diagnosis, were separated into prior vs no prior MRI-informed biopsy groups. Primary outcome was reclassification (≥GG2) at MRI-informed Biopsy 2. Reclassification rates and location (systematic cores, targeted cores, both) were compared between groups. Univariable and multivariable logistic regression identified predictors of reclassification.
[RESULTS] Patients with (n = 101) vs without (n = 103) prior MRI-informed biopsy had lower reclassification rates at Biopsy 2 (21% vs 36%, = .017) and lower GG at reclassification (95% vs 73% of reclassifications to GG2, = .039). In multivariable modeling, Prostate Imaging Reporting and Data System 4 or 5 lesion at MRI-informed Biopsy 2 was associated with increased odds of reclassification (odds ratio = 2.04, 95% CI [1.04-4.05]). The negative predictive value of MRI at Biopsy 2 was 87% (95% CI [78-96]) and 73% (95% CI [61-85]) in with vs without prior MRI groups. Reclassification location was identified by targeted cores only in 36% vs 19% of patients with vs without prior MRI ( = .4). Reclassification location was identified by systematic cores only in 36% vs 58% of patients with vs without prior MRI ( = .4).
[CONCLUSIONS] These results support MRI use at Biopsy 2 and suggest negative surveillance MRI should not replace Biopsy 2. Both targeted and systematic cores should be taken at Biopsy 2 in patients with and without prior MRI on active surveillance.
[MATERIALS AND METHODS] Patients in the Canary Prostate Active Surveillance Study with Gleason Grade Group (GG) 1 disease undergoing MRI-informed Biopsy 2, defined as second surveillance biopsy after diagnosis, were separated into prior vs no prior MRI-informed biopsy groups. Primary outcome was reclassification (≥GG2) at MRI-informed Biopsy 2. Reclassification rates and location (systematic cores, targeted cores, both) were compared between groups. Univariable and multivariable logistic regression identified predictors of reclassification.
[RESULTS] Patients with (n = 101) vs without (n = 103) prior MRI-informed biopsy had lower reclassification rates at Biopsy 2 (21% vs 36%, = .017) and lower GG at reclassification (95% vs 73% of reclassifications to GG2, = .039). In multivariable modeling, Prostate Imaging Reporting and Data System 4 or 5 lesion at MRI-informed Biopsy 2 was associated with increased odds of reclassification (odds ratio = 2.04, 95% CI [1.04-4.05]). The negative predictive value of MRI at Biopsy 2 was 87% (95% CI [78-96]) and 73% (95% CI [61-85]) in with vs without prior MRI groups. Reclassification location was identified by targeted cores only in 36% vs 19% of patients with vs without prior MRI ( = .4). Reclassification location was identified by systematic cores only in 36% vs 58% of patients with vs without prior MRI ( = .4).
[CONCLUSIONS] These results support MRI use at Biopsy 2 and suggest negative surveillance MRI should not replace Biopsy 2. Both targeted and systematic cores should be taken at Biopsy 2 in patients with and without prior MRI on active surveillance.
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