Clinical outcomes for men with positive surgical margins after radical prostatectomydresults from the South Australian Prostate Cancer Clinical Outcomes Collaborative community-based registry

被引:5
作者
Beckmann, Kerri R. [1 ,2 ]
O'Callaghan, Michael E. [3 ]
Vincent, Andrew D. [4 ]
Moretti, Kim L. [1 ,3 ,5 ]
Brook, Nicholas R. [6 ]
机构
[1] Univ South Australia, Canc Epidemiol & Populat Hlth Res, Adelaide, Australia
[2] Kings Coll London, Div Pharmaceut & Canc Studies, Translat Oncol & Urol Res, London, England
[3] Flinders Med Ctr, South Australian Prostate Canc Clin Outcomes Colla, Adelaide, Australia
[4] Univ Adelaide, Adelaide Med Sch, Freemasons Fdn Ctr Mens Hlth, Adelaide, Australia
[5] Univ Adelaide, Discipline Surg, Adelaide, Australia
[6] Royal Adelaide Hosp, Dept Urol, Adelaide, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Prostate cancer; Positive surgical margin; Biochemical recurrence; Radical; prostatectomy; Outcome; BIOCHEMICAL RECURRENCE; LEARNING-CURVE; SALVAGE-RADIOTHERAPY; FROZEN-SECTION; IMPACT; SURGEON; PREDICTOR; ADJUVANT; EXPERIENCE; LOCATION;
D O I
10.1016/j.ajur.2022.02.014
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective: Positive surgical margins (PSMs) after radical prostatectomy (RP) indicate failure of surgery to completely clear cancer. PSMs confer an increased risk of biochemical recurrence (BCR), but how more robust outcomes are affected is unclear. This study investigated factors associated with PSMs following RP and determined their impact on clinical outcomes (BCR, second treatment [radiotherapy and/or androgen deprivation therapy], and prostate cancer-specific mortality [PCSM]). Methods: The study cohort included men diagnosed with prostate cancer (pT2-3b/N0/M0) be-tween January 1998 and June 2016 who underwent RP from the South Australian Prostate Cancer Clinical Outcomes Collaborative database. Factors associated with risk of PSMs were identified using Poisson regression. The impact of PSMs on clinical outcomes (BCR, second treatment, and PCSM) was assessed using competing risk regression. Results: Of the 2827 eligible participants, 28% had PSMs-10% apical, 6% bladder neck, 17% posterolateral, and 5% at multiple locations. Median follow-up was 9.6 years with 81 deaths from prostate cancer recorded. Likelihood of PSM increased with higher pathological grade and pathological tumor stage, and greater tumour volume, but decreased with increasing sur-geon volume (odds ratio [OR]: 0.93; 95% confidence interval [CI]: 0.88-0.98, per 100 previous prostatectomies). PSMs were associated with increased risk of BCR (adjusted sub-distribution hazard ratio [sHR] 2.5; 95% CI 2.1-3.1) and second treatment (sHR 2.9; 95% CI 2.4-3.5). Risk of BCR was increased similarly for each PSM location, but was higher for multiple margin sites. We found no association between PSMs and PCSM. Conclusion: Our findings support previous research suggesting that PSMs are not independently associated with PCSM despite strong association with BCR. Reducing PSM rates remains an important objective, given the higher likelihood of secondary treatment with associated co -morbidities. 2023 Editorial Office of Asian Journal of Urology. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
引用
收藏
页码:502 / 511
页数:10
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