A proposal of a new nomogram for predicting upstaging in contemporary D’Amico low-risk prostate cancer patients

Springer Science and Business Media LLC - Tập 35 - Trang 189-197 - 2016
Sami-Ramzi Leyh-Bannurah1,2, Paolo Dell’Oglio1,3, Zhe Tian1,4, Jonas Schiffmann1,5, Shahrokh F. Shariat6, Nazareno Suardi3, Montorsi Francesco3, Briganti Alberto3, Hans Heinzer2, Hartwig Huland2, Markus Graefen2, Lars Budäus2, Pierre I. Karakiewicz1
1Cancer Prognostics and Health Outcomes Unit, University of Montreal Health Center, Montreal, Canada
2Martini-Clinic, Prostate Cancer Center Hamburg-Eppendorf, Hamburg, Germany
3Department of Urology and Division of Experimental Oncology, URI, Urological Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy
4Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada
5Department of Urology, Academic Hospital Braunschweig, Brunswick, Germany
6Department of Urology, Medical University of Vienna, Vienna, Austria

Tóm tắt

Unfavorable prostate cancer (PCa) disease at final pathology affects at least 10 % of D’Amico low-risk patients. Thus, conservative therapies including active surveillance may be wrongfully applied. The purposes were to assess the rate of upstaging in a contemporary cohort of D’Amico low-risk PCa patients and to develop and externally validate a nomogram as upstaging prediction tool in two European cohorts. Analyses were restricted to 2007 patients who harbored low-risk PCa at ≥10-cores initial biopsy according to D’Amico classification (PSA <10.0 ng/ml, Gleason score <7 and clinical stage ≤T2a). Patients underwent radical prostatectomy at a high-volume center in Hamburg, Germany, from 2010 to 2015. The Hamburg cohort was randomly divided into development (n = 1338) and validation cohorts (n = 669). The development cohort was used to devise a nomogram predicting upstaging, defined as presence of ≥pT3 and/or lymph node invasion. The nomogram was externally validated in two European validation cohorts (Hamburg, n = 669; Milan, n = 465). Upstaging was observed in 187/1338 (14.0 %) of low-risk patients. In multivariable models, four of ten tested variables achieved independent predictor status: age (OR 1.07, 95 % CI 1.04–1.09), PSA (OR 1.21, 95 % CI 1.12–1.31), prostate volume (OR 0.97, 95 % CI 0.96–0.98) and percentage of positive cores (OR 1.02, 95 % CI 1.01–1.03). In external validation, the nomogram demonstrated 70.8 % (Hamburg) and 70.0 % (Milan) accuracy, respectively, with excellent concordance between predicted and observed values. Our proposed nomogram is capable to accurately identify D’Amico low-risk patients at risk of upstaging, utilizing four routinely available clinical variables, age, PSA, prostate volume and percentage of positive biopsy cores. Unfavorable prostate cancer disease at final pathology affects at least 10 % of D’Amico low-risk patients. Thus, we developed and externally validated a new nomogram based on contemporary low-risk prostate cancer patients to accurately identify D’Amico low-risk patients at risk of upstaging. It utilizes four routine variables, age, PSA, prostate volume and percentage of positive biopsy cores.

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