Predicting 15-year prostate cancer specific mortality after radical prostatectomy.
Predicting 15-year prostate cancer specific mortality after radical prostatectomy.
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DOI:
10.1016/j.juro.2010.10.057
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发表时间:
2011-03
期刊:
影响因子:
--
通讯作者:
Stephenson AJ
中科院分区:
文献类型:
--
作者:
Eggener SE;Scardino PT;Walsh PC;Han M;Partin AW;Trock BJ;Feng Z;Wood DP;Eastham JA;Yossepowitch O;Rabah DM;Kattan MW;Yu C;Klein EA;Stephenson AJ
Long-term prostate cancer-specific mortality (PCSM) after radical prostatectomy is poorly defined in the era of widespread screening. An understanding of the treated natural history of screen-detected cancers and the pathological risk factors for PCSM are needed for treatment decision-making. Using Fine and Gray competing risk regression analysis, the clinical and pathological data and follow-up information of 11,521 patients treated by radical prostatectomy at four academic centers from 1987 to 2005 were modeled to predict PCSM. The model was validated on 12,389 patients treated at a separate institution during the same period. The overall 15-year PCSM was 7%. Primary and secondary pathological Gleason grade 4–5 (P < 0.001 for both), seminal vesicle invasion (P < 0.001), and year of surgery (P = 0.002) were significant predictors of PCSM. A nomogram predicting 15-year PCSM based on standard pathological parameters was accurate and discriminating with an externally-validated concordance index of 0.92. Stratified by patient age, 15-year PCSM for Gleason score ≤ 6, 3+4, 4+3, and 8–10 ranged from 0.2–1.2%, 4.2–6.5%, 6.6–11%, and 26–37%, respectively. The 15-year PCSM risks ranged from 0.8–1.5%, 2.9–10%, 15–27%, and 22–30% for organ-confined cancer, extraprostatic extension, seminal vesicle invasion, and lymph node metastasis, respectively. Only 3 of 9557 patients with organ-confined, Gleason score ≤ 6 cancers have died from prostate cancer. The presence of poorly differentiated cancer and seminal vesicle invasion are the prime determinants of PCSM after radical prostatectomy. The risk of PCSM can be predicted with unprecedented accuracy once the pathological features of prostate cancer are known.
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影响因子:
6.6
作者:
Porter, Christopher R.;Kodama, Koichi;Karakiewicz, Pierre I.
通讯作者:
Karakiewicz, Pierre I.
影响因子:
8.8
作者:
Cuzick, J.;Fisher, G.;Kattan, M. W.;Berney, D.;Oliver, T.;Foster, C. S.;Moller, H.;Reuter, V.;Fearn, P.;Eastham, J.;Scardino, P.
通讯作者:
Scardino, P.
DOI:
10.1093/jnci/djg043
发表时间:
2003-09-17
期刊:
JOURNAL OF THE NATIONAL CANCER INSTITUTE
影响因子:
--
作者:
D'Amico, AV;Moul, JW;Chen, MH
通讯作者:
Chen, MH
影响因子:
120.7
作者:
Albertsen, PC;Hanley, JA;Fine, J
通讯作者:
Fine, J
影响因子:
2.1
作者:
Dong, Fel;Reuther, Alwyn M.;Klein, Eric A.
通讯作者:
Klein, Eric A.