International validation of a preoperative nomogram for prostate cancer recurrence after radical prostatectomy

被引:161
作者
Graefen, M
Karakiewicz, PI
Cagiannos, I
Quinn, DI
Henshall, SM
Grygiel, JJ
Sutherland, RL
Stricker, PD
Klein, E
Kupelian, P
Skinner, DG
Lieskovsky, G
Bochner, B
Huland, H
Hammerer, PG
Haese, A
Erbersdobler, A
Eastham, JA
de Kernion, J
Cangiano, T
Schröder, FH
Wildhagen, MF
van der Kwast, TH
Scardino, PT
Kattan, MW
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Urol, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Biostat, New York, NY 10021 USA
[3] Garvan Inst Med Res, Sydney, NSW, Australia
[4] St Vincents Hosp, Sydney, NSW 2010, Australia
[5] Cleveland Clin, Cleveland, OH 44106 USA
[6] Univ So Calif, Los Angeles, CA USA
[7] Univ Calif Los Angeles, Los Angeles, CA USA
[8] Univ Hosp, Hamburg, Germany
[9] Louisiana State Univ, Hlth Sci Ctr, Shreveport, LA 71105 USA
[10] Erasmus Univ, Dept Urol, NL-3000 DR Rotterdam, Netherlands
[11] Acad Hosp, Rotterdam, Netherlands
关键词
D O I
10.1200/JCO.2002.12.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We evaluated the predictive accuracy of a recently published preoperative nomogram for prostate cancer that predicts 5-year freedom from recurrence. We applied this nomogram to patients from seven different institutions spanning three continents. Methods: Clinical data of 6,754 patients were supplied for validation, and 6,232 complete records were used. Nomogram-predicted probabilities of 60-month freedom from recurrence were compared with actual follow-up in two ways. First, areas under the receiver operating characteristic curves (AUCs) were determined for the entire data set according to several variables, including the institution where treatment was delivered. Second, nomogram classification-based risk quadrants were compared with actual Kaplan-Meier plots. Results: The AUC for all institutions combined was 0.75, with individual institution AUCs ranging from 0.67 to 0.83. Nomogram predictions for each risk quadrant were similar to actual freedom from recurrence rates: predicted probabilities of 87% (low-risk group), 64% (intermediate-low-risk group), 39% (intermediate-high-risk group), and 14% (high-risk group) corresponded to actual rates of 86%, 64%, 42%, and 17%, respectively. The use of neoadjuvant therapy, variation in the prostate-specific antigen recurrence definitions between institutions, and minor differences in the way the Gleason grade was reported did not substantially affect the predictive accuracy of the nomogram. Conclusion: The nomogram is accurate when applied at international treatment institutions with similar patient selection and management strategies. Despite the potential for heterogeneity in patient selection and management, most predictions demonstrated high concordance with actual observations. Our results demonstrate that accurate predictions may be expected across different patient populations. (C) 2002 by American Society of Clinical Oncology.
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页码:3206 / 3212
页数:7
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