TY - JOUR
T1 - Classification tree for the prediction of malignant disease and the prediction of non-diagnostic biopsies in patients with small renal masses
AU - Organ, Michael
AU - MacDonald, Landan P.
AU - Jewett, Michael A.S.
AU - Ajzenberg, Henry
AU - Almatar, Ashraf
AU - Abdolell, Mohamed
AU - Acker, Matthew R.
AU - Rendon, Ricardo
N1 - Publisher Copyright:
© 2019 Canadian Urological Association.
PY - 2019/4
Y1 - 2019/4
N2 - Introduction: Preoperative prediction of benign vs. malignant small renal masses (SRMs) remains a challenge. This study: 1) validates our previously published classification tree (CT) with an external cohort; 2) creates a new CT with the combined cohort; and 3) evaluates the RENAL and PADUA scoring systems for prediction of malignancy. Methods: This study includes a total of 818 patients with renal masses; 395 underwent surgical resection and 423 underwent biopsy. A CT to predict benign disease was developed using patient and tumour characteristics from the 709 eligible participants. Our CT is based on four parameters: tumour volume, symptoms, gender, and symptomatology. CART modelling was also used to determine if RENAL and PADUA scoring could predict malignancy. Results: When externally validated with the surgical cohort, the predictive accuracy of the old CT dropped. However, by combining the cohorts and creating a new CT, the predictive accuracy increased from 74% to 87% (95% confidence interval 0.84–0.89). RENAL and PADUA score alone were not predictive of malignancy. One limitation was the lack of available histological data from the biopsy series. Conclusions: The validated old CT and new combined-cohort CT have a predictive value greater than currently published nomograms and single-biopsy cohorts. Overall, RENAL and PADUA scores were not able to predict malignancy.
AB - Introduction: Preoperative prediction of benign vs. malignant small renal masses (SRMs) remains a challenge. This study: 1) validates our previously published classification tree (CT) with an external cohort; 2) creates a new CT with the combined cohort; and 3) evaluates the RENAL and PADUA scoring systems for prediction of malignancy. Methods: This study includes a total of 818 patients with renal masses; 395 underwent surgical resection and 423 underwent biopsy. A CT to predict benign disease was developed using patient and tumour characteristics from the 709 eligible participants. Our CT is based on four parameters: tumour volume, symptoms, gender, and symptomatology. CART modelling was also used to determine if RENAL and PADUA scoring could predict malignancy. Results: When externally validated with the surgical cohort, the predictive accuracy of the old CT dropped. However, by combining the cohorts and creating a new CT, the predictive accuracy increased from 74% to 87% (95% confidence interval 0.84–0.89). RENAL and PADUA score alone were not predictive of malignancy. One limitation was the lack of available histological data from the biopsy series. Conclusions: The validated old CT and new combined-cohort CT have a predictive value greater than currently published nomograms and single-biopsy cohorts. Overall, RENAL and PADUA scores were not able to predict malignancy.
UR - http://www.scopus.com/inward/record.url?scp=85066234632&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85066234632&partnerID=8YFLogxK
U2 - 10.5489/cuaj.5196
DO - 10.5489/cuaj.5196
M3 - Article
AN - SCOPUS:85066234632
SN - 1911-6470
VL - 13
SP - 115
EP - 119
JO - Journal of the Canadian Urological Association
JF - Journal of the Canadian Urological Association
IS - 4
ER -