TY - JOUR
T1 - Hospital variation in the treatment of cT1a renal cancer
AU - for the Santeon RCC Working Group
AU - Bresser, Cato Caroline
AU - van der Nat, Paul Bastiaan
AU - Yildirim, Hilin
AU - Kersten, Bart Jean Pieter
AU - Leenarts, Hein Johannes Josephus
AU - Aben, Katja Karen Helmi
AU - Zondervan, Patricia Jeannelle
AU - Dijksman, Lea Magdalena
AU - Polm, Pepijn Dione
AU - Garvelink, Mirjam Marjolein
AU - van Melick, Harm Hubertus Edmundus
AU - Scheepens, Wouterus Antonius
AU - Dijkstra, Sybren
AU - Yska, Marit Josephine
AU - Luijendijk, Daphne
AU - Asselman, Marino
AU - Ruiter, Annebeth Evelien Cathelijn
N1 - Publisher Copyright:
© 2026 The Author(s). BJUI Compass published by John Wiley & Sons Ltd on behalf of BJU International Company.
PY - 2026/4
Y1 - 2026/4
N2 - Objectives: To evaluate treatment patterns and inter-hospital variation of cT1a renal cell carcinoma (RCC) in seven Dutch teaching hospitals. Patients and methods: In this historical multicenter cohort study, adults diagnosed with cT1a renal cancer (2019–2022) were identified through the Netherlands Cancer Registry. Clinical data were extracted from electronic records. Primary outcome was initial treatment. Descriptive statistics and subgroup analyses assessed variation. Logistic regression analyses identified factors associated with active treatment. Results: We included 501 patients with 544 cT1a renal cancer tumours. Mean age was 66 years, 40% were overweight (BMI 25–29.9), and 40% had severe comorbidity (CCI ≥ 5). Active treatment was initiated for 65% of tumours, ranging from 44% to 85% between hospitals (p < 0.001). The types of treatment modalities used differed significantly between hospitals. This variation persisted after stratifying for comorbidity and tumour complexity. Independent factors associated with active treatment were Charlson comorbidity index (CCI) (OR = 0.77 95%CI [0.72–0.83], p < 0.001) RENAL Nephrometry score (OR = 1.16 95%CI [1.04–1.28], p = 0.006), and hospital of diagnosis (p < 0.001). After adjustment for case mix, hospital of diagnosis remained a significant predictive factor (p < 0.001). Study limitations include potential selection bias and limited generalizability. Conclusions: Substantial inter-hospital variation exists in cT1a RCC management, which is not fully explained by patient- or tumour characteristics. To reduce unwarranted variation and improve care, transparent care pathways, routine outcome measurement, shared decision-making and inter-hospital benchmarking are needed.
AB - Objectives: To evaluate treatment patterns and inter-hospital variation of cT1a renal cell carcinoma (RCC) in seven Dutch teaching hospitals. Patients and methods: In this historical multicenter cohort study, adults diagnosed with cT1a renal cancer (2019–2022) were identified through the Netherlands Cancer Registry. Clinical data were extracted from electronic records. Primary outcome was initial treatment. Descriptive statistics and subgroup analyses assessed variation. Logistic regression analyses identified factors associated with active treatment. Results: We included 501 patients with 544 cT1a renal cancer tumours. Mean age was 66 years, 40% were overweight (BMI 25–29.9), and 40% had severe comorbidity (CCI ≥ 5). Active treatment was initiated for 65% of tumours, ranging from 44% to 85% between hospitals (p < 0.001). The types of treatment modalities used differed significantly between hospitals. This variation persisted after stratifying for comorbidity and tumour complexity. Independent factors associated with active treatment were Charlson comorbidity index (CCI) (OR = 0.77 95%CI [0.72–0.83], p < 0.001) RENAL Nephrometry score (OR = 1.16 95%CI [1.04–1.28], p = 0.006), and hospital of diagnosis (p < 0.001). After adjustment for case mix, hospital of diagnosis remained a significant predictive factor (p < 0.001). Study limitations include potential selection bias and limited generalizability. Conclusions: Substantial inter-hospital variation exists in cT1a RCC management, which is not fully explained by patient- or tumour characteristics. To reduce unwarranted variation and improve care, transparent care pathways, routine outcome measurement, shared decision-making and inter-hospital benchmarking are needed.
KW - cT1a renal cancer
KW - hospital variation
KW - Netherlands Cancer Registry
KW - practice variation
KW - renal cell carcinoma
UR - https://www.scopus.com/pages/publications/105035674383
U2 - 10.1002/bco2.70130
DO - 10.1002/bco2.70130
M3 - Article
C2 - 41971150
AN - SCOPUS:105035674383
SN - 2688-4526
VL - 7
JO - BJUI compass
JF - BJUI compass
IS - 4
M1 - e70130
ER -