Partial nephrectomy (PN) versus ablative therapies (AT) for T1a clear cell renal cell carcinoma (ccRCC): Analysis of 2,161 patients.

C Chang Gon Kim (Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea) J Jongsoo Lee T Taejun Lee (Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea) J Ji Soo Park Y Young Seuk Choi (Severance Hospital, Yonsei University Health System, Soeul, South Korea) W Woong Kyu Han (Department of Urology, Yonsei University College of Medicine, Seoul, South Korea) W Won Sik Jang (Department of Urology, Yonsei University College of Medicine, Seoul, South Korea) H Hyunho Han (Department of Urology, Yonsei University College of Medicine, Seoul, South Korea) J Ji Eun Heo S Sang Joon Shin (Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea, Seoul, South Korea) S Seung-Hoon Beom S Sejung Park (Songdang Institute for Cancer Research, Yonsei University College of Medicine, Seoul, South Korea) W Woo Sun Kwon J Jiyeon Lee (School of Integrated Technology, College of Computing) W Won Sik Ham (Department of Urology and Urological Science Institute, Yonsei University College of Medicine, Seoul, South Korea) H Hyung Woo Kim S Sun Young Rha

Abstract

459 Background: PN is considered the standard treatment for T1a ccRCC, whereas AT have been increasingly utilized as minimally invasive alternatives, particularly in patients with high surgical risk or impaired kidney function. However, comparative data on oncologic and kidney outcomes between these two strategies are limited. Methods: This retrospective study included 2,161 patients with clinical T1a ccRCC who underwent either PN (N = 2,045) or AT (N = 116) between January 2006 and December 2024. Baseline characteristics, survival outcomes, and renal functional preservation were evaluated in both the overall cohort and the propensity score–matched cohort to adjust for confounders. Kidney outcome events were defined as declines of ≥30%, ≥40%, or ≥50% in estimated glomerular filtration rate (eGFR) from baseline, respectively. Results: Before matching, patients in the PN group were younger (mean age 55.1 vs. 63.9 years, P < 0.001) and had higher body mass index (BMI) (mean BMI 25.3 vs. 24.4 kg/m², P = 0.004), whereas the AT group had a lower baseline eGFR level (84.7 vs. 90.6 mL/min/1.73 m², P = 0.014) and were more likely to have underlying hypertension (57.8% vs. 42.0%, P < 0.001) and diabetes (33.6% vs. 24.2%, P = 0.022). During the median follow–up duration of 66.3 months (95% confidence interval [CI] 64.0–68.5), locoregional recurrence (hazard ratio [HR] and 95% CI: not estimable, P < 0.001), distant recurrence (HR: 0.189, 95% CI: 0.072–0.500, P < 0.001), death (HR: 0.141, 95% CI: 0.085–0.235, P < 0.001) and kidney function decline (≥30% [HR: 0.220, 95% CI: 0.111–0.433, P < 0.001], ≥40% [HR: 0.124, 95% CI: 0.058–0.264, P < 0.001], or ≥50% [HR: 0.141, 95% CI: 0.052–0.383, P < 0.001] decline in eGFR from baseline) were significantly superior in the PN group compared to AT group. The superior oncologic outcomes and kidney function preservation of PN were consistently observed in the propensity score–matched cohort (n = 605; 489 treated with PN and 116 with AT): locoregional recurrence (HR and 95% CI: not estimable, P < 0.001), distant recurrence (HR: 0.186, 95% CI: 0.059–0.584, P = 0.004), death (HR: 0.275, 95% CI: 0.162–0.468, P < 0.001), and kidney function decline (≥30% [HR: 0.383, 95% CI: 0.196–0.748, P = 0.005], ≥40% [HR: 0.230, 95% CI: 0.101–0.525, P < 0.001], or ≥50% [HR: 0.164, 95% CI: 0.049–0.548, P = 0.003]). Conclusions: PN demonstrated superior oncologic control and kidney function preservation compared with AT in patients with T1a ccRCC. These findings strongly support that PN should be prioritized as the curative treatment approach whenever clinically feasible.

Article Details

Volume / Issue Vol. 44, Issue 7_suppl
Published March 01, 2026
Pages 459-459
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (17)

C

Chang Gon Kim

Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea

J

Jongsoo Lee

T

Taejun Lee

Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea

J

Ji Soo Park

Y

Young Seuk Choi

Severance Hospital, Yonsei University Health System, Soeul, South Korea

W

Woong Kyu Han

Department of Urology, Yonsei University College of Medicine, Seoul, South Korea

W

Won Sik Jang

Department of Urology, Yonsei University College of Medicine, Seoul, South Korea

H

Hyunho Han

Department of Urology, Yonsei University College of Medicine, Seoul, South Korea

J

Ji Eun Heo

S

Sang Joon Shin

Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea, Seoul, South Korea

S

Seung-Hoon Beom

S

Sejung Park

Songdang Institute for Cancer Research, Yonsei University College of Medicine, Seoul, South Korea

W

Woo Sun Kwon

J

Jiyeon Lee

School of Integrated Technology, College of Computing

W

Won Sik Ham

Department of Urology and Urological Science Institute, Yonsei University College of Medicine, Seoul, South Korea

H

Hyung Woo Kim

S

Sun Young Rha