Oncological outcomes of patients with incidental pathological T3a stage small renal cell carcinoma after partial

Chunwoo Lee1, Dalsan You2, Sangjun Yoo2

  • 1Department of Urology, Gyeongsang National University Changwon Hospital, Gyeongsang National University School of Medicine, Changwon, Korea.

Abstract

Insights

Partial nephrectomy for small renal cell carcinomas (RCCs) shows similar oncological outcomes for pathological T1a and T3a stages. Tumor size predicts recurrence-free survival, but pT stage does not significantly impact outcomes.

Area of Science:

  • Urology
  • Oncology
  • Nephrology

Background:

  • Small renal cell carcinomas (RCCs) are often treated with partial nephrectomy (PN).
  • Understanding oncological outcomes based on pathological T stage is crucial for treatment planning.
  • Incidental pathological T3a (pT3a) lesions in small RCCs require evaluation compared to pT1a lesions.

Purpose of the Study:

  • To compare oncological outcomes of patients with pathological T1a (pT1a) small renal cell carcinomas (RCCs) versus incidental pathological T3a (pT3a) RCCs treated with partial nephrectomy (PN).

Main Methods:

  • Retrospective evaluation of 1367 patients undergoing PN for small RCCs (≤4 cm) between 1997 and 2014.
  • Kaplan-Meier method used for recurrence-free, cancer-specific, and overall survival estimation.
  • Cox regression analysis applied to determine prognostic significance of variables.

Main Results:

  • Out of 1367 patients, 1324 (96.8%) had pT1a and 43 (3.2%) had pT3a lesions.
  • 5- and 10-year recurrence-free survival rates were comparable: 98.0% vs 94.4% (pT1a) and 95.2% vs 95.2% (pT3a).
  • Multivariate analysis indicated tumor size as a significant predictor for recurrence-free and cancer-specific survival, but pT stage (pT3a vs. pT1a) was not significant for RFS, CSS, or OS.

Conclusions:

  • Pathological T3a stage disease in small RCCs treated with PN demonstrates similar oncological outcomes to pT1a stage disease.
  • These findings suggest that pT stage may not be as critical as tumor size in predicting outcomes for small RCCs treated with PN.