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Predicting Disease Recurrence, Early Progression, and Overall Survival Following Surgical Resection for High-risk Localized and Locally Advanced Renal Cell Carcinoma

  • Andres F. Correa
  • , Opeyemi A. Jegede
  • , Naomi Haas
  • , Keith T. Flaherty
  • , Michael Pins
  • , Adebowale Adeniran
  • , Edward M. Messing
  • , Judith Manola
  • , Christopher G. Wood
  • , Christopher J. Kane
  • , Michael A.S. Jewett
  • , Janice P. Dutcher
  • , Robert S. DiPaola
  • , Michael A. Carducci
  • , Robert G. Uzzo
  • Dana-Farber Cancer Institute
  • Abramson Cancer Center of the University of Pennsylvania
  • University of Pennsylvania
  • Massachusetts General Hospital Cancer Center
  • Massachusetts General Hospital
  • Harvard University
  • Advocate Health Care
  • University of Illinois at Chicago
  • Yale University
  • University of Rochester
  • Brigham and Women's Hospital
  • University of Texas MD Anderson Cancer Center
  • University of Texas Health Science Center at Houston
  • University of California at San Diego
  • University of Toronto
  • Princess Margaret Cancer Centre
  • University Health Network
  • Cancer Research Foundation
  • New York Medical College
  • Our Lady of Mercy Medical Center
  • Montefiore Health System
  • Rutgers - The State University of New Jersey, New Brunswick
  • University of Kentucky
  • Johns Hopkins University

Research output: Contribution to journal › Article › peer-review

63 Scopus citations

Abstract

Background: Risk stratification for localized renal cell carcinoma (RCC) relies heavily on retrospective models, limiting their generalizability to contemporary cohorts. Objective: To introduce a contemporary RCC prognostic model, developed using prospective, highly annotated data from a phase III adjuvant trial. Design, setting, and participants: The model utilizes outcome data from the ECOG-ACRIN 2805 (ASSURE) RCC trial. Outcome measurements and statistical analysis: The primary outcome for the model is disease-free survival (DFS), with overall survival (OS) and early disease progression (EDP) as secondary outcomes. Model performance was assessed using discrimination and calibration tests. Results and limitations: A total of 1735 patients were included in the analysis, with 887 DFS events occurring over a median follow-up of 9.6 yr. Five common tumor variables (histology, size, grade, tumor necrosis, and nodal involvement) were included in each model. Tumor histology was the single most powerful predictor for each model outcome. The C-statistics at 1 yr were 78.4% and 81.9% for DFS and OS, respectively. Degradation of the DFS, DFS validation set, and OS model's discriminatory ability was seen over time, with a global c-index of 68.0% (95% confidence interval or CI [65.5, 70.4]), 68.6% [65.1%, 72.2%], and 69.4% (95% CI [66.9%, 71.9%], respectively. The EDP model had a c-index of 75.1% (95% CI [71.3, 79.0]). Conclusions: We introduce a contemporary RCC recurrence model built and internally validated using prospective and highly annotated data from a clinical trial. Performance characteristics of the current model exceed available prognostic models with the added benefit of being histology inclusive and TNM agnostic. Patient summary: Important decisions, including treatment protocols, clinical trial eligibility, and life planning, rest on our ability to predict cancer outcomes accurately. Here, we introduce a contemporary renal cell carcinoma prognostic model leveraging high-quality data from a clinical trial. The current model predicts three outcome measures commonly utilized in clinical practice and exceeds the predictive ability of available prognostic models.

Original languageEnglish
Pages (from-to)20-31
Number of pages12
JournalEuropean Urology
Volume80
Issue number1
DOIs
StatePublished - Jul 2021

Keywords

  • Carcinoma, Renal Cell/surgery
  • Disease-Free Survival
  • Humans
  • Kidney Neoplasms/surgery
  • Neoplasm Recurrence, Local
  • Prognosis
  • Prospective Studies
  • Retrospective Studies

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