A Novel T-Stage Classification System for Adrenocortical Carcinoma: Proposal from the US Adrenocortical Carcinoma Study Group

  • Caroline E. Poorman
  • , Cecilia G. Ethun
  • , Lauren M. Postlewait
  • , Thuy B. Tran
  • , Jason D. Prescott
  • , Timothy M. Pawlik
  • , Tracy S. Wang
  • , Jason Glenn
  • , Ioannis Hatzaras
  • , Rivfka Shenoy
  • , John E. Phay
  • , Kara Keplinger
  • , Ryan C. Fields
  • , Linda X. Jin
  • , Sharon M. Weber
  • , Ahmed Salem
  • , Jason K. Sicklick
  • , Shady Gad
  • , Adam C. Yopp
  • , John C. Mansour
  • Quan Yang Duh, Natalie Seiser, Carmen C. Solórzano, Colleen M. Kiernan, Konstantinos I. Votanopoulos, Edward A. Levine, Charles A. Staley, George A. Poultsides, Shishir K. Maithel

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Background: The 7th AJCC T-stage system for adrenocortical carcinoma (ACC), based on size and extra-adrenal invasion, does not adequately stratify patients by survival. Lymphovascular invasion (LVI) is a known poor prognostic factor. We propose a novel T-stage system that incorporates LVI to better risk-stratify patients undergoing resection for ACC. Method: Patients undergoing curative-intent resections for ACC from 1993 to 2014 at 13 institutions comprising the US ACC Group were included. Primary outcome was disease-specific survival (DSS). Results: Of the 265 patients with ACC, 149 were included for analysis. The current T-stage system failed to differentiate patients with T2 versus T3 disease (p = 0.10). Presence of LVI was associated with worse DSS versus no LVI (36 mo vs. 168 mo; p = 0.001). After accounting for the individual components of the current T-stage system (size, extra-adrenal invasion), LVI remained a poor prognostic factor on multivariable analysis (hazard ratio 2.14, 95% confidence interval 1.05–4.38, p = 0.04). LVI positivity further stratified patients with T2 and T3 disease (T2: 37 mo vs. median not reached; T3: 36 mo vs. 96 mo; p = 0.03) but did not influence survival in patients with T1 or T4 disease. By incorporating LVI, a new T-stage classification system was created: [T1: ≤ 5 cm, (−)local invasion, (+/−)LVI; T2: > 5 cm, (−)local invasion, (−)LVI OR any size, (+)local invasion, (−)LVI; T3: > 5 cm, (−)local invasion, (+)LVI OR any size, (+)local invasion, (+)LVI; T4: any size, (+)adjacent organ invasion, (+/−)LVI]. Each progressive new T-stage group was associated with worse median DSS (T1: 167 mo; T2: 96 mo; T3: 37 mo; T4: 15 mo; p < 0.001). Conclusions: Compared with the current T-stage system, the proposed T-stage system, which incorporates LVI, better differentiates T2 and T3 disease and accurately stratifies patients by disease-specific survival. If externally validated, this T-stage classification should be considered for future AJCC staging systems.

Original languageEnglish
Pages (from-to)520-527
Number of pages8
JournalAnnals of Surgical Oncology
Volume25
Issue number2
DOIs
StatePublished - Feb 1 2018

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