Frontiers in Surgery (Sep 2022)

Accuracy of preoperative clinical staging for locally advanced gastric cancer in KLASS-02 randomized clinical trial

  • Dong Jin Kim,
  • Woo Jin Hyung,
  • Young-Kyu Park,
  • Hyuk-Joon Lee,
  • Ji Yeong An,
  • Hyoung-Il Kim,
  • Hyung-Ho Kim,
  • Seung Wan Ryu,
  • Hoon Hur,
  • Min-Chan Kim,
  • Seong-Ho Kong,
  • Jin-Jo Kim,
  • Do Joong Park,
  • Do Joong Park,
  • Keun Won Ryu,
  • Young Woo Kim,
  • Jong Won Kim,
  • Joo-Ho Lee,
  • Han-Kwang Yang,
  • Sang-Uk Han,
  • Wook Kim,
  • on behalf of the Korean Laparoendoscopic Gastrointestinal Surgery Study (KLASS) Group

DOI
https://doi.org/10.3389/fsurg.2022.1001245
Journal volume & issue
Vol. 9

Abstract

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PurposeThe discrepancy between preoperative and final pathological staging has been a long-standing challenge for the application of clinical trials or appropriate treatment options. This study aimed to demonstrate the accuracy of preoperative staging of locally advanced gastric cancer using data from a large-scale randomized clinical trial.Materials and methodsOf the 1050 patients enrolled in the clinical trial, 26 were excluded due to withdrawal of consent (n = 20) or non-surgery (n = 6). The clinical and pathological staging was compared. Risk factor analysis for underestimation was performed using univariate and multivariate analyses.ResultsRegarding T staging by computed tomography, accuracy rates were 74.48, 61.62, 58.56, and 85.16% for T1, T2, T3 and T4a, respectively. Multivariate analysis for underestimation of T staging revealed that younger age, ulcerative gross type, circular location, larger tumor size, and undifferentiated histology were independent risk factors. Regarding nodal status estimation, 54.9% of patients with clinical N0 disease were pathologic N0, and 36.4% of patients were revealed to have pathologic N0 among clinical node-positive patients. The percentage of metastasis involvement at the D1, D1+, and D2 lymph node stations significantly increased with the advanced clinical N stage. Among all patients, 29 (2.8%), including 26 with peritoneal seeding, exhibited distant metastases.ConclusionsEstimating the exact pathologic staging remains challenging. A thorough evaluation is mandatory before treatment selection or trial enrollment. Moreover, we need to set a sufficient case number when we design the clinical trial considering the stage migration.

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