4.6 Article

Prediction of the peritoneal recurrence via the macroscopic diagnosis of the serosal invasion in patients with gastric cancer: Supplementary analysis of JCOG0110

Journal

EJSO
Volume 48, Issue 8, Pages 1753-1759

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ejso.2022.01.015

Keywords

Peritoneal recurrence; Macroscopic diagnosis; Serosal invasion; Survival

Funding

  1. Health Sciences Research Grants for Medical Frontier Strategy Research
  2. Health and Labor Sciences Research Grant for Clinical Cancer Research [H19-Gan-016]
  3. National Cancer Center Research and Development Fund from the Ministry of Health, Labour, and Welfare, Japan [23-A-16, 23-A-19, 26-A-4, 29-A-3, 2020-J-3]
  4. [11S-3]
  5. [11S-4]
  6. [14S-3]
  7. [14S-4]
  8. [17S-3]
  9. [17S-5]
  10. [20S-3]
  11. [20S-5]

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This study investigated the predictability of peritoneal recurrence and survival based on macroscopically and pathologically diagnosed serosal invasion. The results showed that both macroscopic and pathologic diagnoses were independent predictors of peritoneal recurrence, overall survival, and relapse-free survival.
Background: Indications for adjuvant chemotherapy for advanced gastric cancer are determined based on the pathological diagnosis. However, macroscopic diagnoses have been reported as predictors of peritoneal recurrence and survival. This study investigated the predictability of peritoneal recurrence and survival based on macroscopically (sT) and pathologically (pT) diagnosed serosal invasion to identify more sensitive predictors of peritoneal recurrence. Methods: This study included 396 patients who underwent R0 resection without adjuvant chemotherapy with S-1 in the JCOG0110 study. Tumor depth limited to the subserosa (SS) was defined as serosal in-vasion negative (T-), while tumors with serosal invasion (SE, SI) were defined as serosal invasion positive (T+). The predictability of peritoneal recurrence based on sT and pT was evaluated using the Fine and Gray model. Cox regression analyses were performed for overall survival (OS) and relapse-free survival (RFS) with sT or pT as covariates. Findings: A total of 150 patients (37.9%) were sT+ and 82 (26.3%) were pT+. Sixty-two patients (15.7%) were sT+/pT+, 88 (22.2%) were sT+/pT-, 20 (5.1%) were sT-/pT+, and 226 (57.1%) were sT-/pT-. Both sT and pT were found to be independent predictors of peritoneal recurrence, OS, and RFS. The 5-year RFS rates of sT+/pT+, sT+/pT-, sT-/pT+, and sT-/pT-patients were 45.2%, 63.6%, 55.0%, and 81.8%, respectively.

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