Abstract 1432P
Background
The efficacy and safety of laparoscopic distal D2 radical gastrectomy for the treatment of locally advanced gastric cancer patients (LAGC) who have received neoadjuvant chemotherapy (NAC) is a topic of ongoing debate. The objective of this study was to ascertain the safety of laparoscopic distal D2 radical gastrectomy in treating gastric cancer patients after NAC with locally advanced disease (cT3-4a, N-/+, M0).
Methods
This prospective, multicenter, single-arm clinical trial (ClinicalTrials.gov Identifiers: NCT03468712) was conducted at 14 hospital centers in China. Adults aged 18-75 years with histologically confirmed LAGC (cT3-4a, N-/+, M0) were enrolled in the study. Participants received 3 cycles of administration of intravenous oxaliplatin (130 mg/m2 on day 1 of each cycle) plus oral capecitabine (1000 mg/m2 twice daily on days 1 to 14 of each cycle) prior to undergoing laparoscopic distal gastrectomy. The primary endpoint was the postoperative overall morbidity rate. Secondary endpoints included postoperative mortality rate, surgery-related complication, R0 resection rate, completion rate of laparoscopic surgery, response of neoadjuvant chemotherapy, adverse event rate of neoadjuvant chemotherapy.
Results
A total of 153 patients were included in the final analysis. The study reported a postoperative overall morbidity rate of 20.9% (95%CI: 15.2%-28.0%), with postoperative mortality rate of 0%. Lung infections are the most common complication (9.2%). The surgery-related complication rate was 4.6% (95%CI: 2.2%-9.2%). Ten patients exhibited elevated levels of body fluid amylase without presenting any clinical symptoms or undergoing clinical intervention. The R0 resection rate occurred 100%. The completion rate of laparoscopic surgery was 98.7% (95%CI: 95.4%-99.6%). 9.2% patients achieved pathological complete response following NAC. The overall incidence of adverse effects after NAC was 20.3% (95%CI: 14.7%-27.3%).
Conclusions
The laparoscopic distal D2 radical gastrectomy demonstrated a favorable safety profile in the treatment of gastric cancer patients with advanced disease (cT3-4a, N-/+, M0) following neoadjuvant chemotherapy.
Clinical trial identification
NCT03468712.
Editorial acknowledgement
Legal entity responsible for the study
K. Yang and Jianku Hu.
Funding
1. 3. 5 project for disciplines of excellence, West China Hospital, Sichuan University (No. ZYJC21006).
Disclosure
The author has declared no conflicts of interest.
Resources from the same session
1154P - Prospective multinational evaluation of alkylating-induced hypermutation in neuroendocrine neoplasms (NEN): Clinical and molecular profiles associated with response to immune checkpoint inhibitors (CPI)
Presenter: Elena Trevisani
Session: Poster session 17
1156P - The efficacy of lower doses of everolimus in patients with advanced neuroendocrine tumors
Presenter: Rachel Riechelmann
Session: Poster session 17
1157P - Retreatment with peptide receptor radionuclide therapy (PRRT) in patients (p) with neuroendocrine tumors (NET): Spanish clinical experience from SEPTRALU national registry
Presenter: Jorge Hernando Cubero
Session: Poster session 17
1158P - A novel nomogram for predicting overall survival of small intestinal neuroendocrine tumors treated with PRRT
Presenter: Dimitrios Papantoniou
Session: Poster session 17
1159P - Molecular characterization of extra-pulmonary mixed adeno-neuroendocrine carcinomas: The NIRVANA substudy
Presenter: Francesca Spada
Session: Poster session 17
1160P - An Italian multicenter phase II trial of metronomic temozolomide in unfit patients with advanced neuroendocrine neoplasms: Interim analysis of the MeTe study
Presenter: Francesca Spada
Session: Poster session 17
1161P - Progression-free survival ratio and the implications for treatment sequencing in neuroendocrine neoplasms
Presenter: Philipp Melhorn
Session: Poster session 17
1162P - Transcriptomic analysis of gastroenteropancreatic neuroendocrine tumours with carcinoid syndrome
Presenter: Javier Pozas Perez
Session: Poster session 17
1163P - Prognostic value of systemic inflammatory index (SII) in neuroendocrine tumors (NETs) treated with peptide receptor radionuclide therapy (PRRT)
Presenter: Eduardo Terán Brage
Session: Poster session 17