Asia-Pacific journal of clinical oncology
October 18, 2026 · via Europe PMC
Minimum 7-Year Follow-Up of a Prospective Phase II Trial of Preoperative S-1 Plus Oxaliplatin Chemotherapy for Clinical Stage III Gastric Cancer.
Konishi S, Manaka D, Yoshida Y, +6 more, Fujii S.
AI summary — for doctors, generated from the abstract only
Two cycles of preoperative SOX before laparoscopic D2 gastrectomy for stage III gastric cancer showed good compliance and 5-year OS of 61.8% at 7+ years follow-up.
What was studied
Long-term follow-up of a single-arm phase II trial of 34 patients with clinical stage III gastric cancer given two cycles of preoperative S-1 plus oxaliplatin, then laparoscopic D2 gastrectomy and adjuvant therapy.
Key findings
- Preoperative SOX completion was 100%, with clinical and pathological response rates of 73.5% and 58.8% and R0 resection in 97.1%
- Adjuvant therapy was completed in 61.8%
- Five-year OS was 61.8% and RFS 58.8%, with ypN status and neutrophil-to-lymphocyte ratio exploratory prognostic factors
Clinical relevance
Supports perioperative-style chemotherapy with SOX as feasible and effective in locally advanced gastric cancer.
Who should care
Limitations
Small single-arm trial without a comparator, and prognostic associations were exploratory.
Preoperative SOX is a reasonable option to discuss in multidisciplinary review, but randomized evidence is needed.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
Aim
We report long-term outcomes from a prospective Phase II trial of two cycles of preoperative S-1 plus oxaliplatin (SOX) chemotherapy in patients with clinical Stage III gastric cancer (GC), with at least 7 years of follow-up for all surviving patients.
Methods
Patients received two cycles of preoperative SOX followed by laparoscopic D2 gastrectomy and postoperative adjuvant therapy. Overall survival (OS), relapse-free survival (RFS), treatment compliance, and clinically documented late adverse events were evaluated. Associations between clinicopathological factors and survival were explored using Kaplan-Meier analysis and the log-rank test.
Results
Thirty-four patients were analyzed. Preoperative SOX completion was 100%, with clinical and pathological response rates of 73.5% and 58.8%, respectively. R0 resection was achieved in 97.1%, and adjuvant therapy was initiated in 94.1% and completed in 61.8%. At analysis, 18 patients had died and 16 remained alive; all survivors had at least 7 years of follow-up and none were lost to follow-up. Five-year OS and RFS were 61.8% and 58.8%, respectively. In exploratory analyses, ypN0-1 status and a preoperative neutrophil-to-lymphocyte ratio <Â 4.3 were associated with better OS and RFS. No severe treatment-related late adverse events were documented during routine follow-up, although late toxicities were not systematically assessed.
Conclusion
Two-cycle preoperative SOX was highly feasible, with high treatment compliance and favorable long-term outcomes in this prospective single-arm cohort. Associations of ypN status and preoperative neutrophil-to-lymphocyte ratio with long-term outcomes were exploratory and require validation in larger comparative studies.
Trial registration
UMIN000036139.
DOI
10.1111/ajco.70214
PMID
42894432
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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