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January 14, 2026Journal of Clinical Oncology0 citations

Neoadjuvant, adjuvant and perioperative systemic therapies in gastric and gastroesophageal junction adenocarcinoma: A network meta-analysis of randomized controlled trials.

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RNRafael Lara NohmiIMIsadora MamedeTATurkan Aliyeva

Key Points

  • This research aims to compare the efficacy of various systemic therapies for resectable gastric adenocarcinoma.
  • Conducted a network meta-analysis of randomized controlled trials published until August 2025.
  • Included interventions like neoadjuvant, adjuvant, and perioperative chemotherapy combined with immune checkpoint inhibitors or antiangiogenic agents.
  • Extracted hazard ratios for event-free survival and overall survival from included trials.
  • In event-free survival, perioperative triplet chemotherapy plus immune checkpoint inhibitors demonstrated improved efficacy over certain regimens.
  • For overall survival, the same perioperative regimen showed significant improvement compared to adjuvant triplet chemotherapy and neoadjuvant triplet chemotherapy.
  • Perioperative triplet chemotherapy plus immune checkpoint inhibitors achieved the highest ranking for both event-free and overall survival.

Abstract

390 Background: Surgery alone often provides suboptimal outcomes for patients with locally advanced (LA) gastric and gastroesophageal junction (G/GEJ) adenocarcinoma, and additional perioperative therapy is required to improve survival outcomes. Recent evidence favors systemic treatment with perioperative chemotherapy (CT) over neoadjuvant chemoradiotherapy. Given the range of systemic therapies in this setting, we conducted a network meta-analysis (NMA) to compare their efficacy in resectable LA G/GEJ adenocarcinoma. Methods: A systematic review identified randomized controlled trials published up to August 20th, 2025, that enrolled patients with resectable G/GEJ adenocarcinoma. Eligible interventions included surgery combined with adjuvant, neoadjuvant, or perioperative CT ± immune checkpoint inhibitors (ICIs) or antiangiogenic agents. Trials evaluating radiotherapy were excluded. Hazard ratios (HR) for event-free survival (EFS) and overall survival (OS) were extracted or reconstructed. A Bayesian NMA with random-effects models (200,000 iterations, 20,000 burn-ins, 4 chains) was performed. HRs with 95% credible intervals (CrIs) were generated. Treatment rankings were assessed using the surface under the cumulative ranking curve (SUCRA). Results: A total of 50 trials (57 reports, 17,841 patients) were included. The most frequent comparators were surgery alone and adjuvant doublet CT. Data from 35 trials (15,328 patients) contributed to EFS analyses (16 regimens). Perioperative triplet CT + ICI showed a trend toward improved efficacy compared with perioperative triplet CT alone (HR 0.71; 95% CrI 0.50–1.00) and was superior to adjuvant triplet CT (HR 0.50; 95% CrI 0.30–0.79), but not to perioperative doublet CT + ICI (HR 0.76; 95% CrI 0.42–1.30). In ranking analyses for EFS, perioperative triplet CT + ICI had the highest SUCRA (0.94), followed by neoadjuvant triplet CT + adjuvant monotherapy CT (0.87) and perioperative doublet CT + ICI (0.76). For OS, 48 trials (16,601 patients) were analyzed (16 regimens). Perioperative triplet CT + ICI improved OS versus adjuvant triplet CT (HR 0.58; 95% CrI 0.35–0.94) and neoadjuvant triplet CT (HR 0.45; 95% CrI 0.23–0.88), but not versus perioperative triplet CT (HR 0.78; 95% CrI 0.53–1.14) or perioperative doublet CT + ICI (HR 0.82; 95% CrI 0.44–1.49). In ranking analyses for OS, perioperative triplet CT + ICI achieved the highest SUCRA (0.94), followed by perioperative doublet CT + ICI (0.81) and perioperative triplet CT (0.78). Conclusions: Perioperative triplet CT + ICI achieved the most favorable SUCRA for EFS and OS, supporting this therapy as a potentially preferred systemic strategy for LA G/GEJ adenocarcinoma. However, overlapping CrIs of this regimen with perioperative triplet and perioperative doublet CT + ICI highlight residual uncertainty.

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Cite This Study

Nohmi et al. (2026) studied this question.

synapsesocial.com/papers/6966f33213bf7a6f02c00fdfhttps://doi.org/10.1200/jco.2026.44.2_suppl.390
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Efficacy and Safety of Systemic Regimens for Resectable Gastric and Gastroesophageal Junction Adenocarcinoma: A Network Meta-analysis of Randomized Controlled Trials2026
  2. 2Comparative efficacy and safety of neoadjuvant and perioperative systemic therapies for resectable locally advanced gastric and gastroesophageal junction adenocarcinoma: a network meta analysis of randomized controlled trials2026
  3. 3Comparative effectiveness of perioperative strategies for resectable gastric and gastroesophageal junction cancer: a Bayesian network meta-analysis2025
  4. 4Neoadjuvant immunotherapy for locally advanced resectable gastric and gastroesophageal junction adenocarcinoma: a systematic review and meta-analysis2026
  5. 5The Landmark Series: Neoadjuvant Therapy for Patients with Resectable Gastroesophageal Junction Adenocarcinomas2026