ArticleESMO gastrointestinal oncology2026
Zolbetuximab plus pembrolizumab and chemotherapy in CLDN18.2-positive, HER2-negative, PD-L1-positive gastric or gastroesophageal junction adenocarcinoma: randomized, double-blind, phase III LUCERNA trial.
Article in ESMO gastrointestinal oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Late-phase strategies to overcome limitations of PD-1/PD-L1 therapy: a clinical development trajectory through 2030.Frontiers in oncology · 2026Review
- A changing landscape in gastric cancer.CA: a cancer journal for cliniciansArticle
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
There remains an unmet need for additional treatment options for patients with human epidermal growth factor receptor 2 (HER2)-negative, locally advanced (LA) unresectable, or metastatic gastric or gastroesophageal junction (mG/GEJ) adenocarcinoma whose tumors are claudin 18 isoform 2 (CLDN18.2)-positive and programmed death-ligand 1 (PD-L1)-positive. The phase 2 ILUSTRO trial previously demonstrated promising clinical activity with the combination of zolbetuximab plus chemotherapy and checkpoint inhibitor therapy in patients with HER2-negative, LA unresectable, or mG/GEJ adenocarcinoma whose tumors were CLDN18.2-positive, warranting further exploration. In LUCERNA, a multicenter, double-blind, phase III trial, patients with HER2-negative, LA unresectable, or mG/GEJ adenocarcinoma whose tumors are CLDN18.2-positive and PD-L1-positive will be randomly assigned 1:1 to either first-line zolbetuximab plus pembrolizumab and chemotherapy (a capecitabine and oxaliplatin regimen, CAPOX; or a modified folinic acid, fluorouracil, and oxaliplatin regimen, mFOLFOX6) or placebo plus pembrolizumab and chemotherapy. The primary endpoint is overall survival. Key secondary endpoints are progression-free survival and objective response rate. Additional secondary endpoints include duration of response and safety. The results of this trial have the potential to support a new standard-of-care option in this patient population.
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