BMC Cancer · 2024 · 23 citations · 24 references
MedicineOncologyPharmacologyChemotherapyGastrointestinal OncologyPrecision OncologyCancer ImmunotherapyEsophageal CancerGastrointestinal Cancer PharmacotherapyMetastatic Disease ManagementMetastatic Disease TreatmentSystemic Therapy For Gastrointestinal CancersEpidermal Growth Factor Receptor InhibitionEpidermal Growth Factor Receptor SignalingEsophageal Cancer PharmacotherapyGastric Cancer PharmacotherapyMetastatic Gastric CancerRandomized Clinical TrialsSystematic Literature ReviewTargeted Therapy-related Gastrointestinal Toxicity
BACKGROUND: The benefit of adding Zolbetuximab to the treatment in patients with Claudin-18 isoform 2 (CLDN18.2)-positive, human epidermal growth factor receptor 2-negative, locally advanced unresectable or metastatic gastric or gastro-oesophageal junction adenocarcinoma (GC/GEJ) is not yet fully elucidated. METHODS: We searched PubMed, Embase and Cochrane databases for randomized controlled trials (RCTs) that investigated Zolbetuximab plus chemotherapy versus chemotherapy alone for GC or GEJ adenocarcinoma. We computed hazard-ratios (HRs) or odds-ratios (ORs) for binary endpoints, with 95% confidence intervals (CIs). RESULTS: Three studies and 1,233 patients were included. Comparing with Zolbetuximab plus chemotherapy versus chemotherapy alone, progression-free survival (PFS) rate (HR 0.64; 95% CI 0.49-0.84; p < 0.01) and overall survival (OS) rate (HR 0.72; 95% CI 0.62-0.83; p < 0.01) were significant in favor of the Zolbetuximab group. Regarding effectiveness, the Objective Response Rate (ORR) was (OR 1.15; 95% CI 0.87-1.53; p = 0.34). CONCLUSIONS: In this comprehensive systematic review and meta-analysis of RCTs, the incorporation of Zolbetuximab alongside chemotherapy offers a promising prospect for reshaping the established treatment paradigms for patients diagnosed with advanced CLDN18.2-positive GC/GEJ cancer.
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Medicine, Oncology, Pharmacotherapy +17