TPS462 Background: GC/GEJC is the fifth most commonly diagnosed cancer and the fourth leading cause of cancer-related death worldwide (Sung H, et al. CA Cancer J Clin 2021). Prognosis is poor in GC GEJC; median overall survival (OS) is less than 10 months in the 2L setting and less than 6 months in the 3L+ setting (Wilke H, et al. Lancet Oncol 2014; Shitara K, et al. Lancet Oncol 2018). New treatment options are needed. CLDN18.2 has emerged as a new therapeutic target in GC/GEJC. Sone ve, a potential first-in-class CLDN18.2-targeted antibody conjugated to monomethyl auristatin E via a protease cleavable linker, has demonstrated clinical activity in a Phase 1 study in advanced GC/GEJC (Xu R-H, et al. J Clin Oncol 2023). CLARITY-Gastric 01 (NCT06346392) is a randomized, open-label, sponsor-blinded, global Phase 3 study that will assess the efficacy and safety of sone ve versus investigator’s (INV) choice of therapy after ≥1 prior therapy for advanced GC / GEJC expressing CLDN18.2. Methods: Participants (pts) will be randomized 1:1:1 to sone ve dose level 1 intravenous (IV) every three weeks (Q3W; Arm 1), sone ve dose level 2 IV Q3W (Arm 2), or INV choice of therapy (2L: ramucirumab ram + paclitaxel PTX, PTX, or docetaxel for pts with contraindication to ram only; 3L+: irinotecan, TAS-102 excluding China, or apatinib China only; Arm 3). As of January 2025, the sone ve monotherapy dose was determined to be 2.2 mg/kg (Arm 2). Arm 1 was closed for enrollment. Randomization will continue in a 1:1 ratio to Arm 2 and Arm 3. Eligible pts must have histologically confirmed, unresectable, locally advanced or metastatic GC/GEJC (non-HER2+, CLDN18.2 expression ≥25% tumor cells with membranous staining at any intensity for CLDN18.2). Pts must have disease progression on / after ≥1 prior regimen (including platinum-fluoropyrimidine) and have an ECOG performance status of 0 or 1. Pts previously treated with CLDN18.2-targeting therapy (other than naked monoclonal antibody) are excluded. Recruitment has begun and pts are planned to be enrolled across 16 countries in Asia, Europe, and North America. Dual primary endpoints are progression-free survival (PFS; intent-to-treat ITT pts) and OS (3L+ pts). The secondary endpoints include OS (ITT pts), PFS (3L+ pts), objective response rate and duration of response (ITT and 3L+ pts), and safety / tolerability. Efficacy data will be summarized and analyzed in the ITT population. All efficacy endpoints will assess the selected sone ve dose arm versus Arm 3. Safety and tolerability will be assessed in all pts who receive ≥1 dose of study treatment. Previously presented at European Society for Medical Oncology Gastrointestinal Cancers Congress 2024, Final Publication Number: 495TiP, Kohei Shitara, et al. - Reused with permission. Clinical trial information: NCT06346392 .
Shitara et al. (Sat,) studied this question.