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CAR-T Therapy for Gastric Cancer

CAR-T Therapy for Gastric Cancer

CAR-T cell therapy is a cutting-edge personalized immunotherapy that is being actively applied to the treatment of gastric cancer. BIOOCUS has developed CAR-T products targeting gastric cancer-specific antigens such as Claudin18.2 and HER2, showing significant efficacy in patients who have failed multiple prior treatments—for example, CT041 achieved an ORR of 57.1%, DCR of 75%, and a 6-month overall survival rate of 81.2%. Leveraging an international GMP-grade platform, a multidisciplinary expert team, and extensive global clinical experience, BIOOCUS provides a safe, effective, and comprehensive CAR-T therapy solution for gastric cancer patients.

Advantages

  • Highly Specific Targeting: By directing CAR-T cells against CLDN18.2 or HER2, gastric cancer cells can be precisely identified and eliminated, minimizing off-tumor effects.

  • Overcoming Multiline Treatment Resistance: In CT041 trials, the gastric cancer cohort achieved an objective response rate (ORR) of 57.1%, disease control rate (DCR) of 75.0%, and a 6-month overall survival (OS) of 81.2% in patients who had failed multiple prior lines of therapy.

  • Durable Responses: CLDN18.2-CAR-T treatment yielded a 6-month duration of response rate of 44.8%, suggesting potential for long-term clinical benefit.

  • Personalized Therapy: Using the patient’s own T cells reduces the risk of rejection and enhances safety and efficacy.

Treatment Process

  • Peripheral Blood T-Cell Collection
    T cells are isolated from the patient’s peripheral blood via leukapheresis.

  • Genetic Engineering
    In a GMP-compliant laboratory, T cells are transduced to express a CAR targeting CLDN18.2 or HER2, then expanded ex vivo.

  • Lymphodepleting Conditioning
    A preparative regimen of cyclophosphamide and fludarabine is administered to deplete endogenous lymphocytes and create a favorable niche for CAR-T cell expansion.

  • CAR-T Cell Infusion
    The engineered CAR-T cells are infused back into the patient intravenously.

  • Monitoring and Management
    After infusion, patients are closely monitored for cytokine release syndrome (CRS) and neurotoxicity, with timely interventions as needed.

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