This pilot clinical study aims to evaluate the effectiveness of Chimeric Antigen Receptor (CAR) T-cell therapy in treating severe, refractory systemic lupus erythematosus (SLE), an autoimmune disease driven by autoreactive B-cells. Current treatments for severe SLE, including glucocorticoids, cytotoxic, and immunosuppressive drugs, have significant limitations. These treatments do not adequately control the underlying autoimmune process and require long-term use, leading to chronic side effects and often failing to prevent permanent organ damage. Given the high prevalence and mortality rates associated with SLE in regions like Asia and Malaysia, there is a pressing need for more effective therapies.
This study seeks to investigate CAR-T cell therapy's potential for treating severe treatment-refractory systemic lupus erythematosus (SLE) in Malaysian patients. STUDY OBJECTIVES General Objective: To evaluate the safety and efficacy of autologous CD19 CAR T-cell infusion in patients with severe refractory SLE. Specific Objectives: To evaluate the safety and tolerability of treatment. To evaluate efficacy as measured by response rates and survival. To evaluate the quality of life based on the use of validated health questionnaire tools. Hypothesis: Intravenous autologous CD19 CAR T-cell therapy is safe, and efficacious in patients with severe refractory SLE. EXPECTED OUTCOME OF THE STUDY: CD19 CAR T-cell therapy is expected to result in: Clinical remission as assessed by DORIS remission) with a good safety profile Serologic remission (defined as negative anti-dsDNA and normal complement C3 and C4 levels) at 3 months Sustained DORIS remission for at least 12 months Improvement in organ function Prolongation of duration of drug-free remission Improvement in quality of life Manageable adverse effects STUDY POPULATION This pilot study will be conducted between 2025 and 2028 involving 5 patients diagnosed with severe, treatment-refractory SLE. Eligibility criteria were based on previously published studies and international guidelines for CAR treatment for patients with autoimmune disease (Boulougoura et al., 2023).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
Study participant will be given single infusion of autologous CD19 CAR-T cells following lymphodepletion chemotherapy
University Kebangsaan Malaysia Medical Center
Bandar Tun Razak, Kuala Lumpur, Malaysia
RECRUITINGRate of Adverse events
Incidence of adverse event (AE), classified according to CTCAE version 5.0, and evaluation and classification of Cytokine Release Syndrome (CRS) and Immune Effector cell-associated Neurotoxicity Syndrome (ICANS)
Time frame: Starting form day 0 up to 24 months after CAR-T cells infusion
SLEDAI Remission Rate
Remission is evaluated by fulfilment of SLEDAI remission criteria
Time frame: Weeks 4, 8, 12, 16, 20, 24,28 after CAR-T cells infusion
Clinical Response Rate
Measured by BILAG, PGA, SLICC/ACR
Time frame: Weeks 4, 8, 12, 16, 20, 24,28 after CAR-T cells infusion
Rate of B cell aplasia
Numbers of B cells in peripheral blood measured by flow cytometry
Time frame: Months 1, 3, 6, 9, 12, 15, 18, 21, 24 after CAR-T cells infusion
Rate of Immunological response
Changes in the levels of SLE-associated serum autoantibodies
Time frame: Months 1, 3, 6, 9, 12, 15, 18, 21, 24 after CAR-T cells infusion
Mean of Quality of life score
Quality of life Assessed by FACIT-F
Time frame: Weeks 4, 8, 12, 16, 20, 24,28 after CAR-T cells infusion
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