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Updated: Aug 22, 2025
![Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F62334.jpg&w=3840&q=50)
Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
[Tisagenlecleucel for relapsed/refractory diffuse large B-cell lymphoma: real-world data from single institute
Yu Yagi1, Yusuke Kanemasa1, Yuki Sasaki1
1Department of Medical Oncology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
Chimeric antigen receptor (CAR) T-cell therapy with tisagenlecleucel demonstrates high efficacy and a manageable safety profile in patients with relapsed or refractory diffuse large B-cell lymphoma (r/r DLBCL). Real-world data show comparable outcomes to clinical trials, even in patients with comorbidities.
Area of Science:
- Hematology
- Oncology
- Immunotherapy
Context:
- Chimeric antigen receptor (CAR) T-cell therapy represents a significant advancement in treating relapsed or refractory diffuse large B-cell lymphoma (r/r DLBCL).
- Real-world data are crucial for understanding the effectiveness and safety of CAR T-cell therapies in diverse patient populations beyond clinical trial criteria.
Purpose:
- This study retrospectively evaluated the safety and effectiveness of commercially available tisagenlecleucel in patients with r/r DLBCL treated at a single institution.
- The analysis aimed to assess response rates, survival outcomes, and adverse events, including cytokine release syndrome (CRS) and cytopenias, in a real-world setting.
Summary:
- Twenty-one patients with r/r DLBCL received tisagenlecleucel. High rates of any-grade (85.7%) and severe (9.5%) cytokine release syndrome (CRS) were observed, managed with tocilizumab and/or glucocorticoids.
- The 3-month complete response (CR) rate was 61.9%. At 6 months, progression-free survival (PFS) was 53.1% and overall survival (OS) was 69.2%.
- Severe cytopenias and hypogammaglobulinemia were frequent. Importantly, comorbidities did not significantly impact CR, PFS, or adverse event rates, suggesting tisagenlecleucel's efficacy and safety are maintained in a broader patient group.
Impact:
- Tisagenlecleucel demonstrated high efficacy and a manageable safety profile in the real-world treatment of r/r DLBCL, consistent with pivotal trial findings.
- The study highlights the therapy's effectiveness even in patients with comorbidities, potentially expanding treatment eligibility.
- These findings support the use of tisagenlecleucel as a valuable therapeutic option for r/r DLBCL in routine clinical practice.
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