Efficacy and Safety of Sequential CD19 and CD22 CAR-T Therapy in Adult B-ALL
Author Information
Author(s): Tingting Yang, Yetian Dong, Mingming Zhang, Jingjing Feng, Shan Fu, Pingnan Xiao, Ruimin Hong, Huijun Xu, Jiazhen Cui, Simao Huang, Guoqing Wei, Delin Kong, Geng Jia, Alex H. Chang
Primary Institution: First Affiliated Hospital of Zhejiang University
Hypothesis
This study aimed to evaluate the efficacy and safety of sequential CD19 and CD22 CAR-T cell therapy in adult patients with relapsed/refractory B-cell acute lymphoblastic leukemia.
Conclusion
Sequential CAR-T cell therapy demonstrated durable efficacy and a manageable safety profile in relapsed/refractory B-ALL.
Supporting Evidence
- High-risk cytogenetic and genomic aberrations were identified in 43.5% of patients.
- The median overall survival was not reached with a median follow-up of 19.4 months.
- 91.3% of patients were alive at 1 year, and 58.6% at 2 years.
- Leukemia-free survival rates were 67.1% at 1 year and 47.0% at 2 years.
- Cytokine release syndrome occurred in 78.3% of patients after CD19 CAR-T therapy.
Takeaway
This study shows that using two types of CAR-T therapy can help adults with a tough type of leukemia feel better and live longer.
Methodology
The study evaluated the efficacy and safety of sequential CD19 and CD22 CAR-T cell therapy in adult patients with R/R B-ALL, focusing on adverse events, overall survival, and leukemia-free survival.
Potential Biases
The variability in prior treatments and the single-arm design may introduce biases.
Limitations
The study had a small sample size and was conducted at a single center, which may limit the generalizability of the findings.
Participant Demographics
The median age of participants was 58.1 years, with 52.2% male and 47.8% female.
Statistical Information
P-Value
0.021
Confidence Interval
95% CI [80.5–100%] at 1 year, 95% CI [38.7–88.8%] at 2 years
Statistical Significance
p<0.05
Digital Object Identifier (DOI)
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