MedPath

Bicistronic CD19/CD22 CAR T-Cell Therapy Shows Durable Responses in Pediatric B-ALL

7 months ago3 min read

Key Insights

  • Bicistronic CD19/CD22-directed CAR T-cell therapy (B019) demonstrates safety and high remission rates in children with relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL).

  • The 1-year event-free survival (EFS) rate was 75.5%, and the 1-year overall survival (OS) rate was 93.5% among patients treated with the therapy.

  • Patients undergoing bridging bone marrow transplant after CAR T-cell expansion showed improved 1-year EFS rates compared to those without transplant (89.7% vs 76.8%).

Treatment with bicistronic CD19/CD22-directed CAR T-cell therapy (B019) has shown promising results in children with relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL), according to data from a phase 2 trial presented at the 2024 ASH Annual Meeting. The therapy demonstrated a high remission rate and durable responses, offering a potential new treatment option for this challenging patient population.

Efficacy and Survival Rates

The study, which included 343 pediatric patients, reported a 1-year event-free survival (EFS) rate of 75.5% and a 1-year overall survival (OS) rate of 93.5%. Notably, patients who underwent bridging bone marrow transplant following CAR T-cell expansion had improved 1-year EFS rates (89.7%) compared to those who did not (76.8%). However, the 1-year OS rates were similar between the two groups (95.8% vs 95.2%).
Hua Zhang, MD, PhD, vice president and chief scientific officer at SPH Biotherapeutics (HK), Limited, noted that "After CAR T-cell therapy, we have found that the 1-year EFS [rate] is higher [with] CAR T-cell treatment plus bone marrow transplant than CAR T-cell treatment alone, [although the] 1-year OS [rates were] very similar between these 2 [populations]."

Cytokine Release Syndrome (CRS)

While most patients experienced cytokine release syndrome (CRS), the severity of CRS was correlated with EFS outcomes. Patients with lower-grade CRS (grade 1/2) had a 1-year EFS rate of 80.9%, while those with higher-grade CRS (grade 3/4) had a 1-year EFS rate of 69.9% (P = .0191). Zhang also noted that the severity of CRS was highly correlated with disease burden and CAR T-cell viability, but not with the study dose range of infused cells.

Trial Design and Patient Characteristics

The phase 2 trial enrolled patients aged 0 to 18 years with relapsed/refractory B-ALL. Following enrollment, patients underwent debulking and lymphodepletion before receiving the CAR T-cell infusion at a dose of 1 x 106/kg to 10 x 106/kg. The study included patients with isolated extramedullary disease (n = 51) and those with refractory/isolated/combined hematologic relapse (n = 292).

Complete Remission Rates

Complete remissions (CRs) were achieved across all patients in the isolated extramedullary relapse cohort. In the refractory/isolated/combined hematologic relapse cohort, all but one patient with isolated bone marrow relapse achieved a CR; this patient died prior to evaluation.

Future Directions

Based on these promising results, a phase 1 study of the bicistronic CD19/CD22 CAR T-cell therapy is currently underway. Investigators plan to enroll 12 to 18 patients to further evaluate the safety and efficacy of this novel treatment approach.
Subscribe Icon

Stay Updated with Our Daily Newsletter

Get the latest pharmaceutical insights, research highlights, and industry updates delivered to your inbox every day.

Clinical Trials

Related research and studies

Related News

Sources

© Copyright 2025. All Rights Reserved by MedPath