CD7 CAR-T Therapy Induced Remission in R/R T-Cell Acute Lymphoblastic Leukemia/Lymphoma

While survival rates of pediatric patients with cancer are greatly improved, researchers and clinici
While survival rates of pediatric patients with cancer are greatly improved, researchers and clinici
Preliminary results of a clinical trial investigating the efficacy of CAR-T therapy in pediatric patients with CD7+ ALL/lymphoma were presented at ASCO 2022.

Autologous CD7 chimeric antigen receptor T-cell (CAR-T) therapy was safe and effective at inducing remission in pediatric patients with refractory or relapsed (R/R) T-cell acute lymphoblastic leukemia (T-ALL)/lymphoma, according to results of a study presented at the 2022 ASCO Annual Meeting.

R/R T-ALL/lymphoma is associated with poor prognosis. A previous study found that donor-derived CD7 CAR-T cell therapy induced remission in patients, but some patients developed graft-versus-host disease (GVHD).

In this analysis (ClinicalTrials.gov Identifier: NCT04840875), the safety and efficacy of CD7 CAR-T therapy was evaluated in 5 patients with R/R CD7+ T-ALL/lymphoma who had no leukemia cells in peripheral blood. The CD7 CAR-T therapy included an endoplasmic reticulum anchor domain fused to a CD7 binding domain to prevent CD7 expression was given in a 3+3 dose escalation process.

Patients were mean age 3.8 years (range, 1.9 to 13), 3 patients had marrow disease, 1 had central nervous system-3 status, and 1 had mediastinal mass and blasts in pleural fluid.

Three patients developed cytokine release syndrome at a median onset of 5 days (range, 1 to 9).

No GVHD, neurotoxicity, or infection events were observed. Grade 3/4 hematologic toxicity occurred in all patients, recovering to grade 2 by day 30.

At 1-month postinfusion, 4 of the 5 patients had achieved complete remission. One patient underwent stem cell transplantation at 2.9 months postinfusion and had a CD7+ relapse at 1.4 months posttransplantation.

At the last follow-up, all 5 patients had detectable CAR transgene. All 4 responders had a decrease in CD7+ normal T-cells and increased CD7-negative T-cells.

The major limitation of this study was its small sample size.

The study authors concluded that autologous CD7 CAR-T therapy was effective at inducing remission without signs of GHVD in patients with R/R T-ALL/LBL.

Reference

Zhao L, Pan J, Tang K, et al. Autologous CD7-targeted CAR T-cell therapy for refractory or relapsed T-cell acute lymphoblastic leukemia/lymphoma. J Clin Oncol. 2022;40(suppl 16; abstr 7035). doi:10.1200/JCO.2022.40.16_suppl.7035