Eighteen-year survival after GD2-directed Chimeric Antigen Receptor-Modified Immune Effector Cell Treatment for Neuroblastoma.
Helen E HeslopChe-Hsing LiSandhya SharmaAndras A HeczeyDavid SteffinChrystal LouisBambi GrilleySachin ThakkarMeng-Fen WuNicholas WangCliona RooneyMalcolm BrennerPublished in: Research square (2024)
We report long-term outcomes up to 18 years of a clinical trial treating children with neuroblastoma with EBV-specific T lymphocytes and CD3-activated T cells - each expressing a first-generation chimeric antigen receptor targeting GD2 with barcoded transgenes to allow tracking of each population. Of 11 patients with active disease at infusion, three patients achieved a complete response that was sustained in 2, one for 8 years until lost to follow up and one for 18+ years. Of eight patients with a history of relapse or at high risk of recurrence, five are disease-free at their last follow-up between 10-14 years post-infusion. Intermittent low levels of transgene were detected during the follow up period with significantly greater persistence in those who were long-term survivors. In conclusion, patients with relapsed/refractory neuroblastoma achieved long-term disease control after receiving GD2 CAR-T cell therapy including one patient now in remission of relapsed disease for >18 years.
Keyphrases
- cell therapy
- clinical trial
- acute myeloid leukemia
- acute lymphoblastic leukemia
- end stage renal disease
- stem cells
- young adults
- multiple myeloma
- low dose
- chronic kidney disease
- mesenchymal stem cells
- newly diagnosed
- prognostic factors
- epstein barr virus
- peritoneal dialysis
- case report
- randomized controlled trial
- dendritic cells
- drug delivery
- bone marrow
- immune response
- replacement therapy