Long-term safety and efficacy outcomes of valoctocogene roxaparvovec gene transfer up to 6years post-treatment.

Abstract

Valoctocogene roxaparvovec uses an adeno-associated virus serotype 5 (AAV5) vector to transfer a factor VIII (FVIII) coding sequence to individuals with severe haemophilia A, providing bleeding protection. To assess safety and efficacy of valoctocogene roxaparvovec 5-6years post-treatment. In a phase 1/2 trial, adult male participants with severe haemophilia A (FVIII ≤1IU/dL) without FVIII inhibitors or anti-AAV5 antibodies received valoctocogene roxaparvovec and were followed for 6 (6×1013 vg/kg; n=7) and 5 (4×1013 vg/kg; n=6) years. Safety, including investigation of potential associations between a malignancy and gene therapy, and efficacy are reported. No new treatment-related safety signals emerged. During year 6, a participant in the 6×1013 vg/kg cohort was diagnosed with grade 2 parotid gland acinar cell carcinoma; definitive treatment was uncomplicated parotidectomy with lymph node dissection. Target enrichment sequencing of tumour and adjacent healthy tissue revealed low vector integration (8.25×10-5 per diploid cell). Integrations were not elevated in tumour samples, no insertions appeared to drive tumorigenesis, and no clonal expansion of integration-containing cells occurred. During all follow-ups, >90% decreases from baseline in annualised treated bleeds and FVIII infusion rates were maintained. At the end of years 6 and 5, mean FVIII activity (chromogenic assay) was 9.8IU/dL (median, 5.6IU/dL) and 7.6IU/dL (median, 7.1IU/dL) for the 6×1013 and 4×1013 vg/kg cohorts, respectively, representing proportionally smaller year-over-year declines than earlier timepoints. Valoctocogene roxaparvovec safety and efficacy profiles remain largely unchanged; genomic investigations showed no association with a parotid tumour.