ENT Institute and Otorhinolaryngology Department of Eye & ENT Hospital, Fudan University, Shanghai, China.
NHC Key Laboratory of Hearing Medicine, Fudan University, Shanghai, China.
Nat Med. 2024 Jul;30(7):1898-1904. doi: 10.1038/s41591-024-03023-5. Epub 2024 Jun 5.
Gene therapy is a promising approach for hereditary deafness. We recently showed that unilateral AAV1-hOTOF gene therapy with dual adeno-associated virus (AAV) serotype 1 carrying human OTOF transgene is safe and associated with functional improvements in patients with autosomal recessive deafness 9 (DFNB9). The protocol was subsequently amended and approved to allow bilateral gene therapy administration. Here we report an interim analysis of the single-arm trial investigating the safety and efficacy of binaural therapy in five pediatric patients with DFNB9. The primary endpoint was dose-limiting toxicity at 6 weeks, and the secondary endpoint included safety (adverse events) and efficacy (auditory function and speech perception). No dose-limiting toxicity or serious adverse event occurred. A total of 36 adverse events occurred. The most common adverse events were increased lymphocyte counts (6 out of 36) and increased cholesterol levels (6 out of 36). All patients had bilateral hearing restoration. The average auditory brainstem response threshold in the right (left) ear was >95 dB (>95 dB) in all patients at baseline, and the average auditory brainstem response threshold in the right (left) ear was restored to 58 dB (58 dB) in patient 1, 75 dB (85 dB) in patient 2, 55 dB (50 dB) in patient 3 at 26 weeks, and 75 dB (78 dB) in patient 4 and 63 dB (63 dB) in patient 5 at 13 weeks. The speech perception and the capability of sound source localization were restored in all five patients. These results provide preliminary insights on the safety and efficacy of binaural AAV gene therapy for hereditary deafness. The trial is ongoing with longer follow-up to confirm the safety and efficacy findings. Chinese Clinical Trial Registry registration: ChiCTR2200063181 .
基因治疗是遗传性耳聋的一种有前途的方法。我们最近表明,携带人类 OTOF 转基因的单侧 AAV1-hOTOF 基因治疗与双重腺相关病毒(AAV)血清型 1 联合使用是安全的,并与常染色体隐性耳聋 9(DFNB9)患者的功能改善相关。随后修改并批准了该方案,以允许进行双侧基因治疗。在这里,我们报告了一项单臂试验的中期分析,该试验研究了双侧治疗在 5 名 DFNB9 儿科患者中的安全性和疗效。主要终点是 6 周时的剂量限制毒性,次要终点包括安全性(不良事件)和疗效(听觉功能和言语感知)。没有发生剂量限制毒性或严重不良事件。共发生 36 例不良事件。最常见的不良事件是淋巴细胞计数增加(36 例中有 6 例)和胆固醇水平升高(36 例中有 6 例)。所有患者均双侧听力恢复。所有患者在基线时右(左)耳平均听性脑干反应阈值均>95dB(>95dB),26 周时,1 例患者右(左)耳平均听性脑干反应阈值恢复至 58dB(58dB),2 例患者恢复至 75dB(85dB),3 例患者恢复至 55dB(50dB),4 例患者恢复至 75dB(78dB),5 例患者恢复至 63dB(63dB)。所有 5 名患者的言语感知和声源定位能力均得到恢复。这些结果提供了双侧 AAV 基因治疗遗传性耳聋安全性和疗效的初步见解。该试验正在进行中,随访时间更长,以确认安全性和疗效发现。中国临床试验注册中心注册号:ChiCTR2200063181 。