Departments of1Neurological Surgery.
2The Miami Project to Cure Paralysis; and.
Neurosurg Focus. 2019 Mar 1;46(3):E8. doi: 10.3171/2018.12.FOCUS18593.
OBJECTIVEIn cell transplantation trials for spinal cord injury (SCI), quantifiable imaging criteria that serve as inclusion criteria are important in trial design. The authors' institutional experience has demonstrated an overall high rate of screen failures. The authors examined the causes for trial exclusion in a phase I, open-lab clinical trial examining the role of autologous Schwann cell intramedullary transplantation. Specifically, they reviewed the imaging characteristics in people with chronic SCI that excluded applicants from the trial, as this was a common cause of screening failures in their study.METHODSThe authors reviewed MRI records from 152 people with chronic (> 1 year) SCI who volunteered for intralesional Schwann cell transplantation but were deemed ineligible by prospectively defined criteria. Rostral-caudal injury lesion length was measured along the long axis of the spinal cord in the sagittal plane on T2-weighted MRI. Other lesion characteristics, specifically those pertaining to lesion cavity structure resulting in trial exclusion, were recorded.RESULTSImaging records from 152 potential participants with chronic SCI were reviewed, 42 with thoracic-level SCI and 110 with cervical-level SCI. Twenty-three individuals (55%) with thoracic SCI and 70 (64%) with cervical SCI were not enrolled in the trial based on imaging characteristics. For potential participants with thoracic injuries who did not meet the screening criteria for enrollment, the average rostral-caudal sagittal lesion length was 50 mm (SD 41 mm). In applicants with cervical injuries who did not meet the screening criteria for enrollment, the average sagittal lesion length was 34 mm (SD 21 mm).CONCLUSIONSWhile screening people with SCI for participation in a cell transplantation clinical trial, lesion length or volume can exclude potential subjects who appear appropriate candidates based on neurological eligibility criteria. In planning future cell-based therapy trials, the limitations incurred by lesion size should be considered early due to the screening burden and impact on candidate selection.
在脊髓损伤(SCI)的细胞移植试验中,作为纳入标准的可量化成像标准在试验设计中非常重要。作者所在机构的经验表明,筛选失败率总体较高。作者研究了一期、开放实验室临床试验中排除自体雪旺细胞髓内移植试验参与者的原因,该试验旨在研究雪旺细胞移植的作用。具体来说,他们回顾了慢性 SCI 患者的影像学特征,这些特征使他们不符合试验条件,这是他们研究中筛选失败的常见原因。
作者回顾了 152 名慢性(> 1 年)SCI 患者的 MRI 记录,这些患者自愿接受腔内雪旺细胞移植,但根据前瞻性定义的标准被认为不符合条件。在矢状面 T2 加权 MRI 上沿脊髓长轴测量损伤病变的头尾长度。记录其他病变特征,特别是与导致试验排除的病变腔结构有关的特征。
对 152 名有慢性 SCI 潜在参与者的影像学记录进行了回顾,其中 42 名胸段 SCI,110 名颈段 SCI。根据影像学特征,23 名(55%)胸段 SCI 患者和 70 名(64%)颈段 SCI 患者未被纳入试验。对于不符合纳入筛选标准的胸段损伤潜在参与者,平均矢状位病变长度为 50mm(SD 41mm)。对于不符合纳入筛选标准的颈段损伤潜在参与者,平均矢状位病变长度为 34mm(SD 21mm)。
在筛选有 SCI 的人参与细胞移植临床试验时,病变长度或体积可能会排除那些根据神经学资格标准看起来是合适候选者的人。在计划未来基于细胞的治疗试验时,由于筛选负担和对候选者选择的影响,应尽早考虑病变大小带来的限制。