A double‐blind controlled trial of bilateral fetal nigral transplantation in Parkinson's disease

CW Olanow, CG Goetz, JH Kordower… - Annals of …, 2003 - Wiley Online Library
Annals of neurology, 2003Wiley Online Library
Thirty‐four patients with advanced Parkinson's disease participated in a prospective 24‐
month double‐blind, placebo‐controlled trial of fetal nigral transplantation. Patients were
randomized to receive bilateral transplantation with one or four donors per side or a placebo
procedure. The primary end point was change between baseline and final visits in motor
component of the Unified Parkinson's Disease Rating Scale in the practically defined off
state. There was no significant overall treatment effect (p= 0.244). Patients in the placebo …
Abstract
Thirty‐four patients with advanced Parkinson's disease participated in a prospective 24‐month double‐blind, placebo‐controlled trial of fetal nigral transplantation. Patients were randomized to receive bilateral transplantation with one or four donors per side or a placebo procedure. The primary end point was change between baseline and final visits in motor component of the Unified Parkinson's Disease Rating Scale in the practically defined off state. There was no significant overall treatment effect (p = 0.244). Patients in the placebo and one‐donor groups deteriorated by 9.4 ± 4.25 and 3.5 ± 4.23 points, respectively, whereas those in the four‐donor group improved by 0.72 ± 4.05 points. Pairwise comparisons were not significant, although the four‐donor versus placebo groups yielded a p value of 0.096. Stratification based on disease severity showed a treatment effect in milder patients (p = 0.006). Striatal fluorodopa uptake was significantly increased after transplantation in both groups and robust survival of dopamine neurons was observed at postmortem examination. Fifty‐six percent of transplanted patients developed dyskinesia that persisted after overnight withdrawal of dopaminergic medication (“off”‐medication dyskinesia). Fetal nigral transplantation currently cannot be recommended as a therapy for PD based on these results.Ann Neurol 2003;54:403–414
Wiley Online Library