Combining Cell Transplants or Gene Therapy With Deep Brain Stimulation for Parkinson's Disease

被引:18
作者
Rowland, Nathan C. [1 ]
Starr, Philip A. [1 ,3 ]
Larson, Paul S. [1 ,3 ]
Ostrem, Jill L. [2 ,3 ]
Marks, William J., Jr. [2 ,3 ]
Lim, Daniel A. [1 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA USA
[2] Univ Calif San Francisco, Dept Neurol, San Francisco Vet Affairs Med Ctr, San Francisco, CA USA
[3] Univ Calif San Francisco, San Francisco Vet Affairs Med Ctr, Parkinsons Dis Res Educ & Clin Ctr, San Francisco, CA 94143 USA
关键词
Parkinson's disease; stem cell technology; gene therapy; clinical trial design; deep brain stimulation; RANDOMIZED CONTROLLED-TRIAL; DOUBLE-BLIND; OPEN-LABEL; SUBTHALAMIC NUCLEUS; MEDICAL THERAPY; AAV2-NEURTURIN; DELIVERY; MOTOR;
D O I
10.1002/mds.26083
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cell transplantation and gene therapy each show promise to enhance the treatment of Parkinson's disease (PD). However, because cell transplantation and gene therapy generally require direct delivery to the central nervous system, clinical trial design involves unique scientific, ethical, and financial concerns related to the invasive nature of the procedure. Typically, such biologics have been tested in PD patients who have not received any neurosurgical intervention. Here, we suggest that PD patients undergoing deep brain stimulation (DBS) device implantation are an ideal patient population for the clinical evaluation of cell transplantation and gene therapy. Randomizing subjects to an experimental group that receives the biologic concurrently with the DBS implantationor to a control group that receives the DBS treatment alonehas several compelling advantages. First, this study design enables the participation of patients likely to benefit from DBS, many of whom simultaneously meet the inclusion criteria of biologic studies. Second, the need for a sham neurosurgical procedure is eliminated, which may reduce ethical concerns, promote patient recruitment, and enhance the blinding of surgical trials. Third, testing the biologic by piggybacking onto an established, reimbursable procedure should reduce the cost of clinical trials, which may allow a greater number of biologics to reach this critical stage of research translation. Finally, this clinical trial design may lead to combinatorial treatment strategies that provide PD patients with more durable control over disabling motor symptoms. By combining neuromodulation with biologics, we may also reveal important treatment paradigms relevant to other diseases of the brain. (c) 2014 International Parkinson and Movement Disorder Society
引用
收藏
页码:190 / 195
页数:6
相关论文
共 34 条
[1]   Safety/feasibility of targeting the substantia nigra with AAV2-neurturin in Parkinson patients [J].
Bartus, Raymond T. ;
Baumann, Tiffany L. ;
Siffert, Joao ;
Herzog, Christopher D. ;
Alterman, Ron ;
Boulis, Nicholas ;
Turner, Dennis A. ;
Stacy, Mark ;
Lang, Anthony E. ;
Lozano, Andres M. ;
Olanow, C. Warren .
NEUROLOGY, 2013, 80 (18) :1698-1701
[2]  
Carmona-Torre F, 2013, NEW ENGL J MED, V368, P2037, DOI [10.1056/NEJMoa1205158, 10.1056/NEJMc1303485]
[3]   Ten-Year Outcome of Subthalamic Stimulation in Parkinson Disease [J].
Castrioto, Anna ;
Lozano, Andres M. ;
Poon, Yu-Yan ;
Lang, Anthony E. ;
Fallis, Melanie ;
Moro, Elena .
ARCHIVES OF NEUROLOGY, 2011, 68 (12) :1550-1556
[4]   Micro Lesion Effect of the Globus Pallidus Internus and Outcome with Deep Brain Stimulation in Patients with Parkinson Disease and Dystonia [J].
Cersosimo, Maria G. ;
Raina, Gabriela B. ;
Benarroch, Eduardo E. ;
Piedimonte, Fabian ;
Gonzalez Aleman, Gabriela ;
Micheli, Federico E. .
MOVEMENT DISORDERS, 2009, 24 (10) :1488-1493
[5]   Safety and tolerability of putaminal AADC gene therapy for Parkinson disease [J].
Christine, C. W. ;
Starr, P. A. ;
Larson, P. S. ;
Eberling, J. L. ;
Jagust, W. J. ;
Hawkins, R. A. ;
VanBrocklin, H. F. ;
Wright, J. F. ;
Bankiewicz, K. S. ;
Aminoff, M. J. .
NEUROLOGY, 2009, 73 (20) :1662-1669
[6]   Parkinson's Disease: Gene Therapies [J].
Coune, Philippe G. ;
Schneider, Bernard L. ;
Aebischer, Patrick .
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE, 2012, 2 (04)
[7]   A randomized trial of deep-brain stimulation for Parkinson's disease [J].
Deuschl, Guenther ;
Schade-Brittinger, Carmen ;
Krack, Paul ;
Volkmann, Jens ;
Schaefer, Helmut ;
Boetzel, Kai ;
Daniels, Christine ;
Deutschlaender, Angela ;
Dillmann, Ulrich ;
Eisner, Wilhelm ;
Gruber, Doreen ;
Hamel, Wolfgang ;
Herzog, Jan ;
Hilker, Ruediger ;
Klebe, Stephan ;
Kloss, Manja ;
Koy, Jan ;
Krause, Martin ;
Kupsch, Andreas ;
Lorenz, Delia ;
Lorenzl, Stefan ;
Mehdorn, H. Maximilian ;
Moringlane, Jean Richard ;
Oertel, Wolfgang ;
Pinsker, Marcus O. ;
Reichmann, Heinz ;
Reuss, Alexander ;
Schneider, Gerd-Helge ;
Schnitzler, Alfons ;
Steude, Ulrich ;
Sturm, Volker ;
Timmermann, Lars ;
Tronnier, Volker ;
Trottenberg, Thomas ;
Wojtecki, Lars ;
Wolf, Elisabeth ;
Poewe, Werner ;
Voges, Juergen .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (09) :896-908
[8]   The placebo treatments in neurosciences - New insights from clinical and neuroimaging studies [J].
Diederich, Nico J. ;
Goetz, Christopher G. .
NEUROLOGY, 2008, 71 (09) :677-684
[9]   Motor and cognitive outcome in patients with Parkinson's disease 8 years after subthalamic implants [J].
Fasano, Alfonso ;
Romito, Luigi M. ;
Daniele, Antonio ;
Piano, Carla ;
Zinno, Massimiliano ;
Bentivoglio, Anna Rita ;
Albanese, Alberto .
BRAIN, 2010, 133 :2664-2676
[10]   Transplantation of embryonic dopamine neurons for severe Parkinson's disease. [J].
Freed, CR ;
Greene, PE ;
Breeze, RE ;
Tsai, WY ;
DuMouchel, W ;
Kao, R ;
Dillon, S ;
Winfield, H ;
Culver, S ;
Trojanowski, JQ ;
Eidelberg, D ;
Fahn, S .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (10) :710-719