TY - JOUR
T1 - Behavioural outcomes of subthalamic stimulation and medical therapy versus medical therapy alone for Parkinson's disease with early motor complications (EARLYSTIM trial)
T2 - secondary analysis of an open-label randomised trial
AU - Lhommée, Eugénie
AU - Wojtecki, Lars
AU - Czernecki, Virginie
AU - Witt, Karsten
AU - Maier, Franziska
AU - Tonder, Lisa
AU - Timmermann, Lars
AU - Hälbig, Thomas D.
AU - Pineau, Fanny
AU - Durif, Franck
AU - Witjas, Tatiana
AU - Pinsker, Marcus
AU - Mehdorn, Maximilian
AU - Sixel-Döring, Friederike
AU - Kupsch, Andreas
AU - Krüger, Rejko
AU - Elben, Saskia
AU - Chabardès, Stephan
AU - Thobois, Stéphane
AU - Brefel-Courbon, Christine
AU - Ory-Magne, Fabienne
AU - Regis, Jean Marie
AU - Maltête, David
AU - Sauvaget, Anne
AU - Rau, Jörn
AU - Schnitzler, Alfons
AU - Schüpbach, Michael
AU - Schade-Brittinger, Carmen
AU - Deuschl, Gunther
AU - Houeto, Jean Luc
AU - Krack, Paul
AU - Negovanska, Velina
AU - Welter, Marie Laure
AU - Corvol, Jean Christophe
AU - Agid, Yves
AU - Navarro, Soledad
AU - Meier, Niklaus
AU - Hartmann, Andreas
AU - Hesekamp, Helke
AU - Cornu, Philippe
AU - Möller, Bettina
AU - Nebel, Adelheid
AU - Raethjen, Jan
AU - Knudsen, Karina
AU - Volkmann, Jens
AU - Falk, Daniela
AU - Paschen, Steffen
AU - Meister, Ingo
AU - Kuhn, Jens
AU - Donner, Kerstin
AU - EARLYSTIM study group
N1 - Funding Information:
EL was reimbursed congress fees and travel expenses to participate in a scientific meeting from Medtronic during the study. FP received grants from Novartis. DM received consultancy fees from Novartis Pharma, UCB Pharma, and Medtronic France during the study. ST received grants from France Parkinson and Fondation pour la Recherche Médicale; grants and personal fees from Medtronic during the study; personal fees from Aguettant, Boston, and UCB; travel grants from Abbvie; and personal fees and non-financial support from TEVA. LW received speaker honoraria from Medtronic during the study. ASc received financial support from University of Kiel, during the study; has served as a consultant for Medtronic, Boston Scientific, St Jude Medical, and Grünenthal; and has received lecture fees from Abbvie, Boston Scientific, St Jude Medical, Medtronic, UCB, MEDA Pharma, Teva Pharma, and GlaxoSmithKline. FS-D has received honoraria for speaking engagements from Abbvie, Bayer, Boehringer Ingelheim, Desitin, GlaxoSmithKline, Licher MT, Medtronic, Novartis, UCB, and Zambon; was reimbursed congress fees by Licher MT, Abbvie, and Mundipharm; and has served on an advisory board for UCB. FO-M was reimbursed congress fees and travel expenses to participate in a scientific meeting by Medtronic during the study. CB-C has served on advisory boards of Aguettant, Orkyn, and Zambon; and has received contracts from Aguettant, Lundbeck, Teva, Medtronic, Zambon, and UCB. MP has received speaking fees from and had congress fees and travel expenses reimbursed by Medtronic during the study. KW reports reimbursement of congress fees from BIAL and Desitin; and grants from the Federal Ministry of Education and Research and the German Research Foundation. RK has received research grants from the German Research Council, the Michael J Fox Foundation, the Fritz Thyssen Foundation, the Federal Ministry for Education and Research, and the Fonds National de Recherche de Luxembourg; and has received speaker's honoraria and travel grants from Abbvie, B Braun, St Jude Medical, and Medtronic. J-LH received grants from Programme Hospitalier de Recherche Cliinique and Medtronic during the study; honoraria for lectures from Medtronic, UCB, TEVA, and Zambon; consulting fees from UCB and Zambon; and research grants from UCB, France Parkinson, and the French National Agency for Research. FM received support from the Cologne Fortune Program and the German Parkinson's Disease Foundation. FD was reimbursed congress fees and travel expenses to participate in scientific meetings from Medtronic during the study. MS reports grants from the French Programme Hospitalier de Recherche Clinique National, the German Ministry of Research Klinische Studien, and Medtronic during the study; grants from Medtronic, Boston Scientific, and Actelion; and personal fees from Merz Pharma, Zambon, Medtronic, Aleva, Boston Scientific, and Allergan. GD reports grants from the German Ministry of Research Klinische Studien, the French Programme Hospitalier de Recherche Clinique National, and Medtronic during the study; personal fees from Almirall, Novartis, and Boston Scientific; and has a patent with Thieme Publishers with royalties paid. AK has sat on an advisory board for Medtronic USA; has received honoraria for speaking from Allergan, Boehringer Ingelheim, Ipsen Pharma, Lundbeck, Medtronic, Merck, Merz Pharmaceuticals, Orion, St Jude, and UCB; and has received grants from the German Research Council and the German Ministry of Education and Research. LTo is a statistician employee of Medtronic. PK reports grants and reimbursement of congress and travel fees from Medtronic during the study; grants from the French Programme Hospitalier de Recherche Clinique National during the study; grants and personal fees from Medtronic, Boston Scientific, the Movement Disorder Society, and UCB; grants from St Jude Medical France, Edmond J & Lily Safra Foundation, the French Ministry of Health, INSERM (French National Institute of Health and Research in Medicine), France Parkinson, Swiss National Science Foundation, Roger De Spoelberch Foundation, Centre National Recherche Scientifique, Orkyn, and Homeperf; and personal fees from the European Society for Stereotactic and Functional Neurosurgery. SC reports speaker fees and reimbursement of travel and congress feesfrom Medtronic and Boston Scientific. J-MR has received honoraria for speaking engagements from and has been reimbursed congress fees and travel expenses to participate in scientific meetings by Medtronic. LTi declares grants, honoraria, and travel fees from Medtronic during the study; is an advisory board member for Medtronic, Boston Scientific, TEVA, UCB, and Archimedes Pharma; has received consultancy fees from Medtronic, Boston Scientific, Sapiens, St Jude Medical, Bayer Healthcare, UCB, and Archimedes Pharma; has received grants from the German Research Foundation, German Ministry of Research, German Parkinson Foundation, Manfred and Ursula Mueller Founation, Klueh Foundation, Hoffnungsbaum eV, NBIA Disorders Foundation, Cologne Fortune Program, Medtronic, TEVA, UCB, Boston Scientific, Archimedes, Abbott/Abbvie, Bayer, and Zur Rose Pharma; and has received payment for lectures from TEVA, Lundbeck, Bracco, Gianni PR, Medas, UCB, Deistin, Boehringer, GSK, Eumecom, Orion Pharma, Cephalon, Abbott/Abbvie, GE Medical, Archimedes, and Bayer. VC, MM, ASa, SE, JR, TDH, TW, and CS-B declare no competing interests.
Funding Information:
We acknowledge the substantial contribution of Val Stoker (Senior Principal Clinical Trial Leader, Medtronic) to the organisation of the EARLYSTIM study and the current substudy; and the study's steering committee gratefully acknowledges the substantial contribution of Yves Agid. The EARLYSTIM study was funded by the German Ministry of Research (Klinische Studien 01KG0502), the French Programme Hospitalier de Recherche Clinique National (P050909), and Medtronic.
Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/3
Y1 - 2018/3
N2 - Background: Although subthalamic stimulation is a recognised treatment for motor complications in Parkinson's disease, reports on behavioural outcomes are controversial, which represents a major challenge when counselling candidates for subthalamic stimulation. We aimed to assess changes in behaviour in patients with Parkinson's disease receiving combined treatment with subthalamic stimulation and medical therapy over a 2-year follow-up period as compared with the behavioural evolution under medical therapy alone. Methods: We did a parallel, open-label study (EARLYSTIM) at 17 surgical centres in France (n=8) and Germany (n=9). We recruited patients with Parkinson's disease who were disabled by early motor complications. Participants were randomly allocated (1:1) to either medical therapy alone or bilateral subthalamic stimulation plus medical therapy. The primary outcome was mean change in quality of life from baseline to 2 years. A secondary analysis was also done to assess behavioural outcomes. We used the Ardouin Scale of Behavior in Parkinson's Disease to assess changes in behaviour between baseline and 2-year follow-up. Apathy was also measured using the Starkstein Apathy Scale, and depression was assessed with the Beck Depression Inventory. The secondary analysis was done in all patients recruited. We used a generalised estimating equations (GEE) regression model for individual items and mixed model regression for subscores of the Ardouin scale and the apathy and depression scales. This trial is registered with ClinicalTrials.gov, number NCT00354133. The primary analysis has been reported elsewhere; this report presents the secondary analysis only. Findings: Between July, 2006, and November, 2009, 251 participants were recruited, of whom 127 were allocated medical therapy alone and 124 were assigned bilateral subthalamic stimulation plus medical therapy. At 2-year follow-up, the levodopa-equivalent dose was reduced by 39% (–363·3 mg/day [SE 41·8]) in individuals allocated bilateral subthalamic stimulation plus medical therapy and was increased by 21% (245·8 mg/day [40·4]) in those assigned medical therapy alone (p<0·0001). Neuropsychiatric fluctuations decreased with bilateral subthalamic stimulation plus medical therapy during 2-year follow-up (mean change −0·65 points [SE 0·15]) and did not change with medical therapy alone (–0·02 points [0·15]); the between-group difference in change from baseline was significant (p=0·0028). At 2 years, the Ardouin scale subscore for hyperdopaminergic behavioural disorders had decreased with bilateral subthalamic stimulation plus medical therapy (mean change −1·26 points [SE 0·35]) and had increased with medical therapy alone (1·12 points [0·35]); the between-group difference was significant (p<0·0001). Mean change from baseline at 2 years in the Ardouin scale subscore for hypodopaminergic behavioural disorders, the Starkstein Apathy Scale score, and the Beck Depression Inventory score did not differ between treatment groups. Antidepressants were stopped in 12 patients assigned bilateral subthalamic stimulation plus medical therapy versus four patients allocated medical therapy alone. Neuroleptics were started in nine patients assigned medical therapy alone versus one patient allocated bilateral subthalamic stimulation plus medical therapy. During the 2-year follow-up, two individuals assigned bilateral subthalamic stimulation plus medical therapy and one patient allocated medical therapy alone died by suicide. Interpretation: In a large cohort with Parkinson's disease and early motor complications, better overall behavioural outcomes were noted with bilateral subthalamic stimulation plus medical therapy compared with medical therapy alone. The presence of hyperdopaminergic behaviours and neuropsychiatric fluctuations can be judged additional arguments in favour of subthalamic stimulation if surgery is considered for disabling motor complications. Funding: German Federal Ministry of Education and Research, French Programme Hospitalier de Recherche Clinique National, and Medtronic.
AB - Background: Although subthalamic stimulation is a recognised treatment for motor complications in Parkinson's disease, reports on behavioural outcomes are controversial, which represents a major challenge when counselling candidates for subthalamic stimulation. We aimed to assess changes in behaviour in patients with Parkinson's disease receiving combined treatment with subthalamic stimulation and medical therapy over a 2-year follow-up period as compared with the behavioural evolution under medical therapy alone. Methods: We did a parallel, open-label study (EARLYSTIM) at 17 surgical centres in France (n=8) and Germany (n=9). We recruited patients with Parkinson's disease who were disabled by early motor complications. Participants were randomly allocated (1:1) to either medical therapy alone or bilateral subthalamic stimulation plus medical therapy. The primary outcome was mean change in quality of life from baseline to 2 years. A secondary analysis was also done to assess behavioural outcomes. We used the Ardouin Scale of Behavior in Parkinson's Disease to assess changes in behaviour between baseline and 2-year follow-up. Apathy was also measured using the Starkstein Apathy Scale, and depression was assessed with the Beck Depression Inventory. The secondary analysis was done in all patients recruited. We used a generalised estimating equations (GEE) regression model for individual items and mixed model regression for subscores of the Ardouin scale and the apathy and depression scales. This trial is registered with ClinicalTrials.gov, number NCT00354133. The primary analysis has been reported elsewhere; this report presents the secondary analysis only. Findings: Between July, 2006, and November, 2009, 251 participants were recruited, of whom 127 were allocated medical therapy alone and 124 were assigned bilateral subthalamic stimulation plus medical therapy. At 2-year follow-up, the levodopa-equivalent dose was reduced by 39% (–363·3 mg/day [SE 41·8]) in individuals allocated bilateral subthalamic stimulation plus medical therapy and was increased by 21% (245·8 mg/day [40·4]) in those assigned medical therapy alone (p<0·0001). Neuropsychiatric fluctuations decreased with bilateral subthalamic stimulation plus medical therapy during 2-year follow-up (mean change −0·65 points [SE 0·15]) and did not change with medical therapy alone (–0·02 points [0·15]); the between-group difference in change from baseline was significant (p=0·0028). At 2 years, the Ardouin scale subscore for hyperdopaminergic behavioural disorders had decreased with bilateral subthalamic stimulation plus medical therapy (mean change −1·26 points [SE 0·35]) and had increased with medical therapy alone (1·12 points [0·35]); the between-group difference was significant (p<0·0001). Mean change from baseline at 2 years in the Ardouin scale subscore for hypodopaminergic behavioural disorders, the Starkstein Apathy Scale score, and the Beck Depression Inventory score did not differ between treatment groups. Antidepressants were stopped in 12 patients assigned bilateral subthalamic stimulation plus medical therapy versus four patients allocated medical therapy alone. Neuroleptics were started in nine patients assigned medical therapy alone versus one patient allocated bilateral subthalamic stimulation plus medical therapy. During the 2-year follow-up, two individuals assigned bilateral subthalamic stimulation plus medical therapy and one patient allocated medical therapy alone died by suicide. Interpretation: In a large cohort with Parkinson's disease and early motor complications, better overall behavioural outcomes were noted with bilateral subthalamic stimulation plus medical therapy compared with medical therapy alone. The presence of hyperdopaminergic behaviours and neuropsychiatric fluctuations can be judged additional arguments in favour of subthalamic stimulation if surgery is considered for disabling motor complications. Funding: German Federal Ministry of Education and Research, French Programme Hospitalier de Recherche Clinique National, and Medtronic.
UR - http://www.scopus.com/inward/record.url?scp=85042013689&partnerID=8YFLogxK
U2 - 10.1016/S1474-4422(18)30035-8
DO - 10.1016/S1474-4422(18)30035-8
M3 - Article
C2 - 29452685
AN - SCOPUS:85042013689
SN - 1474-4422
VL - 17
SP - 223
EP - 231
JO - The Lancet Neurology
JF - The Lancet Neurology
IS - 3
ER -