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Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy PowerPoint Presentation

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Slide 1-

SANTE: Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy Professor Ley Sander MD PhD FRCP
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2 Current Treatments for Epilepsy Antiepileptic Drugs Up to 70% seizure-free Epilepsy Surgery Up to 10% of people with chronic epilepsy Curative Palliative Ketogenic diet Very selected patients usually with severe childhood epilepsies Vagus Nerve Stimulation (VNS) Palliative Other treatments Biofeedback Light therapy Avoidance therapy Alternative and complementary therapies
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DBS Therapy for Epilepsy Deep Brain Stimulation (DBS) uses an implantable neurostimulator to deliver electrical stimulation to the anterior nucleus of the thalamus (ANT) of the brain, on each side Implanted in the brain
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4 Rationale for ANT Stimulation The ANT is a reasonable stimulation site based on: Anatomical function of this nucleus in a well known brain circuit (Papez), implicated to be involved in seizures. Stimulation of ANT evokes potentials, reduces synchrony, and increases inhibition in hippocampus or neocortex. ANT stimulation was independently assessed in 6 pilot studies in subjects with refractory epilepsy.
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5 Deep Brain Stimulation (DBS) Therapies DBS is an approved therapy for several other conditions Since 1995, more than 75,000 patients worldwide have received DBS therapy. Tremor PD Dystonia OCD Pilot patients IDE 1st implant PMA/S Pre-PMAMtg Epilepsy
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6 Medtronic DBS System for Epilepsy Implantable neurostimulator Leads Extensions Implantable components Clinician programmer Patient programmer Programmers
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7 SANTE Study Design Visits Blinded Phase (3 mo) Unblinded Phase (9 mo) Long-Term Follow-up Phase (visits every 6 mo & monthly phone calls) Op Phase (1 mo) Baseline Phase (3 mo) Wk -12 Wk -8 Wk -4 Wk 0 Mo 1 Mo 2 Mo 3 Mo 4 Mo 5 Mo 6 Mo 7 Mo 8 Mo 9 Mo 10 Mo 11 Mo 12 Yr 1 / / / / Yr 2 Yr 3 No restrictions on programming Restricted programming changes (↑ 7.5V or↑185 pps) Randomization Implant Control ↑5V Primary efficacy analysis Stim turned ON Active 5V Control 0V 145 pps 90 us 1 m ON, 5 m OFF
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8 Objectives Primary Efficacy (Blinded Phase) To demonstrate that the reduction in seizure rate in the active group is greater than in the control group Secondary (Blinded Phase) Responder rate Seizure free days and seizure free intervals Treatment failures Additional Study Measures (Blinded Phase) Seizure type and severity Quality of life (QOLIE) Neuropsychological testing Therapy access controller activations Healthcare resource utilization Rescue medication use Safety Characterize adverse events Characterize incidence of Sudden Unexplained Death in Epilepsy (SUDEP)
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9 Eligibility Criteria Age 18-65, inclusive 6 or more PS with or without secondary generalization per month No more than 30 days between seizures in the baseline phase Refractory to at least 3 AEDs, currently taking 1-4 AEDs Not a candidate for, or unwilling to undergo, potentially curative resective surgery IQ ≥ 70 If VNS in place, willing to remove it prior to or at time of DBS implantation
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10 Demographics
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11 Accountability 157 enrolled 148 started Baseline 110 implanted 109 randomized into Blinded Phase 108 started Unblinded Phase 105 started LTFU 102 completed 2 years 57 completed 3 years 91 remain active in study 1 skipped to LTFU 1 skipped to LTFU 9 discontinued 38 discontinued 5 discontinued 3 discontinued 3 discontinued 8 discontinued 42 have not yet reached 3 yrs
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12 Discontinuations
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13 Blinded Phase: Efficacy Results Blinded Phase (3 mo) Unblinded Phase (9 mo) Long-Term Follow-up Phase (visits every 6 mo & monthly phone calls) Op Phase (1 mo) Baseline Phase (3 mo) Wk -12 Mo 1 Mo 2 Mo 3 Mo 4 Yr 1 / / / / Yr 2 Yr 3 Randomization Implant Wk 0
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14 Median Total Seizure Frequency Reduction Both groups had a similar drop in the Operative Phase The active group continues to improve while the control group trends towards baseline
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15 Seizure Reduction by Seizure Type
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16 Epilepsy-Related Injuries Persons with epilepsy are at a higher risk for incurring seizure-related accidental injurya a Beghi et al, Epilepsia, 2002
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17 Blinded Phase Efficacy Results Summary A statistically significant reduction in the seizure rate was seen in the Active group compared to the Control group. 40% reduction in seizures is clinically meaningful in this population. Complex partial, “most severe,” and seizure related injuries were significantly less with stimulation. All analyses found a significant benefit for the active intervention in the final month of the Blinded Phase. These results provide a reasonable assurance of effectiveness.
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18 Unblinded Phase Blinded Phase (3 mo) Unblinded Phase (9 mo) Long-Term Follow-up Phase (visits every 6 mo & monthly phone calls) Op Phase (1 mo) Baseline Phase (3 mo) Wk -12 Mo 1 Mo 2 Mo 3 Mo 4 Mo 5 Mo 6 Mo 7 Mo 8 Mo 9 Mo 10 Mo 11 Mo 12 Yr 1 / / / / Yr 2 Yr 3 Control subjects ↑5V Randomization Implant Wk 0
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19 Seizure Frequency Change at 2 Yrs (by Subject) Question to panel #3
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20 Responder Rate ( ≥ 50% reduction in total seizures) Question to panel #13
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21 Quality of Life in Epilepsy-31
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22 Patient Satisfaction with the Therapy Rate your overall satisfaction with the therapy (0-4 scale) 74% reported being satisfied or greatly satisfied with the results of their therapy. Considering your overall outcome with your therapy, and considering the operation(s), hospitalization(s), discomfort and expense involved, would you go through it all again for the same result? 81% reported that they would go through the therapy again knowing the result. Based on your experience, would you recommend this therapy to a friend with epilepsy similar to yours? 88% would recommend it to a friend. At one year post randomization
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23 Efficacy Summary Blinded Phase A statistically significant reduction in the seizure rate was seen in the Active group compared to the Control group. 40% seizure reduction is clinically meaningful in this population Complex partial, “most severe,” and seizure related injuries were significantly less with stimulation. Efficacy is maintained long term 41%, 56%, 68% seizure reduction at 1, 2, 3 years Quality of life and responder rate improve long-term 13% of subjects were seizure-free for at least 6 months DBS therapy is efficacious in this patient population
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Most Frequent Serious Adverse Events Leads not in target Criteria for randomization included at least one lead contact within the target ANT 8.2% (9/110) subjects required lead revision 14/220 (6.4%) of leads Rate similar to DBS for other movement disorders All leads were successfully repositioned Implant site infection 7.3% (8/110) subjects Rate similar to DBS for other movement disorders None were in the brain 5 required partial or complete explant, 2 re-implanted 24
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Safety Summary Depression and memory impairment reported more frequently in Active group patients Depression monitoring Stable neuropsychological testing profile Seizures may occur upon initiation of stimulation No device-related deaths and SUDEP rate lower than that reported in a similar population Procedural and hardware-related risks consistent with other DBS therapies 25
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26 Conclusion Refractory epilepsy is highly prevalent; new therapies are needed Benefit of DBS was shown in some people with a long history of epilepsy who had failed most other treatments Safety profile of DBS acceptable compared to the significant consequences of continued seizures Fisher et al. Epilepsia; 2010