Does Gabapentin and Lamotriginel Have Significantly Fewer Side-Effects While Providing Equal or Better Seizure Control Than the Current Drug Choice, Carbamazepine, for the Treatment of Seizures in the Elderly.

Condition(s) targeted: Seizures

Intervention: Carbamazepine (Drug); Gabapentin (Drug); Lamotrigine (Drug)

Phase: Phase 3

Status: Completed

Sponsored by: Department of Veterans Affairs

New onset epilepsy in the elderly occurs in 45,000-50,000 elderly patients each year. These patients are especially vulnerable to side effects from medications because of changes caused by the aging process and the fact that these patients often have many common diseases for which they are already receiving medications for so that the likelihood of drug interactions is increased. Two new drugs, gabapentin and lamotrigine, have recently been approved by the FDA as antiepileptic drugs. These drugs have demonstrated efficacy in the treatment of partial onset seizures, the most common seizures in the elderly. These new compounds also have favorable side effect profiles and infrequent drug-drug interactions and, therefore, would be expected to be well-tolerated in the elderly.

Official title: CSP #428 - Treatment of Seizures in the Elderly Population

Study design: Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study

Detailed description: Primary Hypothesis: The primary hypothesis for this study is that one or both of two newly FDA approved antiepileptic drugs, gabapentin and lamotrigine, will have significantly fewer side-effects while providing equal or possibly better seizure control than the current world-wide drug of choice, carbamazepine, for the treatment of seizures in the elderly.

Secondary Hypotheses: Secondary aims of the study are to determine which of the three drugs being studied (1) has the fewest side-effects, (2) produces the best seizure control, (3) has the least impairment of cognitive function, (4) has the best effect on mood and (5) has the best effect on quality of life.

Intervention: Patients are randomized to carbamazepine, gabapentin or lamotrigine. Target doses are 600mg for carbamazepine (200mg tablets overencapsulated), 1500mg for gabapentin (300mg capsules), and 150mg for lamotrigine (25mg tablets). Carbamazepine and gabapentin patients also receive a placebo tablet while lamotrigine patients also receive a placebo capsule.

Primary Outcomes: The primary outcome measure is retention in the study at 12 months. Major secondary outcomes are seizure frequency during first 12 months, time to first seizure, total scores from Systemic Toxicity and Neurotoxicity Rating Scales, the Mattis Dementia Rating Scale (cognitive function), Hamilton Depression Scale (mood) and SF-36 Health Survey (quality of life).

Study Abstract: New onset epilepsy in the elderly occurs in 45,000-50,000 elderly patients each year. These patients are especially vulnerable to side effects from medications because of changes caused by the aging process and the fact that these patients often have many common diseases for which they are already receiving medications for so that the likelihood of drug interactions is increased. Two new drugs, gabapentin and lamotrigine, have recently been approved by the FDA as antiepileptic drugs. These drugs have demonstrated efficacy in the treatment of partial onset seizures, the most common seizures in the elderly. These new compounds also have favorable side effect profiles and infrequent drug-drug interactions and, therefore, would be expected to be well-tolerated in the elderly. Thus, the primary objective of this study is to evaluate the tolerability and efficacy of these two new antiepileptic drugs individually compared to a standard antiepileptic drug, carbamazepine, in an elderly population (>60 years of age) with new onset, unprovoked epileptic seizures.

The study is a 63-month, randomized, double-blind trial of three antiepileptic drugs: carbamazepine, gabapentin, and lamotrigine. Patient recruitment occured during the first 51 months with each patient being followed for at least one year. There were 593 patients enrolled from 18 VA medical centers. Patients are veterans 60 years of age or older who have new onset, unprovoked seizures of focal onset, with or without secondary generalization. Patients with seizures secondary to toxic-metabolic causes, acute medical or neurological conditions or progressive diseases of the brain such as brain tumors are excluded. A double-dummy design is being employed to preserve the blind. Target doses for the study medications are: carbamazepine-600 mg., gabapentin-1500 mg., and lamotrigine-150 mg. Patients are assessed biweekly during the first 8 weeks, every 4 weeks until week 24 and every 8 weeks until week 52. Patients wishing to continue on their study drug after 52 weeks are seen quarterly for an additional year.

RESULTS: For the primary outcome measure of retention at 12 months, there was a statistically significant (p=0. 0002) overall difference between the treatment groups (lamotrigine=55. 8%, gabapentin=49. 0%, and carbamazepine=35. 5%). The paired comparisons indicated significant differences between lamotrigine and carbamazepine (p<0. 0001) and gabapentin and carbamazepine (p=0. 008). Consideration of reasons for early terminations indicates significant overall differences (p=0. 001) between treatment groups for early terminations due to adverse events (lamotrigine=12. 1%, gabapentin=21. 6%, and carbamazepine=31. 0%. There were significant paired comparisons for lamotrigine vs carbamazepine (p<0. 0001) and lamotrigine vs gabapentin (p=0. 015). There were no differences between the treatment groups for percent of patients seizure free at 3, 6, and 12 months or for the time to first, second, fifth, or tenth seizure (all p>0. 05). When individual adverse events during the first 12 months on study drug were considered, it was seen that more gabapentin patients had significantly more weight gain, severe weight gain (>18 pounds), and water retention than patients on either lamotrigine or carbamazepine. Hypersensitivity (rash of any degree) occurred more frequently with carbamazpine than with lamotrigine (p=0. 007). The overall conclusion is that lamotrigine and gabapentin should be considered as initial therapy for older patients with newly diagnosed seizures.

Rowan, A. J., Ramsay, R. E., Collins, J. F., Pryor, F., Boardman, K. D., Uthman, B. M., Spitz, M., Frederick, T., Towne, A., Carter, G. S., Marks, W., Felicetta, J., Tomyanovich, M. L., and the

VA Cooperative Study 428 Group - New onset geriatric epilepsy. A randomized study of

gabapentin, lamotrigine, and carbamazepine. Neurology 64 1868-1873, 2005

Minimum age: 60 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Veterans 60 years of age or older who have new onset, unprovoked seizures of focal onset, with or without secondary generalization.

Birmingham VA Medical Center, Birmingham, Alabama 35233, United States

Carl T. Hayden VA Medical Center, Phoenix, Arizona 85012, United States

San Francisco VAMC, San Francisco, California 94121, United States

Vamc - San Diego, San Diego, Ca, SAN DIEGO, California 92161, United States

Vamc - West Los Angeles, Los Angeles, Ca, Los Angeles, California 90073, United States

Denver VA Medical Center, Denver, Colorado 80220, United States

Study Chairperson, Miami, Florida 33125, United States

Gainesville VA Medical Center, Gainesville, Florida 32608-1197, United States

Miami VA Medical Center, Miami, Florida 33125, United States

Vamc - Bay Pines, Fl, Bay Pines, Florida 33744, United States

Edward Hines Jr. VA Hospital, Hines, Illinois 60141, United States

Chicago VA Medical Center (West Side), Chicago, Illinois 60612, United States

New Orleans VAMC, New Orleans, Louisiana 70112, United States

Boston VA Medical Center, Boston, Massachusetts 02130, United States

Study Chairman, Bronx, New York 10468, United States

Bronx VA Medical Center, Bronx, New York 10468, United States

Oklahoma City VA Medical Center, Oklahoma City, Oklahoma 73104, United States

Vamc - Pittsburgh, Pittsburgh, Pa, Pittsburgh, Pennsylvania 15240-1001, United States

Dallas VA Medical Center, Dallas, Texas 75216, United States

Hunter Holmes McGuire VA Medical Center, Richmond, Virginia 23249, United States

Starting date: January 1998
Ending date: March 2003
Last updated: February 2, 2007