Greater Response to Placebo in Children Than in Adults: A Systematic Review and Meta-Analysis in Drug-Resistant Partial Epilepsy
Background:
Despite guidelines establishing the need to perform comprehensive paediatric drug development programs, pivotal trials in children with epilepsy have been completed mostly in Phase IV as a postapproval replication of adult data. However, it has been shown that the treatment response in children can differ from that in adults. It has not been investigated whether differences in drug effect between adults and children might occur in the treatment of drug-resistant partial epilepsy, although such differences may have a substantial impact on the design and results of paediatric randomised controlled trials (RCTs).
Methods and Findings:
Three electronic databases were searched for RCTs investigating any antiepileptic drug (AED) in the add-on treatment of drug-resistant partial epilepsy in both children and adults. The treatment effect was compared between the two age groups using the ratio of the relative risk (RR) of the 50% responder rate between active AEDs treatment and placebo groups, as well as meta-regression. Differences in the response to placebo and to active treatment were searched using logistic regression. A comparable approach was used for analysing secondary endpoints, including seizure-free rate, total and adverse events-related withdrawal rates, and withdrawal rate for seizure aggravation. Five AEDs were evaluated in both adults and children with drug-resistant partial epilepsy in 32 RCTs. The treatment effect was significantly lower in children than in adults (RR ratio: 0.67 [95% confidence interval (CI) 0.51–0.89]; p = 0.02 by meta-regression). This difference was related to an age-dependent variation in the response to placebo, with a higher rate in children than in adults (19% versus 9.9%, p < 0.001), whereas no significant difference was observed in the response to active treatment (37.2% versus 30.4%, p = 0.364). The relative risk of the total withdrawal rate was also significantly lower in children than in adults (RR ratio: 0.65 [95% CI 0.43–0.98], p = 0.004 by metaregression), due to higher withdrawal rate for seizure aggravation in children (5.6%) than in adults (0.7%) receiving placebo (p < 0.001). Finally, there was no significant difference in the seizure-free rate between adult and paediatric studies.
Conclusions:
Children with drug-resistant partial epilepsy receiving placebo in double-blind RCTs demonstrated significantly greater 50% responder rate than adults, probably reflecting increased placebo and regression to the mean effects. Paediatric clinical trial designs should account for these age-dependent variations of the response to placebo to reduce the risk of an underestimated sample size that could result in falsely negative trials.
Vyšlo v časopise:
Greater Response to Placebo in Children Than in Adults: A Systematic Review and Meta-Analysis in Drug-Resistant Partial Epilepsy. PLoS Med 5(8): e166. doi:10.1371/journal.pmed.0050166
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pmed.0050166
Souhrn
Background:
Despite guidelines establishing the need to perform comprehensive paediatric drug development programs, pivotal trials in children with epilepsy have been completed mostly in Phase IV as a postapproval replication of adult data. However, it has been shown that the treatment response in children can differ from that in adults. It has not been investigated whether differences in drug effect between adults and children might occur in the treatment of drug-resistant partial epilepsy, although such differences may have a substantial impact on the design and results of paediatric randomised controlled trials (RCTs).
Methods and Findings:
Three electronic databases were searched for RCTs investigating any antiepileptic drug (AED) in the add-on treatment of drug-resistant partial epilepsy in both children and adults. The treatment effect was compared between the two age groups using the ratio of the relative risk (RR) of the 50% responder rate between active AEDs treatment and placebo groups, as well as meta-regression. Differences in the response to placebo and to active treatment were searched using logistic regression. A comparable approach was used for analysing secondary endpoints, including seizure-free rate, total and adverse events-related withdrawal rates, and withdrawal rate for seizure aggravation. Five AEDs were evaluated in both adults and children with drug-resistant partial epilepsy in 32 RCTs. The treatment effect was significantly lower in children than in adults (RR ratio: 0.67 [95% confidence interval (CI) 0.51–0.89]; p = 0.02 by meta-regression). This difference was related to an age-dependent variation in the response to placebo, with a higher rate in children than in adults (19% versus 9.9%, p < 0.001), whereas no significant difference was observed in the response to active treatment (37.2% versus 30.4%, p = 0.364). The relative risk of the total withdrawal rate was also significantly lower in children than in adults (RR ratio: 0.65 [95% CI 0.43–0.98], p = 0.004 by metaregression), due to higher withdrawal rate for seizure aggravation in children (5.6%) than in adults (0.7%) receiving placebo (p < 0.001). Finally, there was no significant difference in the seizure-free rate between adult and paediatric studies.
Conclusions:
Children with drug-resistant partial epilepsy receiving placebo in double-blind RCTs demonstrated significantly greater 50% responder rate than adults, probably reflecting increased placebo and regression to the mean effects. Paediatric clinical trial designs should account for these age-dependent variations of the response to placebo to reduce the risk of an underestimated sample size that could result in falsely negative trials.
Zdroje
1. GuerriniR
2006
Epilepsy in children.
Lancet
367
499
524
2. GarofaloE
2006
Obtaining pediatric indications for new anti-epileptic drugs: how and when.
Epilepsy Res
68
38
42
3. SchmidtB
2007
Clinical development of antiepileptic drugs in adults.
Neurotherapeutics
4
62
69
4. CaldwellPHMurphySBButowPNCraigJC
2004
Clinical trials in children.
Lancet
364
803
811
5. PellockJM
1998
Pediatric trials: practical issues. Special populations and trial design.
Adv Neurol
76
167
171
6. SteinbrookR
2002
Testing medications in children.
N Engl J Med
347
1462
1470
7. PeruccaE
2006
Clinical pharmacokinetics of new-generation antiepileptic drugs at the extremes of age.
Clin Pharmacokinet
45
351
363
8. ShinnarSPellockJM
2005
The trials and tribulations of pediatric drug trials.
Neurology
65
1348
1349
9. SandlerA
2005
Placebo effects in developmental disabilities: implications for research and practice.
Ment Retard Dev Disabil Res Rev
11
164
170
10. FernandesRFerreiraJJSampaioC
2008
The placebo response in studies of acute migraine.
J Pediatr
152
527
33
533.e.l
11. LewisDWWinnerPWasiewskiW
2005
The placebo responder rate in children and adolescents.
Headache
45
232
239
12. RothnerADWasiewskiWWinnerPLewisDStankowskiJ
2006
Zolmitriptan oral tablet in migraine treatment: high placebo responses in adolescents.
Headache
46
101
109
13. [No authors listed]
1993
Efficacy of felbamate in childhood epileptic encephalopathy (Lennox-Gastaut syndrome). The Felbamate Study Group in Lennox-Gastaut Syndrome.
N Engl J Med
328
29
33
14. BeranRGBerkovicSFDunaganFMVajdaFJDantaG
1998
Double-blind, placebo-controlled, crossover study of lamotrigine in treatment-resistant generalised epilepsy.
Epilepsia
39
1329
1333
15. BerkovicSFKnowltonRCLeroyRFSchiemannJFalterU
2007
Placebo-controlled study of levetiracetam in idiopathic generalized epilepsy.
Neurology
69
1751
1760
16. BitonVMontourisGDRitterFRivielloJJReifeR
1999
A randomized, placebo-controlled study of topiramate in primary generalized tonic-clonic seizures. Topiramate YTC Study Group.
Neurology
52
1330
1337
17. BitonVSackellaresJCVuongAHammerAEBarrettPS
2005
Double-blind, placebo-controlled study of lamotrigine in primary generalized tonic-clonic seizures.
Neurology
65
1737
1743
18. ChadwickDLeidermanDBSauermannWAlexanderJGarofaloE
1996
Gabapentin in generalized seizures.
Epilepsy Res
25
191
197
19. GlauserTKlugerGSachdeoRKraussGPerdomoC
2008
Rufinamide for generalized seizures associated with Lennox-Gastaut syndrome.
Neurology
17
1950
1958
20. MotteJTrevathanEArvidssonJFBarreraMNMullensEL
1997
Lamotrigine for generalized seizures associated with the Lennox-Gastaut syndrome. Lamictal Lennox-Gastaut Study Group.
N Engl J Med
337
1807
1812
21. SachdeoRCGlauserTARitterFReifeRLimP
1999
A double-blind, randomized trial of topiramate in Lennox-Gastaut syndrome. Topiramate YL Study Group.
Neurology
52
1882
1887
22. [No authors listed]
1989
Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy.
Epilepsia
30
389
399
23. FrenchJAKannerAMBautistaJAbou-KhalilBBrowneT
2004
Efficacy and tolerability of the new antiepileptic drugs II: treatment of refractory epilepsy: report of the Therapeutics and Technology Assessment Subcommittee and Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society.
Neurology
62
1261
1273
24. GumnitRJWalczakTS
2001
Guidelines for essential services, personnel, and facilities in specialized epilepsy centers in the United States.
Epilepsia
42
804
814
25. PerrucaE
1998
Pharmacoresistance in epilepsy: how should it be defined.
CNS Drugs
10
171
179
26. RegestaGTanganelliP
1999
Clinical aspects and biological bases of drug-resistant epilepsies.
Epilepsy Res
34
109
122
27. European Medicines Agency
2001
International Conference on Harmonisation.
ICH topic E11 clinical investigation of medicinal products in the paediatric population
Available: http://www.emea.eu/pdfs/human/ich/271199EN.pdf. Accessed 07 July 2008.
28. JadadARMooreRACarrollDJenkinsonCReynoldsDJ
1996
Assessing the quality of reports of randomized clinical trials: is blinding necessary.
Control Clin Trials
17
1
12
29. GazzolaDMBalcerLJFrenchJA
2007
Seizure-free outcome in randomized add-on trials of the new antiepileptic drugs.
Epilepsia
48
1303
1307
30. HigginsJPThompsonSG
2002
Quantifying heterogeneity in a meta-analysis.
Stat Med
21
1539
1558
31. CucheratM
2000
EasyMA Sofware Version 2000
Available: http://www.spc.univ-lyon1.fr/easyma.net/. Accessed 07 July 08.
32. CucheratMBoisselJPLeizoroviczAHaughMC
1997
EasyMA: a program for the meta-analysis of clinical trials.
Comput Methods Programs Biomed
53
187
190
33. RosenfeldWAbou-KhalilBReifeRHegadusRPledgerG
1996
Placebo-controlled trial of topiramate as adjunctive therapy to carbamazepine or phenitoine for partial onset seizures.
Epilepsia
37
153
34. SchmidtDRiedRSRappP
1993
Add-on treatment with Lamotrigine for intractable partial epilepsy: a placebo-controlled, cross-over trial.
Epilepsia
34
66
35. JetteNJMarsonAGHuttonJL
2002
Topiramate add-on for drug-resistant partial epilepsy.
Cochrane Database Syst Rev CD001417
Available: http://www.cochrane.org/reviews/en/ab001417.html. Accessed 07 July 08.
36. RamaratnamSMarsonAGBakerGA
2001
Lamotrigine add-on for drug-resistant partial epilepsy.
Cochrane Database Syst Rev CD001909
Available: http://www.cochrane.org/reviews/en/ab001909.html. Accessed 07 July 08.
37. DuchownyMPellockJMGrafWDBillardCGilmanJ
1999
A placebo-controlled trial of lamotrigine add-on therapy for partial seizures in children. Lamictal Pediatric Partial Seizure Study Group.
Neurology
53
1724
1731
38. Huedo-MedinaTBSanchez-MecaFMarin-MartinezFBotellaJ
2006
Assessing heterogenity in meta-analysi: Q statistic or I2 index.
Psychol Methods
11
193
206
39. IoannidisJPatsopoulosNEvangelouE
2007
Uncertainty in heterogeneity estimates in meta-analyses.
BMJ
335
914
916
40. HoppeCPoepelAElgerCE
2007
Epilepsy: accuracy of patient seizure counts.
Arch Neurol
64
1595
1599
41. KerlingFMuellerSPauliEStefanH
2006
When do patients forget their seizures? An electroclinical study.
Epilepsy Behav
9
281
285
42. CastilloSSchmidtDBWhiteS
2000
Oxcarbazepine add-on for drug-resistant partial epilepsy.
Cochrane Database Syst Rev CD002028
Available: http://www.cochrane.org/reviews/en/ab002028.html. Accessed 07 July 08.
43. ChadwickDWMarsonAG
2005
Zonisamide add-on for drug-resistant partial epilepsy.
Cochrane Database Syst Rev CD001416
Available: http://www.cochrane.org/reviews/en/ab001416.html. Accessed 07 July 08.
44. ChaisewikulRPriviteraMDHuttonJLMarsonAG
2001
Levetiracetam add-on for drug-resistant localization related (partial) epilepsy.
Cochrane Database Syst Rev CD001901
http://www.cochrane.org/reviews/en/ab001901.html. Accessed 07 July 08.
45. LeachJPMarsonAGHuttonJL
2002
Remacemide for drug-resistant localization related epilepsy.
Cochrane Database Syst Rev CD001900
Available: http://www.cochrane.org/reviews/en/ab001900.html. Accessed 07 July 08.
46. LozsadiDHemmingKMarsonA
2008
Pregabalin add-on for drug-resistant partial epilepsy.
Cochrane Database Syst Rev CD005612
Available: http://www.cochrane.org/reviews/en/ab005612.html. Accessed 07 July 08.
47. MarsonAGKadirZAHuttonJLChadwickDW
2000
Gabapentin add-on for drug-resistant partial epilepsy.
Cochrane Database Syst Rev CD001415
Available: http://www.cochrane.org/reviews/en/ab001415.html. Accessed 07 July 08.
48. PereiraJMarsonAGHuttonJL
2002
Tiagabine add-on for drug-resistant partial epilepsy.
Cochrane Database Syst Rev CD001908
Available: http://www.cochrane.org/reviews/en/ab001908.html. Accessed 07 July 08.
49. MarsonAGHuttonJLLeachJPCastilloSSchmidtD
2001
Levetiracetam, oxcarbazepine, remacemide and zonisamide for drug resistant localization-related epilepsy: a systematic review.
Epilepsy Res
46
259
270
50. MarsonAGKadirZAHuttonJLChadwickDW
1997
The new antiepileptic drugs: a systematic review of their efficacy and tolerability.
Epilepsia
38
859
880
51. OtoulCArrigoCvan RijckevorselKFrenchJA
2005
Meta-analysis and indirect comparisons of levetiracetam with other second-generation antiepileptic drugs in partial epilepsy.
Clin Neuropharmacol
28
72
78
52. [No authors listed]
2006
Regulation (EC) No 1901/2006 of the European Parliament and of the Council of 12 December 2006 on medical products for paediatric use
Official Journal of the European Union
Available: http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-1/reg_2006_1901/reg_2006_1901_en.pdf. Accessed 07 July 08.
53. National Institutes of Health
1998
NIH policy and guidelines on the inclusion of children as participants in research involving human subjects
Available: http://grants.nih.gov/grants/guide/notice-files/not98–024.html. Accessed 07 July 08.
54. AppletonRFichtnerKLaMoreauxLAlexanderJHalsallG
1999
Gabapentin as add-on therapy in children with refractory partial seizures: a 12-week, multicentre, double-blind, placebo-controlled study. Gabapentin Paediatric Study Group.
Epilepsia
40
1147
1154
55. EltermanRDGlauserTAWyllieEReifeRWuSC
1999
A double-blind, randomized trial of topiramate as adjunctive therapy for partial-onset seizures in children. Topiramate YP Study Group.
Neurology
52
1338
1344
56. AnhutHAshmanPFeuersteinTJSauermannWSaundersM
1994
Gabapentin (Neurontin) as add-on therapy in patients with partial seizures: a double-blind, placebo-controlled study. The International Gabapentin Study Group.
Epilepsia
35
795
801
57. TassinariCAMichelucciRChauvelPChodkiewiczJShorvonS
1996
Double-blind, placebo-controlled trial of topiramate (600 mg daily) for the treatment of refractory partial epilepsy.
Epilepsia
37
763
768
58. YamauchiTKanekoSYagiKSaseS
2006
Treatment of partial seizures with gabapentin: double-blind, placebo-controlled, parallel-group study.
Psychiatry Clin Neurosci
60
507
515
59. Pina-GarzaJEEspinozaRNordliDBennettDASpiritoS
2005
Oxcarbazepine adjunctive therapy in infants and young children with partial seizures.
Neurology
65
1370
1375
60. ChironCTonnelierSReyEBrunetMLTranA
2006
Stiripentol in childhood partial epilepsy: randomized placebo-controlled trial with enrichment and withdrawal design.
J Child Neurol
21
496
502
61. ChironCDulacOGramL
1996
Vigabatrin withdrawal randomized study in children.
Epilepsy Res
25
209
215
62. ChironCDulacOPonsG
2008
Antiepileptic drug development in children: considerations for a revisited strategy.
Drugs
68
17
25
63. Pina-GarzaJELevisohnPGucuyenerKMikatiMAWarnockCR
2007
Adjunctive lamotrigine for partial seizures in patients aged 1 to 24 months.
Neurology
64. [No authors listed]
1990
Gabapentin in partial epilepsy. UK Gabapentin Study Group.
Lancet
335
1114
1117
65. SiveniusJKalviainenRYlinenARiekkinenP
1991
Double-blind study of Gabapentin in the treatment of partial seizures.
Epilepsia
32
539
542
66. [No authors listed]
1993
Gabapentin as add-on therapy in refractory partial epilepsy: a double-blind, placebo-controlled, parallel-group study. The US Gabapentin Study Group No. 5.
Neurology
43
2292
2298
67. BinnieCDDebetsRMEngelsmanMMeijerJWMeinardiH
1989
Double-blind crossover trial of lamotrigine (Lamictal) as add-on therapy in intractable epilepsy.
Epilepsy Res
4
222
229
68. JawadSRichensAGoodwinGYuenWC
1989
Controlled trial of lamotrigine (Lamictal) for refractory partial seizures.
Epilepsia
30
356
363
69. LoiseauPYuenAWDucheBMenagerTArne-BesMC
1990
A randomised double-blind placebo-controlled crossover add-on trial of lamotrigine in patients with treatment-resistant partial seizures.
Epilepsy Res
7
136
145
70. MatsuoFBergenDFaughtEMessenheimerJADrenAT
1993
Placebo-controlled study of the efficacy and safety of lamotrigine in patients with partial seizures. U.S. Lamotrigine Protocol 0.5 Clinical Trial Group.
Neurology
43
2284
2291
71. SchapelGJBeranRGVajdaFJBerkovicSFMashfordML
1993
Double-blind, placebo controlled, crossover study of lamotrigine in treatment resistant partial seizures.
J Neurol Neurosurg Psychiatry
56
448
453
72. SmithDBakerGDaviesGDeweyMChadwickDW
1993
Outcomes of add-on treatment with lamotrigine in partial epilepsy.
Epilepsia
34
312
322
73. MessenheimerJRamsayREWillmoreLJLeroyRFZielinskiJJ
1994
Lamotrigine therapy for partial seizures: a multicenter, placebo-controlled, double-blind, cross-over trial.
Epilepsia
35
113
121
74. BoasJDamMFriisMLKristensenOPedersenB
1996
Controlled trial of lamotrigine (Lamictal) for treatment-resistant partial seizures.
Acta Neurol Scand
94
247
252
75. Ben-MenachemEFalterU
2000
Efficacy and tolerability of levetiracetam 3000 mg/d in patients with refractory partial seizures: a multicenter, double-blind, responder-selected study evaluating monotherapy. European Levetiracetam Study Group.
Epilepsia
41
1276
1283
76. CereghinoJJBitonVAbou-KhalilBDreifussFGauerLJ
2000
Levetiracetam for partial seizures: results of a double-blind, randomized clinical trial.
Neurology
55
236
242
77. ShorvonSDLowenthalAJanzDBielenELoiseauP
2000
Multicenter double-blind, randomized, placebo-controlled trial of levetiracetam as add-on therapy in patients with refractory partial seizures. European Levetiracetam Study Group.
Epilepsia
41
1179
1186
78. TsaiJJYenDJHsihMSChenSSHiersemenzelR
2006
Efficacy and safety of levetiracetam (up to 2000 mg/day) in Taiwanese patients with refractory partial seizures: a multicenter, randomized, double-blind, placebo-controlled study.
Epilepsia
47
72
81
79. GlauserTAAyalaREltermanRDMitchellWGVan OrmanCB
2006
Double-blind placebo-controlled trial of adjunctive levetiracetam in pediatric partial seizures.
Neurology
66
1654
1660
80. BarcsGWalkerEBElgerCEScaramelliAStefanH
2000
Oxcarbazepine placebo-controlled, dose-ranging trial in refractory partial epilepsy.
Epilepsia
41
1597
1607
81. GlauserTANigroMSachdeoRPasterisLAWeinsteinS
2000
Adjunctive therapy with oxcarbazepine in children with partial seizures. The Oxcarbazepine Pediatric Study Group.
Neurology
54
2237
2244
82. Ben-MenachemEHenriksenODamMMikkelsenMSchmidtD
1996
Double-blind, placebo-controlled trial of topiramate as add-on therapy in patients with refractory partial seizures.
Epilepsia
37
539
543
83. FaughtEWilderBJRamsayREReifeRAKramerLD
1996
Topiramate placebo-controlled dose-ranging trial in refractory partial epilepsy using 200-, 400-, and 600-mg daily dosages. Topiramate YD Study Group.
Neurology
46
1684
1690
84. PriviteraMFinchamRPenryJReifeRKramerL
1996
Topiramate placebo-controlled dose-ranging trial in refractory partial epilepsy using 600-, 800-, and 1,000-mg daily dosages. Topiramate YE Study Group.
Neurology
46
1678
1683
85. ShariefMViteriCBen-MenachemEWeberMReifeR
1996
Double-blind, placebo-controlled study of topiramate in patients with refractory partial epilepsy.
Epilepsy Res
25
217
224
86. Korean
1999
Topiramate in medically intractable partial epilepsies: double-blind placebo-controlled randomized parallel group trial. Korean Topiramate Study Group.
Epilepsia
40
1767
1774
87. YenDJYuHYGuoYCChenCYiuCH
2000
A double-blind, placebo-controlled study of topiramate in adult patients with refractory partial epilepsy.
Epilepsia
41
1162
1166
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