Modeling disease progression in acute stroke by simultaneously using the NIH Stroke Scale, Scandinavian Stroke Scale and the Barthel Index

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Modeling disease progression in acute stroke by simultaneously using the NIH Stroke Scale, Scandinavian Stroke Scale and the Barthel Index Kristin E. Karlsson Justin J. Wilkins, Mats O. Karlsson and E. Niclas Jonsson PAGE 2007-06-13 Division of Pharmacokinetics and Drug Therapy Department of Pharmaceutical Biosciences Uppsala University Sweden

Acute ischemic stroke 12 million people suffer acute ischemic strokes each year 1 One third die One third are left permanently disabled 1 Atlas of Heart Disease and Stroke, WHO, September 2004

Clinical trials in acute ischemic stroke More than 74 000 patients with acute ischemic stroke have been randomized into clinical trials over the past 35 years 1 Only one treatment has emerged from these investigations! (tpa treatment) 1 Krams M, Lees KR, Berry DA. The past is the future: Innovative Designs in Acute Stroke Therapy Trials. Stroke 2005;36;1341-1347.

Challenges in drug development The nature of stroke is challenging Multi-factorial disease Lack of informative biomarkers Several scales used Neurological assessment Functional assessment Blunt endpoints Disease progression The scales as such

Example of stroke data measured on the NIH stroke scale 40 Dropout pattern 30 Non-monotonic pattern NIHSS Score 20 10 0 20 40 60 80 100 Time (Days) Monotonic improvement pattern Approved clinical end-point = Day 90-Day0

What would the benefits of modeling be in establishing clinical efficacy in stroke? Longitudinal analysis would use all the available information within one subject Appropriate handling of dropouts With modeling is it possible to look across scales and utilize the available information optimally Easier to establish a drug effect Will increase the statistical power

Objectives To develop a single disease progression model for multiple stroke scales That can be fitted to multiple scales simultaneously That uses all assessments on all scales, including dropout

Data used in the development of the disease progression model Placebo arm from an efficacy trial of Chlomethiazole 772 patients NIH Stroke Scale Neurological assessment Scores between 42 0 Day 0, 7, 30, and 90 Scandinavian Stroke Scale Neurological assessment Scores between 0 48 Day 0, 7, 30, and 90 Barthel Index Functional assessment Scores between 0 100 (increments of 5) Day 7, 30, 60, and 90

Individual stroke scores measured on three different stroke scales 0 20 40 60 80 PatientID : 486 PatientID : 713 PatientID : 1056 1.0 0.8 0.6 Normalized scores: between 0-1 1 is good, 0 is bad 0.4 NORMALIZED SCORE 1.0 0.8 PatientID : 88 PatientID : 170 PatientID : 220 0.2 0.0 NIHSS SSS BI 0.6 0.4 0.2 0.0 0 20 40 60 80 DAY 0 20 40 60 80

A longitudinal model for a scale specific disease progression in acute stroke Time (days) Dropout NIHSS Score Best Possible Score

Schematic picture of the hierarchy of the scale specific model Improvement P1 1-P1 Decline Not Total Recovery P2 1-P2 Total Recovery Dropout P3 1-P3 Not Dropout A linear prediction of improved score A linear prediction of declined score

A longitudinal model for a scale specific disease progression in acute stroke Time (days) Dropout Dropout Dropout NIHSS Score Best Possible Score

The structure of the multi-scale model Scale specific components of the model: Probability of improvement Probability of not total recovery Relative score improvement + IIV Relative score decline + IIV Scale independent components of the model: IIV covariance on relative score improvement IIV covariance on relative score decline Dropout model

Structural covariates included in the multi-scale model Probability of Improvement Y j-1 Age Probability of Not Total Recovery NIHSS SSS BI Joint Y j-1 Δ(t j -t j-1 ) Probability of Dropout Yˆ SSS Δ(t j -t j-1 ) Relative Score Improvement Y j-1 Age Relative Score Decline Y j-1 Δ(t j -t j-1 )

Results NIH stroke scale

Results Scandinavian stroke scale

Results Barthel Index

Summary A model that recognizes similarities and accounts for differences for measurements on multiple stroke scales has been developed. It incorporates: Disease progression Structural covariates A common dropout model Covariance between interindividual variabilities across the three scales

Acknowledgements AstraZeneca, Södertälje, Sweden for providing data and financial support.