Handling drop-out in longitudinal clinical trials: a comparison of the LOCF and MMRM approaches

被引:212
作者
Lane, Peter [1 ]
机构
[1] GlaxoSmithKline, Stat Res Unit, Harlow CM19 5AW, Essex, England
关键词
missing data; LOCF; MMRM; longitudinal trial; drop-out;
D O I
10.1002/pst.267
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study compares two methods for handling missing data in longitudinal trials: one using the last-observation-carried-forward (LOCF) method and one based on a multivariate or mixed model for repeated measurements (MMRM). Using data sets simulated to match six actual trials, I imposed several drop-out mechanisms, and compared the methods in terms of bias in the treatment difference and power of the treatment comparison. With equal drop-out in Active and Placebo arms, LOCF generally underestimated the treatment effect; but with unequal drop-out, bias could be much larger and in either direction. In contrast, bias with the MMRM method was much smaller; and whereas MMRM rarely caused a difference in power of greater than 20%, LOCF caused a difference in power of greater than 20% in nearly half the simulations. Use of the LOCF method is therefore likely to misrepresent the results of a trial seriously, and so is not a good choice for primary analysis. In contrast, the MMRM method is unlikely to result in serious misinterpretation, unless the drop-out mechanism is missing not at random (MNAR) and there is substantially unequal drop-out. Moreover, MMRM is clearly more reliable and better grounded statistically. Neither method is capable of dealing on its own with trials involving MNAR drop-out mechanisms,for which sensitivity analysis is needed using more complex methods. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:93 / 106
页数:14
相关论文
共 17 条
[1]  
[Anonymous], 1998, STAT PRINC CLIN TRIA
[2]  
[Anonymous], POINTS CONS MISS DAT
[3]   Marginal analysis of incomplete longitudinal binary data: A cautionary note on LOCF imputation [J].
Cook, RJ ;
Zeng, LL ;
Yi, GY .
BIOMETRICS, 2004, 60 (03) :820-828
[4]   Move over ANOVA - Progress in analyzing repeated-measures data and its reflection in papers published in the archives of general psychiatry [J].
Gueorguieva, R ;
Krystal, JH .
ARCHIVES OF GENERAL PSYCHIATRY, 2004, 61 (03) :310-317
[5]   A MULTIPLE IMPUTATION STRATEGY FOR CLINICAL-TRIALS WITH TRUNCATION OF PATIENT DATA [J].
LAVORI, PW ;
DAWSON, R ;
SHERA, D .
STATISTICS IN MEDICINE, 1995, 14 (17) :1913-1925
[6]  
Little R., 1987, STAT ANAL MISSING DA
[7]  
Mallinckrodt C H, 2001, J Biopharm Stat, V11, P9, DOI 10.1081/BIP-100104194
[8]   Choice of the primary analysis in longitudinal clinical trials [J].
Mallinckrodt, CH ;
Watkin, JG ;
Molenberghs, G ;
Carroll, RJ .
PHARMACEUTICAL STATISTICS, 2004, 3 (03) :161-169
[9]   Type I error rates from likelihood-based repeated measures analyses of incomplete longitudinal data [J].
Mallinckrodt, CH ;
Kaiser, CJ ;
Watkin, JG ;
Detke, MJ ;
Molenberghs, G ;
Carroll, RJ .
PHARMACEUTICAL STATISTICS, 2004, 3 (03) :171-186
[10]   Type I error rates from mixed effects model repeated measures versus fixed effects anova with missing values imputed via last observation carried forward [J].
Mallinckrodt, CH ;
Clark, WS ;
David, SR .
DRUG INFORMATION JOURNAL, 2001, 35 (04) :1215-1225