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Interim analyses of data as they accumulate in laboratory experimentation
© Ludbrook; licensee BioMed Central Ltd. 2003
Received: 23 April 2003
Accepted: 21 August 2003
Published: 21 August 2003
Techniques for interim analysis, the statistical analysis of results while they are still accumulating, are highly-developed in the setting of clinical trials. But in the setting of laboratory experiments such analyses are usually conducted secretly and with no provisions for the necessary adjustments of the Type I error-rate.
Laboratory researchers, from ignorance or by design, often analyse their results before the final number of experimental units (humans, animals, tissues or cells) has been reached. If this is done in an uncontrolled fashion, the pejorative term 'peeking' has been applied. A statistical penalty must be exacted. This is because if enough interim analyses are conducted, and if the outcome of the trial is on the borderline between 'significant' and 'not significant', ultimately one of the analyses will result in the magical P = 0.05. I suggest that Armitage's technique of matched-pairs sequential analysis should be considered. The conditions for using this technique are ideal: almost unlimited opportunity for matched pairing, and a short time between commencement of a study and its completion. Both the Type I and Type II error-rates are controlled. And the maximum number of pairs necessary to achieve an outcome, whether P = 0.05 or P > 0.05, can be estimated in advance.
Laboratory investigators, if they are to be honest, must adjust the critical value of P if they analyse their data repeatedly. I suggest they should consider employing matched-pairs sequential analysis in designing their experiments.
What does the term 'interim analysis' mean? A short definition is that it refers to the repeated analyses of data as they accumulate. This is not a bad definition, since it can be applied not only to clinical trials but also to laboratory experiments.
Why does it matter? It matters in a statistical sense that is not very different from that of making multiple comparisons within the same experiment. In either case, the risk of Type I error (false-positive inference) increases progressively as the number of tests of significance increases. I have reviewed elsewhere the problem of making multiple comparisons and ways of solving it [1, 2]. Here I review the topic of making serial comparisons on data as they accumulate. To state this problem in a very crude, but nonetheless broadly accurate, fashion it is almost inevitable that if the outcome is on the borderline of significance, the outcome P ≤ 0.05 will ultimately occur – quite falsely – if enough repeated interim analyses are made.
In the context of clinical trials, the issue of interim analysis is not a new one. It has been discussed in the statistical literature since the 1960s, and has reached the level of consciousness of clinical trialists over the last few years. For instance, the number of 'hits' in a PubMed search (National Library of Medicine, Washington DC) that I conducted for (interim AND analysis) were: 1968–70 (0), 1978–80 (10), 1988–90 (67), 1998–2000 (214). In 2001–2003 there were 252 hits. In the earlier periods, papers dealt chiefly with theoretical issues. In the later periods, most were concerned with actual clinical trials.
Several statistical techniques for dealing with interim analyses of clinical trials have been described. These include, in order of appearance, the Armitage-McPherson , Pocock [4, 5], Haybittle-Peto [6, 7] and O'Brien-Fleming  methods. All these techniques depend on the interim analyses being planned in advance. Excellent, simple descriptions of these can be found in the book by Friedman et al. . A simulation study suggests that the O'Brien-Fleming technique is the most powerful of these . Lan & DeMets introduced the notion of the adaptive, α-spending, function, that could be applied to unplanned interim analyses [11, 12]. However, this has been severely criticised by theoretical statisticians . Then there is the Bayesian approach, well-described by Jennison & Turnbull , but rarely employed.
None of the techniques for interim analysis of clinical trials is applicable, or easily adaptable, to the unplanned statistical analyses of laboratory experiments, usually undertaken covertly rather than overtly.
There are good reasons and bad reasons for performing interim analyses of laboratory experiments.
A good reason is that the investigators have made, in advance, an estimate of minimal group (sample) size. But they are not confident that it is a good estimate. This may be, for instance, because they have had to base their estimate on others' published data or because it is based on a small set of pilot experiments. It is reasonable, therefore, that they should analyze the results when their estimated minimal group size has been attained. If their null hypothesis is rejected, they can stop. If not, they can then use these results to re-estimate minimal group size and carry on.
A bad reason is that the investigators have not formally estimated minimal group size, but have merely made a guess. They carry out the first round of experiments, test the results, and find that they are not quite 'significant'. So they do a few more experiments. Still not quite there. So they do a few more experiments – and so on until they achieve P = 0.05, or give up.
What solutions are there to this problem? One is to employ relatively simple methods for adjusting the critical value of P. An altogether different approach is to use a technique called matched-pairs sequential analysis. A third approach, already hinted at, is to re-estimate minimal group size.
Simple methods for adjusting the critical value of P
The Šidák inequality  plays an important role in multiple comparison procedures [1, 2]. This means that the adjusted critical value of P is given by the formula 1 - (1 - P) k , where k is the number of interim analyses and the nominal critical value of P is usually 0.05. Alternatively, the raw P value resulting from a test of significance can be adjusted by the formula P' = 1 - (1 - P)1/k .
Matched-pairs sequential analysis
A simplified description of the technique is as follows. Matched pairs of subjects are assembled, and the members of each pair are assigned randomly to one or the other treatment to be investigated. The analysis is graphical. Horizontal, V-shaped, statistically-defined, upper and lower boundaries are constructed. The outcome of the trial for each pair is scored as a preference for treatment A or treatment B, and entered into the graph. If the zigzag line described by successive pairs crosses one or the other boundary, it can safely be concluded that A is superior to B (or vice versa) at a specified nominal level of significance (for instance, two-sided P = 0.05). In the preferred closed, or restricted, design a third boundary is placed across the open end of the V. If this is crossed first, then at a specified Type II error-rate it can be concluded that there is no significant difference between the treatments . The advantage of this approach is that both the Type I and Type II error-rates are controlled, and the maximum number of matched pairs necessary to cross one or another boundary can be predicted. The coordinates of the graphical boundaries are determined by: (a) the selected two-sided Type I error-rate (2α = 0.05, 0.01); (b) the selected Type II error-rate, β, where (1 - β) = power to reject the null hypothesis; and (c) the θ statistic. Typical values of these are 2α = 0.05 or 0.01, β = 0.05, θ = 0.90 (see Fig. 1).
The strength of the matched-pairs technique is that it ensures that an inference will be reached (A>B, B>A or A = B) with a predictable maximum number of paired subjects. However, it has serious practical limitations that have greatly restricted its use in clinical trials. These are that: (a) there must be a large reservoir of eligible patients so that matching can be done; (b) the time from entry to outcome must be short compared with the expected duration of the trial; and (c) the technique cannot be applied to tests on survival curves such as the logrank (Mantel-Haenszel) test. For these reasons, group sequential analysis has been the technique preferred for clinical trials [24–26].
If even amateur biostatisticians follow the instructions given by Armitage [19, 20], they should be able to design the graphical boundaries for a closed (restricted) matched-pairs sequential analysis. If they (or reviewers) have doubts about the outcome, they can use an exact test on a single binomial to confirm the inferences (see Fig. 1).
I have been unable to find an example of its use in laboratory experiments, with the exception of my obscurely-published trial of rose preservatives . Yet there is an almost unlimited supply of laboratory animals that can be matched for characteristics such as sex, age and weight. The outcome of the experiment is usually available within hours, days or weeks. The only reservation is that if the outcome of the experiment is measured on a continuous scale, there may be some loss of power because for the purpose of graphical analysis the outcomes are converted into a binomial preference for one treatment over another.
Adjusted P values corresponding to a raw P = 0.05 for binomial and continuous outcomes, according to the number of matched-pairs tested. After Armitage et al. 
Number of pairs
Adjusted actual Pvalue (P')
Armitage gave an easily-understood account of the matched-pairs technique in 1975 . His book is out of print, but is available in libraries. Alternatively, biomedical investigators and biostatisticians can consult the original accounts [3, 16, 19], or Whitehead's book .
A third approach
In planning a prospective clinical trial, it is mandatory that minimal group sizes are estimated before the trial starts. This is insisted on by institutional human ethics committees.
Institutional animal ethics committees, at any rate in Australia, now also insist that minimal group sizes are estimated in advance. This can be done on the basis of earlier studies in the same laboratory or, second best, studies published by others. The convention is to make the estimate on the basis that the critical value of P is 0.05 at a power of 0.80 (80%). Very useful aids to making these estimates are published tables , or interactive computer programs (for instance, nQuery Advisor, Statistical Solutions, Boston MA).
But minimal group size estimates are only as accurate as the data on which they are based. Often these data are suspect, or the dataset is too small. So when investigators have done the necessary number of experiments, analysed the results, and find that P is just a little greater than 0.05, it is not unreasonable that they should re-estimate minimal group size on the basis of these experiments. If the new estimate exceeds their original one, it is not unreasonable that they should carry out further experiments so that the revised estimate is achieved. Then, it is argued, their new and definitive analysis needs no adjustment of the P value.
There has been a twofold purpose to this review. One has been to remind clinical investigators of the rules governing the interim analysis of results as they accumulate in clinical trials. These rules are very firmly established, thanks to the work of biostatisticians and of regulatory bodies. The second, and more original, reason is to acquaint biologists who are conducting laboratory experiments with the price they should pay for analyzing their results as they accumulate, usually to decide whether they need to do more experiments to 'achieve' a magical P = 0.05. Whenever I chastise experimentalists for conducting interim analyses and suggest that they are acting unstatistically, if not unethically, they react with surprise.
I hope that this review may bring experimentalists and clinical trialists closer together in their attitudes towards the interim analysis of accumulating results. I believe that laboratory experimenters have a good deal to learn from clinical trialists. In particular, I commend to them matched-pairs sequential analysis as a technique for designing and analyzing their experiments.
The author was responsible for all aspects of this paper.
I am most grateful for the critical comments and suggestions on earlier versions of the manuscript from epidemiologists and laboratory biomedical scientists, and from the two reviewers. I do not name them for fear that it might be thought that they approved. Blackwell Publications gave permission for me to reproduce Figure 5.3 from Armitage  as Figure 2.
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