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Along with the clinical trial simulations feature, the Mediana R package can be used to obtain adjusted p-values and one-sided simultaneous confidence limits.
AdjustPvalues
functionThe AdjustPvalues
function can be used to get adjusted p-values for commonly used multiple testing procedures based on univariate p-values (Bonferroni, Holm, Hommel, Hochberg, fixed-sequence and Fallback procedures), commonly used parametric multiple testing procedures (single-step and step-down Dunnett procedures) and multistage gatepeeking procedure.
The AdjustPvalues
function requires the input of two pre-specified objects defined in the following two arguments:
pval
defines the raw p-values.
proc
defines the multiple testing procedure. Several procedures are already implemented in the Mediana package (listed below, along with the required or optional parameters to specify in the par argument):
BonferroniAdj
: Bonferroni procedure. Optional parameter: weight
.HolmAdj
: Holm procedure. Optional parameter: weight
.HochbergAdj
: Hochberg procedure. Optional parameter: weight
.HommelAdj
: Hommel procedure. Optional parameter: weight
.FixedSeqAdj
: Fixed-sequence procedure.FallbackAdj
: Fallback procedure. Required parameters: weight
.DunnettAdj
: Single-step Dunnett procedure. Required parameters: n
.StepDownDunnettAdj
: Step-down Dunnett procedure. Required parameters: n
.ChainAdj
: Family of chain procedures. Required parameters: weight
and transition
.NormalParamAdj
: Parametric multiple testing procedure derived from a multivariate normal distribution. Required parameter: corr
. Optional parameter: weight
.ParallelGatekeepingAdj
: Family of parallel gatekeeping procedures. Required parameters: family
, proc
, gamma
.MultipleSequenceGatekeepingAdj
: Family of multiple-sequence gatekeeping procedures. Required parameters: family
, proc
, gamma
.MixtureGatekeepingAdj
: Family of mixture-based gatekeeping procedures. Required parameters: family
, proc
, gamma
, serial
, parallel
.par
defines the parameters associated to the multiple testing procedure.
The AdjustPvalues
function returns a vector of adjusted p-values.
The following example illustrates the use of the AdjustedPvalues
function to get adjusted p-values for traditional nonparametric, semi-parametric and parametric procedures, as well as more complex multiple testing procedures.
For the illustration of adjustedment of raw p-values with the traditional nonparametric and semiparametric procedures, we will consider the following three raw p-values:
These p-values will be adjusted with several multiple testing procedures as specified below:
# Bonferroni, Holm, Hochberg, Hommel and Fixed-sequence procedure
proc = c("BonferroniAdj", "HolmAdj", "HochbergAdj", "HommelAdj", "FixedSeqAdj", "FallbackAdj")
In order to obtain the adjusted p-values for all these procedures, the sapply
function can be used as follows. Note that as no weight
parameter is defined, the equally weighted procedures are used to adjust the p-values. Finally, for the fixed-sequence procedure (FixedSeqAdj
), the order of the testing sequence is based on the order of the p-values in the vector.
The output is as follows:
BonferroniAdj HolmAdj HochbergAdj HommelAdj FixedSeqAdj FallbackAdj
[1,] 0.036 0.027 0.023 0.023 0.012 0.0360
[2,] 0.027 0.027 0.023 0.018 0.012 0.0270
[3,] 0.069 0.027 0.023 0.023 0.023 0.0345
In order to specify unequal weights for the three raw p-values, the weight
parameter can be defined as follows. Note that this parameter has no effect on the adjustment with the fixed-sequence procedure.
# Unequally weighted (no effect on the fixed-sequence procedure)
sapply(proc, function(x) {AdjustPvalues(rawp,
proc = x,
par = parameters(weight = c(1/2, 1/4, 1/4)))})
The output is as follows:
Consider a clinical trials comparing three doses with a Placebo based on a normally distributed endpoints. Let H1, H2 and H3 be the three null hypotheses of no effect tested in the trial:
H1: No difference between Dose 1 and Placebo
H2: No difference between Dose 2 and Placebo
H3: No difference between Dose 3 and Placebo
The treatment effect estimates, corresponding to the mean dose-placebo difference are specified below, as well as the pooled standard deviation, the sample size, the standard errors and the T-statistics associated with the three dose-placebo tests
# Treatment effect estimates (mean dose-placebo differences)
est = c(2.3,2.5,1.9)
# Pooled standard deviation
sd = 9.5
# Study design is balanced with 180 patients per treatment arm
n = 180
# Standard errors
stderror = rep(sd*sqrt(2/n),3)
# T-statistics associated with the three dose-placebo tests
stat = est/stderror
Based on the T-statistics, the raw p-values can be easily obtained:
The adjusted p-values based on the single step Dunnett and step-down Dunnett procedures are obtained as follows.
# Adjusted p-values based on the Dunnett procedures
# (assuming that each test statistic follows a t distribution)
AdjustPvalues(rawp,proc = "DunnettAdj", par = parameters(n = n))
AdjustPvalues(rawp,proc = "StepDownDunnettAdj", par = parameters(n = n))
The outputs are presented below.
For illustration, we will consider a clinical trial with two families of null hypotheses. The first family contains the null hypotheses associated with the Endpoints 1 and 2, that are considered as primary endpoints, and the second family the null hypotheses associated with the Endpoints 3 and 4 (key secondary endpoints). The null hypotheses of the secondary family will be tested if and only if at least one null hypothesis from the first family is rejected. Let H1, H2, H3 and H4 be the four null hypotheses of no effect on Endpoint 1, 2, 3 and 4 respectively tested in the trial:
H1: No difference between Drug and Placebo on Endpoint 1 (Family 1)
H2: No difference between Drug and Placebo on Endpoint 2 (Family 1)
H3: No difference between Drug and Placebo on Endpoint 3 (Family 2)
H4: No difference between Drug and Placebo on Endpoint 4 (Family 2)
The raw p-values are specified below:
# One-sided raw p-values (associated respectively with H1, H2, H3 and H4)
rawp<-c(0.0082, 0.0174, 0.0042, 0.0180)
The parameters of the parallel gatekeeping procedure are specified using the three arguments family
which specifies the hypotheses included in each family, proc
which specifies the component procedure associated with each family and gamma
which specifies the truncation parameter of each family.
# Define hypothesis included in each family (index of the raw p-value vector)
family = families(family1 = c(1, 2),
family2 = c(3, 4))
# Define component procedure of each family
component.procedure = families(family1 ="HolmAdj",
family2 = "HolmAdj")
# Truncation parameter of each family
gamma = families(family1 = 0.5,
family2 = 1)
The adjusted p-values are obtained using the AdjustedPvalues
function as specified below:
AdjustCIs
functionThe AdjustCIs
function can be used to get simultaneous confidence intervals for selected multiple testing procedures based on univariate p-values (Bonferroni, Holm and fixed-sequence procedures) and commonly used parametric multiple testing procedures (single-step and step-down Dunnett procedures).
The AdjustPvalues
function requires the input of two pre-specified objects defined in the following two arguments:
est
defines the point estimates.
proc
defines the multiple testing procedure. Several procedures are already implemented in the Mediana package (listed below, along with the required or optional parameters to specify in the par argument):
BonferroniAdj
: Bonferroni procedure. Required parameters: n
, sd
and covprob
. Optional parameter: weight
.HolmAdj
: Holm procedure. Required parameters: n
, sd
and covprob
. Optional parameter: weight
.FixedSeqAdj
: Fixed-sequence procedure. Required parameters: n
, sd
and covprob
.DunnettAdj
: Single-step Dunnett procedure. Required parameters: n
, sd
and covprob
.StepDownDunnettAdj
: Step-down Dunnett procedure. Required parameters: n
, sd
and covprob
.par
defines the parameters associated to the multiple testing procedure.
The AdjustCIs
function returns a vector lower simultaneous confidence limits.
Consider a clinical trials comparing three doses with a Placebo based on a normally distributed endpoints. Let H1, H2 and H3 be the three null hypotheses of no effect tested in the trial:
H1: No difference between Dose 1 and Placebo
H2: No difference between Dose 2 and Placebo
H3: No difference between Dose 3 and Placebo
The treatment effect estimates, corresponding to the mean dose-placebo difference are specified below, as well as the pooled standard deviation, the sample size.
# Null hypotheses of no treatment effect are equally weighted
weight<-c(1/3,1/3,1/3)
# Treatment effect estimates (mean dose-placebo differences)
est = c(2.3,2.5,1.9)
# Pooled standard deviation
sd = 9.5
# Study design is balanced with 180 patients per treatment arm
n = 180
The one-sided simultaneous confidence limits for several multiple testing procedures are obtained using the AdjustCIs
function wrapped in a sapply
function.
# Bonferroni, Holm, Hochberg, Hommel and Fixed-sequence procedure
proc = c("BonferroniAdj", "HolmAdj", "FixedSeqAdj", "DunnettAdj", "StepDownDunnettAdj")
# Equally weighted
sapply(proc, function(x) {AdjustCIs(est,
proc = x,
par = parameters(sd = sd,
n = n,
covprob = 0.975,
weight = weight))})
The output obtained is presented below:
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