ordinal.mams | R Documentation |
The function determines (approximately) the boundaries of a multi-arm multi-stage study with ordinal or binary endpoints for a given boundary shape and finds the required number of subjects.
ordinal.mams(
prob = c(0.35, 0.4, 0.25),
or = 2,
or0 = 1.2,
K = 4,
J = 2,
alpha = 0.05,
power = 0.9,
r = 1:2,
r0 = 1:2,
ushape = "obf",
lshape = "fixed",
ufix = NULL,
lfix = 0,
nstart = 1,
nstop = NULL,
sample.size = TRUE,
Q = 20,
parallel = TRUE,
print = TRUE
)
prob |
Vector of expected probabilities of falling into each category under control conditions. The elements must sum up to one (default=c(0.35, 0.4, 0.25)). |
or |
Interesting treatment effect on the scale of odds ratios (default=2). |
or0 |
Uninteresting treatment effect on the scale of odds ratios (default=1.2). |
K |
Number of experimental treatments (default=4). |
J |
Number of stages (default=2). |
alpha |
One-sided familywise error rate (default=0.05). |
power |
Desired power (default=0.9). |
r |
Vector of allocation ratios (default=1:2). |
r0 |
Vector ratio on control (default=1:2). |
ushape |
Shape of upper boundary. Either a function specifying the shape or one of "pocock", "obf" (the default), "triangular" and "fixed". |
lshape |
Shape of lower boundary. Either a function specifying the shape or one of "pocock", "obf", "triangular" and "fixed" (the default). |
ufix |
Fixed upper boundary (default=NULL). Only used if shape="fixed". |
lfix |
Fixed lower boundary (default=0). Only used if shape="fixed". |
nstart |
Starting point for finding the sample size (default=1). |
nstop |
Stopping point for finding the sample size (default=NULL). |
sample.size |
Logical if sample size should be found as well (default=TRUE). |
Q |
Number of quadrature points per dimension in the outer integral (default=20). |
parallel |
if TRUE (default), allows parallelisation of the computation via a user-defined strategy specified by means of the function future::plan(). If not set differently, the default strategy is sequential, which corresponds to a computation without parallelisation. |
print |
if TRUE (default), indicate at which stage the computation is. |
This function finds the (approximate) boundaries and sample size of a multi-arm multi-stage study with ordinal or binary endpoints with K active treatments plus control in which all promising treatments are continued at interim analyses as described in Magirr et al (2012). It is a wrapper around the basic mams function to facilitate its use with ordinal and binary endpoints, following ideas of Whitehead & Jaki (2009) and Jaki & Magirr (2013). For a binary endpoint the vector prob has only two elements (success/failure, yes/no, etc.). See mams for further details on the basic methodology.
An object of the class MAMS containing the following components:
prob |
Vector of expected probabilities of falling into each category
under control conditions. The elements must sum up to one
(default= |
or |
Interesting treatment effect on the scale of odds ratios
(default= |
or0 |
Uninteresting treatment effect on the scale of odds ratios
(default= |
K |
Number of experimental treatments (default= |
J |
Number of stages (default= |
alpha |
One-sided familywise error rate (default= |
power |
Desired power (default= |
r |
Vector of allocation ratios (default= |
r0 |
Vector ratio on control (default= |
ushape |
Shape of upper boundary. Either a function specifying the
shape or one of |
lshape |
Shape of lower boundary. Either a function specifying the
shape or one of |
ufix |
Fixed upper boundary (default= |
lfix |
Fixed lower boundary (default= |
nstart |
Starting point for finding the sample size
(default= |
nstop |
Stopping point for finding the sample size
(default= |
sample.size |
Logical if sample size should be found as well
(default= |
N |
Number of quadrature points per dimension in the outer integral
(default= |
parallel |
if |
print |
if |
Philip Pallmann
Jaki T., Pallmann P. and Magirr D. (2019), The R Package MAMS for Designing Multi-Arm Multi-Stage Clinical Trials, Journal of Statistical Software, 88(4), 1-25. Link: doi:10.18637/jss.v088.i04
Magirr D., Jaki T. and Whitehead J. (2012), A generalized Dunnett test for multi-arm multi-stage clinical studies with treatment selection, Biometrika, 99(2), 494-501. Link: doi:10.1093/biomet/ass002
Magirr D., Stallard N. and Jaki T. (2014), Flexible sequential designs for multi-arm clinical trials, Statistics in Medicine, 33(19), 3269-3279. Link: doi:10.1002/sim.6183
Pocock S.J. (1977), Group sequential methods in the design and analysis of clinical trials, Biometrika, 64(2), 191-199.
O'Brien P.C., Fleming T.R. (1979), A multiple testing procedure for clinical trials, Biometrics, 35(3), 549-556.
Whitehead J. (1997), The Design and Analysis of Sequential Clinical Trials, Wiley: Chichester, UK.
## An example based on the example in Whitehead & Jaki (2009)
# 2-stage design with triangular efficacy and futility boundaries
prob <- c(0.075, 0.182, 0.319, 0.243, 0.015, 0.166)
ordinal.mams(prob=prob, or=3.06, or0=1.32, K=3, J=2, alpha=0.05,
power=0.9, r=1:2, r0=1:2, ushape="triangular",
lshape="triangular")
# same example with parallelisation via separate R sessions running in the
# background
future::plan(multisession)
ordinal.mams(prob=prob, or=3.06, or0=1.32, K=3, J=2, alpha=0.05,
power=0.9, r=1:2, r0=1:2, ushape="triangular",
lshape="triangular", parallel=TRUE)
future::plan("default")
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