View source: R/continuous_functions_1-1.R
pop_pchaz | R Documentation |
Calculates hazard, cumulative hazard, survival and distribution function based on hazards that are constant over pre-specified time-intervals
pop_pchaz( Tint, lambdaMat1, lambdaMat2, lambdaProgMat, p, timezero = FALSE, int_control = list(rel.tol = .Machine$double.eps^0.4, abs.tol = 1e-09), discrete_approximation = FALSE )
Tint |
vector of length k+1, for the boundaries of k time intervals (presumably in days) with piecewise constant hazard. The boundaries should be increasing and the first one should
be |
lambdaMat1 |
matrix of dimension m-by-k, each row contains the vector of piecewise constant hazards for one subpopulation before the changeing event happens, for the intervals speciefied via |
lambdaMat2 |
matrix of dimension m-by-k, each row contains the vector piecewise constant hazards for one subpopulation after the changeing event has happened, for the intervals speciefied via |
lambdaProgMat |
matrix of dimension m-by-k, each row contains the vector of piecewise constant hazards for one subpopulation for the changeing event, for the intervals speciefied via |
p |
vector of length m for relative sizes (proportions) of the subpopulations. They should sum up to 1. |
timezero |
logical, indicating whether after the changing event the timecount, governing which interval in |
int_control |
A list with additional paramaters to be passed to the |
discrete_approximation |
if TRUE, the function uses an approximation based on discretizing the time, instead of integrating. This speeds up the calculations |
Given m subgroups with relative sizes p_1, …, p_m and
subgroup-specific survival functions S{l}(t),
the marginal survival function is the mixture S(t)=∑_{l=1}^m p_l S_{l}(t).
Note that the respective hazard function is not a linear combination of the
subgroup-specific hazard functions.
It may be calculated by the general relation λ(t)=-\frac{dS(t)}{dt}\frac{1}{S(t)}.
In each subgroup, the hazard is modelled as a piecewise constant hazard, with
the possibility to also model disease progression.
Therefore, each row of the hazard rates is used in subpop_pchaz
.
See pchaz
and subpop_pchaz
for more details.
The output includes the function values calculated for all integer time points
between 0 and the maximum of Tint
.
Note: this function may be very slow in cases where many time points need to be calculated. If this happens, use
discrete_approximation = TRUE
.
A list with class mixpch
containing the following components:
haz
Values of the hazard function.
cumhaz
Values of the cumulative hazard function.
S
Values of the survival function.
F
Values of the distribution function.
t
Time points for which the values of the different functions are calculated.
Robin Ristl, robin.ristl@meduniwien.ac.at, Nicolas Ballarini
Robin Ristl, Nicolas Ballarini, Heiko Götte, Armin Schüler, Martin Posch, Franz König. Delayed treatment effects, treatment switching and heterogeneous patient populations: How to design and analyze RCTs in oncology. Pharmaceutical statistics. 2021; 20(1):129-145.
pchaz
, subpop_pchaz
, plot.mixpch
pop_pchaz(Tint = c(0, 40, 100), lambdaMat1 = matrix(c(0.2, 0.1, 0.4, 0.1), 2, 2), lambdaMat2 = matrix(c(0.5, 0.2, 0.6, 0.2), 2, 2), lambdaProg = matrix(c(0.5, 0.5, 0.4, 0.4), 2, 2), p = c(0.8, 0.2), timezero = FALSE, discrete_approximation = TRUE)
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