Introduction to
personalized
The personalized package aims to provide an entire
analysis pipeline that encompasses a broad class of statistical methods
for subgroup identification / personalized medicine.
The general analysis pipeline is as follows:
- Construct propensity score function and check propensity score
diagnostics
- Choose and fit a subgroup identification model
- Estimate the resulting treatment effects among estimated
subgroups
- Visualize and examine model and subgroup treatment effects
The available subgroup identification models are those under the
purview of the general subgroup identification framework proposed by
Chen, et al. (2017). In this section we will give a brief summary of
this framework and what elements of it are available in the
personalized package.
In general we are interested in understanding the impact of a
treatment on an outcome and in particular determining if and how
different patients respond differently to a treatment in terms of their
expected outcome. Assume the outcome we observe \(Y\) is such that larger values are
preferable. In addition to the outcome, we also observe patient
covariate information \(X \in
\mathbb{R}^p\) and the treatment status \(T \in \{-1,1\}\), where \(T = 1\) indicates that a patient received
the treatment, and \(T = -1\) indicates
a patient received the control. For the purposes of this package, we
consider an unspecified form for the expected outcome conditional on the
covariate and treatment status information: \[E(Y|T, X) = g(X) + T\Delta(X)/2,\] where
\(\Delta(X) \equiv E(Y|T=1, X) - E(Y|T=-1,
X)\) is of primary interest and \(g(X)
\equiv \frac{1}{2}\{E(Y|T=1, X) + E(Y|T=-1, X) \}\) represents
covariate main effects. Here, \(\Delta(X)\) represents the interaction
between treatment and covariates and thus drives heterogeneity of main
effect. The purpose of the package is in estimation of \(\Delta(X)\) or monotone transformations of
\(\Delta(X)\) which can be used to
stratify the population into subgroups (e.g. a subgroup of patients who
benefit from the treatment and a subgroup who does not benefit).
We call the term \(\Delta(X)\) a
benefit score, as it reflects how much a patient is expected to benefit
from a treatment in terms of their outcome. For a patient with \(X = x\), if \(\Delta(x) > 0\) (assuming larger
outcomes are better), the treatment is beneficial in terms of the
expected outcome, and if \(\Delta(X) \leq
0\), the control is better than the treatment. Hence to identify
which subgroup of patients benefits from a treatment, we seek to
estimate \(\Delta(X)\).
In the framework of Chen, et al. (2017), there are two main methods
for estimating subgroups. The first is called the weighting method. The
weighting method estimates \(\Delta(X)\) (or monotone transformations of
it) by minimizing the following objective function with respect to \(f(X)\): \[L_W(f)
= \frac{1}{n}\sum_{i = 1}^n\frac{M(Y_i, T_i\times f(x_i)) }{
{T_i\pi(x_i)+(1-T_i)/2} },\] where \(\pi(x) = Pr(T = 1|X = x)\) is the
propensity score function. Here, \(\hat{f}\) is our estimated benefit score.
Hence \(\hat{f} = \mbox{argmin}_f
L_W(f)\) is our estimate of \(\Delta(X)\). If we want a simple functional
form for the estimate \(\hat{f}\), we
can restrict the form of \(f\) such
that it is a linear combination of the covariates, i.e. \(f(X) = X^T\beta\). Hence \(\hat{f}(X) = X^T\hat{\beta}\).
The A-learning estimator is the minimizer of \[L_A(f) = \frac{1}{n}\sum_{i = 1}^n M(Y_i,
{\{(T_i+1)/2 -\pi(x_i)\} } {\times f(x_i))}.\]
Choice of \(M\) function
The personalized package offers a flexible range of
choices both for the form of \(f(X)\)
and also for the loss function \(M(y,
v)\). Most choices of \(f\) and
\(M\) can be used for either the
weighting method or for the A-learning method. In this package, we limit
the use of \(M\) to natural choices
corresponding to the type of outcome. The squared error loss \(M(y, v) = (v - y) ^ 2\) corresponds to
continuous responses but can also be used for binary outcomes, however
the logistic loss \(M(y, v) = y \cdot log(1 +
\exp\{-v\})\) corresponds to binary outcomes and the loss
associated with the negative partial likelihood of the Cox proportional
hazards model corresponds to time-to-event outcomes.
| Squared Error |
C/B/CT |
\(M(y, v) = (v - y) ^
2\) |
| OWL Logistic |
C/B/CT |
\(M(y, v) = y\log(1 +
\exp\{-v\})\) |
| OWL Logistic Flip |
C/B/CT |
\(M(y, v) = \vert y\vert
\log(1 + \exp\{-\mbox{sign}(y)v\})\) |
| OWL Hinge |
C/B/CT |
\(M(y, v) = y\max(0, 1 -
v)\) |
| OWL Hinge Flip |
C/B/CT |
\(M(y, v) = \vert
y\vert\max(0, 1 - \mbox{sign}(y)v)\) |
| Logistic |
B |
\(M(y, v) = -[yv - \log(1 +
\mbox{exp}\{-v\})]\) |
| Poisson |
CT |
\(M(y, v) = -[yv -
\exp(v)]\) |
| Cox |
TTE |
\(M(y, v) = -\left\{
\int_0^\tau\left( v - \log[E\{ e^vI(X \geq u) \}] \right)\mathrm{d} N(u)
\right\}\) |
where “C” indicates usage for continuous outcomes, “B” indicates
usage for binary outcomes, “CT” indicates usages for count outcomes, and
“TTE” indicates usages for time-to-event outcomes, and for the last loss
\(y = (X, \delta) = \{ \widetilde{X} \wedge C,
I(\widetilde{X} \leq t) \}\), \(\widetilde{X}\) is the survival time, &
\(C\) is the censoring time, \(N(t) = I(\widetilde{X} \leq t)\delta\), and
\(\tau\) & is fixed time point
where \(P(X \geq \tau) > 0\).
Choice of \(f\)
The choices of \(f\) offered in the
personalized package are varied. A familiar, interpretable
choice of \(f(X)\) is \(X^T\beta\). Also offered is an additive
model, i.e. \(f(X) = \sum_{j =
1}^pf_j(X_j)\); this option is accessed through use of the
mgcv package, which provides estimation procedures for
generalized additive models (GAMs). Another flexible, but less
interpretable choice offered here is related to gradient boosted
decision trees, which model \(f\) as
\(f(X) = \sum_{k = 1}^Kf_k(X)\), where
each \(f_k\) is a decision tree
model.
Variable
Selection
For subgroup identification models with \(f(X) = X^T\beta\), the
personalized package also allows for variable selection.
Instead of minimizing \(L_W(f)\) or
\(L_A(f)\), we instead minimize a
penalized version: \(L_W(f) +
\lambda||\beta||_1\) or \(L_A(f) +
\lambda||\beta||_1\).
Extension to
multi-category treatments
Often, multiple treatment options are available for patients instead
of one treatment option and a control and the researcher may wish to
understand which of all treatment options are the best for which
patients. Extending the above methodology to multi-category treatment
results in added complications, and in particular there is no
straightforward extension of the A-learning method for multiple
treatment settings. In the supplementary material of , the weighting
method was extended to estimate a benefit score corresponding to each
level of a treatment subject to a sum-to-zero constraint for
identifiability.
In particular,
we are interested in estimating (the sign) of \[\begin{eqnarray}
\Delta_{kl}(x) \equiv
\{ E(Y | T = k, { X} = { x}) - E(Y | T = l, X = { x}) \}
\label{definition of Delta_kl}
\end{eqnarray}\] If \(\Delta_{kl}(x)
> 0\), then treatment \(k\)
is preferable to treatment \(l\) for a
patient with \(X = x\). For each
patient, evaluation of all pairwise comparisons of the \(\Delta_{kl}(x)\) indicates which treatment
leads to the largest expected outcome. The weighting estimators of the
benefit scores are the minimizers of the following loss function: \[\begin{equation} \label{eqn:weighting_mult}
L_W(f_1, \dots, f_{K}) = \frac{1}{n}\sum_{i = 1}^n\frac{\boldsymbol
M(Y_i, \sum_{k = 1}^{K}I(T_{i} = k)\times f_k(x_i) ) }{ { Pr(T = T_i |
X = x_i)} },
\end{equation}\] subject to \(\sum_{k =
1}^{K}f_k(x_i) = 0\). Clearly when \(K
= 2\), this loss function is equivalent to (\(\ref{eqn:weighting}\)).
Estimation of the benefit scores in this model is still challenging
without added modeling assumptions, as enforcing \(\sum_{k = 1}^{K}f_k(x_i) = 0\) may not
always be feasible using existing estimation routines. However, if each
\(\Delta_{kl}(X)\) has a linear form,
i.e. \(\Delta_{kl}(X) = X^\top\boldsymbol
\beta_k\) where \(l\) represents
a reference treatment group, estimation can then easily be fit into the
same computational framework as for the simpler two treatment case by
constructing an appropriate design matrix. Thus, for multiple treatments
the package is restricted to linear estimators of the benefit scores.
For instructive purposes, consider a scenario with three treatment
options, \(A\), \(B\), and \(C\). Let \(\boldsymbol X = ({\boldsymbol X}_A^\top,
{\boldsymbol X}_B^\top, {\boldsymbol X}_C^\top )^\top\) be the
design matrix for all patients, where each \({\boldsymbol X}_k^\top\) is the sub-design
matrix of patients who received treatment \(k\). Under \(\Delta_{kl}(X) = X^\top\boldsymbol
\beta_k\) with \(l\) as the
reference treatment, we can construct a new design matrix which can then
be provided to existing estimation routines in order to minimize (\(\ref{eqn:weighting_mult}\)). With treatment
\(C\) as the reference treatment, the
design matrix is constructed as \[
\widetilde{{\boldsymbol X}} = \mbox{diag}(\boldsymbol J)\begin{pmatrix}
{\boldsymbol X}_A & \boldsymbol 0 \\
\boldsymbol 0 & {\boldsymbol X}_B \\
{\boldsymbol X}_C & {\boldsymbol X}_C
\end{pmatrix},
\] where the \(i\)th element of
\(\boldsymbol J\) is \(2I(T_i \neq C) - 1\) and the weight vector
\(\boldsymbol W\) is constructed with
the \(i\)th element set to \(1 / Pr(T = T_i | X = {x}_i)\). Furthermore
denote \(\widetilde{\boldsymbol \beta} =
(\boldsymbol \beta_A^\top, \boldsymbol \beta_B^\top)^\top\).
Hence \(\widetilde{{\boldsymbol
X}}^\top\widetilde{\boldsymbol \beta} = {\boldsymbol
X}_A^\top\boldsymbol \beta_A + {\boldsymbol X}_B^\top\boldsymbol \beta_B
- {\boldsymbol X}_C^\top(\boldsymbol \beta_A + \boldsymbol
\beta_B)\), and thus the sum-to-zero constraints on the benefit
scores hold by construction.
Quick Usage
Reference
First simulate some data where we know the truth. In this simulation,
the treatment assignment depends on covariates and hence we must model
the propensity score \(\pi(x) = Pr(T = 1 | X =
x)\). In this simulation we will assume that larger values of the
outcome are better.
library(personalized)
set.seed(123)
n.obs <- 1000
n.vars <- 25
x <- matrix(rnorm(n.obs * n.vars, sd = 3), n.obs, n.vars)
# simulate non-randomized treatment
xbetat <- 0.5 + 0.25 * x[,11] - 0.25 * x[,2]
trt.prob <- exp(xbetat) / (1 + exp(xbetat))
trt <- rbinom(n.obs, 1, prob = trt.prob)
# simulate delta
delta <- (0.5 + x[,2] - 0.5 * x[,3] - 1 * x[,11] + 1 * x[,1] * x[,12] )
# simulate main effects g(X)
xbeta <- x[,1] + x[,11] - 2 * x[,12]^2 + x[,13] + 0.5 * x[,15] ^ 2
xbeta <- xbeta + delta * (2 * trt - 1)
# simulate continuous outcomes
y <- drop(xbeta) + rnorm(n.obs)
Creating and Checking
Propensity Score Model
The first step in our analysis is to construct a model for the
propensity score. In the personalized package, we need to
wrap this model in a function which inputs covariate values and the
treatment statuses and outputs a propensity score between 0 and 1. Since
there are many covariates, we use the lasso to select variables in our
propensity score model:
# create function for fitting propensity score model
prop.func <- function(x, trt)
{
# fit propensity score model
propens.model <- cv.glmnet(y = trt,
x = x,
family = "binomial")
pi.x <- predict(propens.model, s = "lambda.min",
newx = x, type = "response")[,1]
pi.x
}
We then need to make sure the propensity scores have sufficient
overlap between treatment groups. We can do this with the
check.overlap() function, which plots densities or
histograms of the propensity scores for each of the treatment
groups:
check.overlap(x, trt, prop.func)
We can see that the propensity scores mostly have common support
except a small region near 0 where there are no propensity scores for
the treatment arm.
Fitting Subgroup
Identification Models
The next step is to choose and fit a subgroup identification model.
In this example, the outcome is continuous, so we choose the squared
error loss function. We also choose the model type (either the weighting
or the A-learning method). The main function for fitting subgroup
identification models is fit.subgroup. Since there are many
covariates, we choose a loss function with a lasso penalty to select
variables. The underlying fitting function here is
cv.glmnet(). We can pass to fit.subgroup()
arguments of the cv.glmnet() function, such as
nfolds for the number of cross validation folds.
subgrp.model <- fit.subgroup(x = x, y = y,
trt = trt,
propensity.func = prop.func,
loss = "sq_loss_lasso",
nfolds = 5) # option for cv.glmnet
summary(subgrp.model)
## family: gaussian
## loss: sq_loss_lasso
## method: weighting
## cutpoint: 0
## propensity
## function: propensity.func
##
## benefit score: f(x),
## Trt recom = 1*I(f(x)>c)+0*I(f(x)<=c) where c is 'cutpoint'
##
## Average Outcomes:
## Recommended 0 Recommended 1
## Received 0 -7.792 (n = 177) -19.5361 (n = 224)
## Received 1 -15.8839 (n = 437) -10.8195 (n = 162)
##
## Treatment effects conditional on subgroups:
## Est of E[Y|T=0,Recom=0]-E[Y|T=/=0,Recom=0]
## 8.0919 (n = 614)
## Est of E[Y|T=1,Recom=1]-E[Y|T=/=1,Recom=1]
## 8.7166 (n = 386)
##
## NOTE: The above average outcomes are biased estimates of
## the expected outcomes conditional on subgroups.
## Use 'validate.subgroup()' to obtain unbiased estimates.
##
## ---------------------------------------------------
##
## Benefit score quantiles (f(X) for 1 vs 0):
## 0% 25% 50% 75% 100%
## -9.1348 -2.5640 -0.7204 0.8641 7.8583
##
## ---------------------------------------------------
##
## Summary of individual treatment effects:
## E[Y|T=1, X] - E[Y|T=0, X]
##
## Min. 1st Qu. Median Mean 3rd Qu. Max.
## -18.270 -5.128 -1.441 -1.526 1.728 15.717
##
## ---------------------------------------------------
##
## 3 out of 25 interactions selected in total by the lasso (cross validation criterion).
##
## The first estimate is the treatment main effect, which is always selected.
## Any other variables selected represent treatment-covariate interactions.
##
## Trt1 V2 V11 V21
## Estimate -0.8104 0.7112 -0.353 0.2706
We can then plot the outcomes of patients in the different
subgroups:
Alternatively, we can create an interaction plot. This plot
represents the average outcome within each subgroup broken down by
treatment status. If the lines in the interaction plots cross, that
indicates there is a subgroup treatment effect.
plot(subgrp.model, type = "interaction")
Evaluating Treatment
Effects within Estimated Subgroups
Unfortunately, if we simply look at the average outcome within each
subgroup, this will give us a biased estimate of the treatment effects
within each subgroup as we have already used the data to estimate the
subgroups. Instead, to get a valid estimate of the subgroup treatment
effects we can use a bootstrap approach to correcting for this bias. We
can alternatively repeatedly partition our data into training and
testing samples. In this procedure for each replication we fit a
subgroup model using the training data and then evaluate the subgroup
treatment effects on the testing data. The argument B
specifies the number of replications and the argument
train.fraction specifies what proportion of samples are for
training in the training and testing partitioning method. Normally this
would be set to a very large number, such as 500 or 1000.
Both of these approaches can be carried out using the
validate.subgroup() function.
validation <- validate.subgroup(subgrp.model,
B = 10L, # specify the number of replications
method = "training_test_replication",
train.fraction = 0.75)
validation
## family: gaussian
## loss: sq_loss_lasso
## method: weighting
##
## validation method: training_test_replication
## cutpoint: 0
## replications: 10
##
## benefit score: f(x),
## Trt recom = 1*I(f(x)>c)+0*I(f(x)<=c) where c is 'cutpoint'
##
## Average Test Set Outcomes:
## Recommended 0 Recommended 1
## Received 0 -10.0324 (SE = 3.0877, n = 46.2) -15.6445 (SE = 3.9982, n = 56)
## Received 1 -15.3881 (SE = 2.3438, n = 105.8) -12.0415 (SE = 3.4534, n = 42)
##
## Treatment effects conditional on subgroups:
## Est of E[Y|T=0,Recom=0]-E[Y|T=/=0,Recom=0]
## 5.3557 (SE = 4.7726, n = 152)
## Est of E[Y|T=1,Recom=1]-E[Y|T=/=1,Recom=1]
## 3.603 (SE = 4.4692, n = 98)
##
## Est of
## E[Y|Trt received = Trt recom] - E[Y|Trt received =/= Trt recom]:
## 4.1217 (SE = 3.2018)
We can then plot the average outcomes averaged over all replications
of the training and testing partition procedure:
From the above plot we can evaluate what the impact of the subgroups is.
Among patients for whom the model recommends the control is more
effective than the treatment, we can see that those who instead take the
treatment are worse off than patients who take the control. Similarly,
among patients who are recommended the treatment, patients who take the
treatment are better off on average than patients who do not take the
treatment.
Similarly, we can create an interaction plot of either the bootstrap
bias-corrected means within the different subgroups or the average test
set means within subgroups. Here, lines crossing is an indicator of
differential treatment effect between the subgroups.
plot(validation, type = "interaction")
We can also compare the validation results with the results on the
observed data:
plotCompare(subgrp.model, validation, type = "interaction")
Note that the estimated treatment effects within subgroups are
attenuated for the validated results. It is common for the estimated
treatment effects within subgroups to be overly-optimistic based on the
training data.
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
