SMHS MethodsHeterogeneity HTE

Methods for Studying Heterogeneity of Treatment Effects, Case-Studies of Comparative Effectiveness Research - Methods and Approaches for HTE Analytics

Overview

Recursive partitioning is a data mining technique for exploring structure and patterns in complex data. It facilitates the visualization of decision rules for predicting categorical (classification tree) or continuous (regression tree) outcome variables. The R rpart package¹ provides the tools for Classification and Regression Tree (CART) modeling, conditional inference trees, and random forests. Additional resources include an Introduction to Recursive Partitioning Using the RPART Routines². The Appendix includes description of the main CART analysis steps.

install.packages("rpart")
library("rpart")

CART

Classification and Regression Tree (CART) is a decision-tree based technique that considers how variation observed in a given response variable (continuous or categorical) can be understood through a systematic deconstruction of the overall study population into subgroups, using explanatory variables of interest. For HTE analysis, CART is best suited for early-stage, exploratory analyses. Its relative simplicity can be powerful in identifying basic relationships between variables of interest, and thus identify potential subgroups for more advanced analyses. The key to CART is its ‘systematic’ approach to the development of the subgroups, which are constructed sequentially through repeated, binary splits of the population of interest, one explanatory variable at a time. In other words, each ‘parent’ group is divided into two ‘child’ groups, with the objective of creating increasingly homogeneous subgroups. The process is repeated and the subgroups are then further split, until no additional variables are available for further subgroup development. The resulting tree structure is oftentimes overgrown, but additional techniques are used to ‘trim’ the tree to a point at which its predictive power is balanced against issues of over-fitting. Because the CART approach does not make assumptions regarding the distribution of the dependent variable, it can be used in situations where other multivariate modeling techniques often used for exploratory predictive risk modeling would not be appropriate – namely in situations where data are not normally distributed.

CART analyses are useful in situations where there is some evidence to suggest that HTE exists, but the subgroups defining the heterogeneous response are not well understood. CART allows for an exploration of response in a myriad of complex subpopulations, and more recently developed ensemble methods (such as Bayesian Additive Regression Trees) allow for more robust analyses through the combination of multiple CART analyses.

Example Fifth Dutch growth study

# Let’s use the Fifth Dutch growth study (2009) fdgs3. Is it true that “the world’s tallest nation has stopped growing taller: the height of Dutch children from 1955 to 2009”4?

#install.packages("mice")
library("mice")
?fdgs
head(fdgs)

	ID	Reg	Age	Sex	HGT	WGT	HGT.Z	WGT.Z
1	100001	West	13.09514	boy	175.5	75.0	1.751	2.410
2	100003	West	13.81793	boy	148.4	40.0	2.292	1.494
3	100004	West	13.97125	boy	159.9	46.5	0.743	0.783
4	100005	West	13.98220	girl	159.7	46.5	0.743	0.783
5	100006	West	13.52225	girl	160.3	47.8	0.414	0.355
6	100018	East	10.21492	boy	157.8	39.7	2.025	0.823

summary(fdgs)        
summary(fdgs)

ID	Reg	Age	Sex	HGT
Min.:100001	North:732	Min.:0.008214	boy:4829	Min.:46.0
1st Qu.:106353	East:2528	1st Qu.:1.618754	girl:5201	1st Qu.:83.8
Median:203855	South:2931	Median:8.084873		Median:131.5
Mean:180091	West:2578	Mean:8.157936		Mean:123.9
3rd Qu.210591	City:1261	3rd Qu.:13.547570		3rd Qu.:162.3
Max:401955		Max.:21.993155		Max.:208.0
				NA's: 23

(1) Classification Tree

Let's use the data frame fdgs to predict Region, from Age, Height, and Weight.

# grow tree 
fit.1 <- rpart(reg ~ age + hgt + wgt,   method="class", data= fdgs[,-1])

printcp(fit.1) 	# display the results 
plotcp(fit.1) 	# visualize cross-validation results 
summary(fit.1) 	# detailed summary of splits

# plot tree 
par(oma=c(0,0,2,0))
plot(fit.1, uniform=TRUE,  margin=0.3, main="Classification Tree for Region (FDGS Data)")
text(fit.1, use.n=TRUE, all=TRUE, cex=1.0)

# create a better plot of the classification tree 
post(fit.1, title = "Classification Tree for Region (FDGS Data)", file = "")

(2) Pruning the tree

pruned.fit.1<- prune(fit.1, cp=   fit.1$\$$cptable[which.min(fit.1$\$$\$$cptable[,"xerror"]),"CP"])

 # plot the pruned tree 
 plot(pruned.fit.1, uniform=TRUE,  main="Pruned Classification Tree for Region (FDGS Data)")
 text(pruned.fit.1, use.n=TRUE, all=TRUE, cex=1.0)
 post(pruned.fit.1,  title = "Pruned Classification Tree for Region (FDGS Data)")

Not much change, as the initial tree is not complex!

===='"`UNIQ--h-6--QINU`"'(3) Random Forests ====
Random forests may improve predictive accuracy by generating a large number of bootstrapped trees (based on random samples of variables). It classifies cases using each tree in this new "forest", and decides the final predicted outcome by combining the results across all of the trees (an average in regression, a majority vote in classification). See the <b>randomForest</b> package<sup>5</sup>. 

 library(randomForest)
 fit.2 <- randomForest(reg ~ age + hgt + wgt,   method="class", na.action = na.omit, data= fdgs[,-1])
 print(fit.2) 		# view results 
 importance(fit.2) 	# importance of each predictor 

Note on missing values/incomplete data: If the data have missing values, we have 3 choices:

1.	Use a different tool (rpart handles missing values well)

2.	Impute the missing values

3.	For a small number of missing cases, we can use na.action = na.omit

==='"`UNIQ--h-7--QINU`"'Latent growth and growth mixture modeling (LGM/GMM)===

LGM and GMM represent structural equation modeling techniques that capture inter-individual differences in longitudinal change corresponding to a particular treatment. For instance, patients’ different timing patterns of the treatment effects may represent the underlying sources of HTE. LGM distinguish if (yes/no) and how (fast/slow, temporary/lasting) patients respond to treatment. The heterogeneous individual growth trajectories are estimated from intra-individual changes over time by examining common population parameters, i.e., slopes, intercepts, and error variances. Suppose each individual has unique initial status (intercept) and response rate (slope) during a specific time interval. Then the variances of the individuals’ baseline measures (intercepts) and changes (slopes) in health outcomes will represent the degree of HTE. The LGM-identified HTE of individual growth curves can be attributed to observed predictors, including both fixed and time varying covariates.

LGM assumes that all individuals are from the same population (too restrictive in some cases). If the HTE is due to observed demographic variables, such as age, gender, and marital status, one may utilize multiple-group LGM. Despite its successful applications for modeling longitudinal change, there may be multiple subpopulations with unobserved heterogeneities. Growth mixture modeling (GMM) extends LGM to allow the identification and prediction of unobserved subpopulations in longitudinal data analysis. Each unobserved subpopulation may constitute its own latent class and behave differently than individuals in other latent classes. Within each latent class, there are also different trajectories across individuals; however, different latent classes don’t share common population parameters. Suppose we are interested in studying retirees’ psychological well-being change trajectory when multiple unknown subpopulations exist. We can add another layer (a latent class variable) on the LGM framework so that the unobserved latent classes can be inferred from the data. The covariates in GMM are designed to affect growth factors distinctly across different latent classes. Therefore, there are two types of HTE: 1) the latent class variable in GMM divides individuals into groups with different growth curves; and 2) coefficient estimates vary across latent classes.

<b>Latent variables</b> are not directly observed – they are inferred (via a model) from other actually observed and directly measured variables. Models that explain observed variables in terms of latent variables are called latent variable models. Then the latent (unobserved) variable is discrete, it’s referred to as <b>latent class variable.</b>

Breast Cancer Example: Recall the LMER package, earlier review discussions, where Linear Mixed Model (LMM) are used for longitudinal data to examine change over time of outcomes according relative to predictive covariates. LMM assumptions include:

<b>(i)</b> continuous longitudinal outcome

<b>(ii)</b> Gaussian random-effects and errors

<b>(iii)</b> linearity of the relationships with the outcome

<b>(iv)</b> homogeneous population

<b>(v)</b> missing at random data

The objectives of LGM/GMM models (see <b>Latent Class Mixed Models, lcmm</b> R package<sup>6</sup>,<sup>7</sup>) are to extend the linear mixed model estimation to:

<b>(i)</b>	heterogeneous populations (relax (iv) above). Use <mark><b>hlme</b> for latent class linear mixed models</mark> (i.e. Gaussian continuous outcome)

<b>(ii)</b>	other types of longitudinal outcomes : ordinal, (bounded) quantitative non-Gaussian outcomes (relax (i), (ii), (iii), (iv)). Use <b>lcmm</b> for general latent class mixed models with outcomes of different nature

<b>(iii)</b>	joint analysis of a time-to-event (relax (iv), (v)). Use <b>Jointlcmm</b> for joint latent class models with a longitudinal outcome and a right-censored (left-truncated) time-to-event</blockquote>

Let’s use these data (http://www.ats.ucla.edu/stat/data/hdp.csv), representing cancer phenotypes and predictors (e.g., "IL6", "CRP", "LengthofStay", "Experience") and outcome measures (e.g., remission) collected on patients, nested within doctors (DID) and within hospitals (HID).

We can illustrate the latent class linear mixed models implemented in <b>hlme</b> through a study of the quadratic trajectories of the response (remission) with TumorSize, adjusting for CO2*Pain interaction and assuming correlated random-effects for the functions of SmokingHx and Sex. To estimate the corresponding standard linear mixed model using 1 latent class where CO2 interacts with Pain:

 # install.packages("lcmm")
 library("lcmm")

 hdp <- read.csv("http://www.ats.ucla.edu/stat/data/hdp.csv")
 hdp <- within(hdp, {
 Married <- factor(Married, levels = 0:1, labels = c("no", "yes"))
 DID <- factor(DID)
 HID <- factor(HID)
 })

add a new subject ID column (last column in the data, “ID”), this is necessary for the hmle call
hdp$\$$ID <- seq.int(nrow(hdp))

model.hlme <- hlme(remission ~ IL6 + CRP + LengthofStay + Experience + I(tumorsize^2) + co2*pain + I(tumorsize^2)*pain, random=~ SmokingHx + Sex, subject='ID', data=hdp, ng=1)
summary(model.hlme)

Heterogenous linear mixed model 
fitted by maximum likelihood method 

hlme(fixed = remission ~ IL6 + CRP + LengthofStay + Experience + 
I(tumorsize^2) + co2 * pain + I(tumorsize^2) * pain, random = ~SmokingHx + 
Sex, subject = "ID", ng = 1, data = hdp)

Statistical Model: 
Dataset: hdp 
Number of subjects: 8525 
Number of observations: 8525 
Number of latent classes: 1 
Number of parameters: 21  

Iteration process: 	
Convergence criteria satisfied 
Number of iterations:  34 
Convergence criteria: parameters= 1.2e-09 
: likelihood= 8.3e-06 
: second derivatives= 2.7e-05 

Goodness-of-fit statistics: 
maximum log-likelihood: -5223.9  
AIC: 10489.79  
BIC: 10637.86

Maximum Likelihood Estimates:

Fixed effects in the Longitudinal Model:

	coef	Se	Wald	p-value
Intercept	0.28636	0.24314	1.178	0.23890
IL6	-0.01134	0.00183	-6.184	0.00000
CRP	-0.00674	0.00167	-4.043	0.00005
LengthofStay	-0.04834	0.00463	-10.436	0.00000
Experience	0.01695	0.00119	14.263	0.00000
I(tumorsize^2)	0.00000	0.00001	-0.076	0.93953
co2	-0.03549	0.16204	-0.219	0.82663
pain	0.03930	0.04278	0.919	0.35832
co2:pain	-0.01489	0.02871	-0.519	0.60395
I(tumorsize^2):pain	0.00000	0.00000	0.553	0.58045

Variance-covariance matrix of the random-effects

	intercept	SmokingHxformer	SmokingHxnever	Sexmale
intercept	0.19310943
SmokingHxformer	-0.10617988	0.209155186
SmokingHxnever	-0.12388534	0.068342049	2.262655e-01
Sexmale	-0.08130975	-0.007353491	-1.873934e-05	0.1730187

Residual standard error:

coef: 0.1299767

se: 1.187426

Results interpretation:

(1) The first part of the summary provides information about the dataset, the number of subjects, observations, observations deleted (since by default, missing observations are deleted), number of latent classes and number of parameters.

(2) Next, details about the algorithm convergence is provided along with the number of iterations, the convergence criteria, and the information indicating if the model converged correctly: "convergence criteria satisfied".

(3) The maximum log-likelihood, Akaike criterion (AIC) and Bayesian Information criterion (BIC) are reported.

(4) Estimates of parameters, the estimated standard error, the Wald Test statistics (with Normal approximation) and the corresponding p-values are reported below.

(5) For the random-effect distribution, the estimated matrix of covariance of the random-effects is displayed.

(6) The standard error of the residuals is given along with its estimated standard error.

(7) The effect of TumorSize seems not associated with change over Pain of Remission. This may be formally assessed using a multivariate Wald test:

WaldMult(model.hlme, pos=c(6,8)) 
# pos - a vector containing the indices in model.hlme of the parameters to test
Wald Test p_value
I(tumorsize^2) = pain = 0   0.85562 0.65193

We may consider the model with an adjustment for CRP only on the intercept. Below we estimate the corresponding models for a varying number of latent classes (from 1 to 3) using the default initial values:

# Initial Model: model.hlme <- hlme(remission ~ IL6 + CRP + LengthofStay + Experience + I(tumorsize^2) + co2*pain + I(tumorsize^2)*pain, random=~ SmokingHx + Sex, subject='ID', data=hdp, ng=1)

model.hlme.1 <- hlme(tumorsize ~ IL6 + CRP + LengthofStay, subject='ID', data=hdp, ng=1)
model.hlme.2 <- hlme(tumorsize ~ IL6 + CRP + LengthofStay + SmokingHx, mixture=~ SmokingHx, subject='ID', data=hdp, ng=2)
model.hlme.3 <- hlme(tumorsize ~ IL6 + CRP + LengthofStay + SmokingHx, mixture=~ SmokingHx, subject='ID', data=hdp, ng=3)

The estimation process for a varying number of latent classes can be summarized with summarytable, which gives the log-likelihood, the number of parameters, the Bayesian Information Criterion, and the posterior proportion of each class:

summarytable(model.hlme.1, model.hlme.2, model.hlme.3)
            G    loglik npm      BIC    %class1    %class2  %class3
model.hlme.1 1 -33301.82   5 66648.89 100.000000                    
model.hlme.2 2 -31592.79  11 63285.15  99.214076  0.7859238         
model.hlme.3 3 -31589.55  15 63314.86   6.357771 82.2991202 11.34311

The program took 404.65 seconds

In this example, the optimal number of latent classes according to the BIC is two (the smallest BIC). The posterior classification is described with:

postprob(model.hlme.2)

Posterior classification: 
  class1 class2
N 8458.00  67.00
%   99.21   0.79

Posterior classification table: 
    --> mean of posterior probabilities in each class 
       prob1  prob2
class1 0.8555 0.1445
class2 0.4362 0.5638

Posterior probabilities above a threshold (%): 
        class1 class2
prob>0.7  92.48   2.99
prob>0.8  77.38   0.00
prob>0.9  38.53   0.00

In this example, the first class includes a posteriori 8458 subjects (99%) while class 2 includes 67 (0.79%) subjects. Subjects were classified in class 1 with a mean posterior probability of 0.8555 %.

In class 1, 92.48% were classified with a posterior probability above 0.7 while 2.99% of the subjects were classified in class 2 with a posterior probability above 0.7. Goodness-of-fit of the model can be assessed by displaying the residuals as in figure and the mean predictions of the model as in figure, according to the time variable given in var.time:

plot(model.hlme.2)
# Figure (left panel)
plot(model.hlme.2, which="fit", var.time="Age", bty="l", ylab=" Remission ", xlab="Age", lwd=2) 
# Figure (right panel)
plot(model.hlme.2, which="fit", var.time="Age", bty="l", ylab=" Remission ", xlab="Age", lwd=2, marg=FALSE)

The latent process mixed models implemented in lcmm are illustrated through the study of the linear trajectory of ntumors with Age adjusted for Sex and assuming correlated random-effects for the intercept and Age. Lines estimate the corresponding latent process mixed model with different link functions:

model.hlme.lin <- lcmm(ntumors ~ Age*Sex, random=~ Age ,subject='ID', data=hdp)
model.hlme.beta <- lcmm(ntumors ~ Age*Sex, random=~ Age, subject='ID', data=hdp, link='beta')
model.hlme.spl <- lcmm(ntumors ~ Age*Sex, random=~ Age, subject='ID', data=hdp, link='splines')
model.hlme.spl5q <- lcmm(ntumors ~ Age*Sex, random=~ Age, subject='ID', data=hdp, link='5-quant-splines')

link function: An optional family of link functions. By default,

• "linear" option specifies a linear link function leading to a standard linear mixed model (homogeneous or heterogeneous as estimated in hlme).
• "beta" for estimating a link function from the family of Beta cumulative distribution functions, "thresholds" for using a threshold model to describe the correspondence between each level of an ordinal outcome and the underlying latent process, and
• "Splines" for approximating the link function by I-splines. For this latter case, the number of nodes and the nodes location should be also specified. The number of nodes is first entered followed by,
• -, then the location is specified with "equi", "quant" or "manual" for respectively equidistant nodes, nodes at quantiles of the marker distribution or interior nodes entered manually in argument
• intnodes. It is followed by - and finally "splines" is indicated. For example, "7-equi-splines" means I-splines with 7 equidistant nodes, "6-quant-splines" means I-splines with 6 nodes located at the quantiles of the marker distribution and "9-manual-splines" means I-splines with 9 nodes, the vector of 7 interior nodes being entered in the argument intnodes.

summary (model.hlme.lin)

General latent class mixed model fitted by maximum likelihood method 

lcmm(fixed = ntumors ~ Age * Sex, random = ~Age, subject = "ID",data = hdp)

Statistical Model: 
    Dataset: hdp 
    Number of subjects: 8525 
    Number of observations: 8525 
    Number of latent classes: 1 
    Number of parameters: 8  
    Link function: linear  

Iteration process:

    Maximum number of iteration reached without convergence 
    Number of iterations:  100 
    Convergence criteria: parameters= 5.4e-10 
                        : likelihood= 5.5e-10 
                        : second derivatives= 1 

Goodness-of-fit statistics: 
    maximum log-likelihood: -19915.24  
    AIC: 39846.49  
    BIC: 39902.89  

    Discrete posterior log-likelihood: 0  
    Discrete AIC: 16  

    Mean discrete AIC per subject: 9e-04  
    Mean UACV per subject: 0  
    Mean discrete LL per subject: 0  

Maximum Likelihood Estimates: 

Fixed effects in the longitudinal model:

                             coef Se Wald p-value
intercept (not estimated)  0.00000                
Age                        0.09491                
Sexmale                   -0.66303                
Age:Sexmale                0.01132                

Variance-covariance matrix of the random-effects:
          intercept         Age
intercept 20.5013715            
Age       -0.2889814 0.007696382

Residual standard error (not estimated) = 1

Parameters of the link function:

                        coef Se Wald p-value
Linear 1 (intercept) -0.36768                
Linear 2 (std err)    0.71432           

Objects mlin, mbeta, mspl and mspl3eq are latent process mixed models that assume the exact same trajectory for the underlying latent process but respectively a linear, BetaCDF, I-splines with 5 equidistant knots (default with link=’splines’) and I-splines with 5 knots at percentiles. mlin reduces to a standard linear mixed model (link=’linear’ by default). The only difference with a hlme object is the parameterization for the intercept and the residual standard error that are considered as rescaling parameters.

col <- rainbow(4)
plot(model.hlme.lin, which="linkfunction", bty='l', ylab="Number-of-Tumors", col=col[1], lwd=2, xlab="underlying latent process")
plot(model.hlme.beta, which="linkfunction", add=T, col=col[2], lwd=2)
plot(model.hlme.spl, which="linkfunction", add=T, col=col[3], lwd=2)
plot(model.hlme.spl5q, which="linkfunction", add=T, col=col[4], lwd=2)
legend(x="topleft",legend=c("linear", "beta","splines (5equidistant)", "splines (5 at quantiles)"), lty=1,col=col,bty="n",lwd=2)

# to obtain confidence bands use function predictlink 
link.lin <- predictlink(model.hlme.lin, ndraws=2000)

Error in predictlink.lcmm(model.hlme.spl, ndraws = 2000): 
No confidence intervals can be produced since the program did not converge properly

model.hlme.lin$\$$conv <mark># double-check the convergence of the algorithm[1] 2</mark></span>
 <span style="color:#ff0000"># status of convergence:</span>
 <span style="color:#ff0000"># =1 if the convergence criteria were satisfied,</span> 
 <span style="color:#ff0000"># =2 if the maximum number of iterations was reached,</span> 
 <span style="color:#ff0000"># =4 or 5 if a problem occured during optimisation</span>


 model.hlme.lin <- lcmm(ntumors ~ Age*Sex, random=~ Age ,subject='ID', epsY = 0.5, convB = 1e-01, convL = 1e-01, <mark>convG = 1e-01</mark>, maxiter=200, data=hdp); model.hlme.lin$conv

 <mark># Now that we have convergence, we can obtain CI’s!!!</mark>
 link.lin <- predictlink(model.hlme.lin, ndraws=2000)

 # plot(model.hlme.lin, which="linkfunction", bty='l', ylab="Number-of-Tumors", col=col[1], lwd=2, xlab="underlying latent process")
 plot(link.lin, add=TRUE, col=col[1], lty=2, lwd=2)
 legend(x="left", legend=c("95% confidence bands", "for linear fit"), lty=c(2,NA), col=c(col[1],NA), bty="n", lwd=2)

<center>[[Image:SMHS_Methods7.png|500px]] </center>

 # <mark>Repeat using the other link functions … model.hlme.beta, model.hlme.spl, …</mark>
 model.hlme.beta <- lcmm(ntumors ~ Age*Sex, random=~ Age, subject='ID', data=hdp, link='beta', 
 <mark>convB = 1e-01</mark>, convL = 1e-01, convG = 1e-01, maxiter=200); model.hlme.beta$\$$conv
link.beta <- predictlink(model.hlme.beta, ndraws=2000)
plot(link.beta, add=TRUE, col=col[2], lty=2, lwd=2)
legend(x="left", legend=c("95% confidence bands", "for BETA fit"), lty=c(3,NA), col=c(col[2],NA), bty="n", lwd=1)

Footnotes

• ¹ http://cran.r-project.org/web/packages/rpart/index.html
• ² http://www.mayo.edu/hsr/techrpt/61.pdf
• ³ http://dx.doi.org/10.1371/journal.pone.0027608
• ⁴ http://www.nature.com/pr/journal/v73/n3/abs/pr2012189a.html
• ⁵ http://stat-www.berkeley.edu/users/breiman/RandomForests/
• ⁶ http://cran.r-project.org/web/packages/lcmm/
• ⁷ http://arxiv.org/pdf/1503.00890v1.pdf

Next see: Meta-Analysis

• Back to the Heterogeneity of Treatment Effects, Case-Studies of Comparative Effectiveness Research section

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