speff: Semiparametric efficient estimation and testing for a...

In speff2trial: Semiparametric Efficient Estimation for a Two-Sample Treatment Effect

Semiparametric efficient estimation and testing for a two-sample treatment effect with a quantitative or dichotomous endpoint

Description

speff conducts estimation and testing of the treatment effect in a 2-group randomized clinical trial with a quantitative or dichotomous endpoint. The method is a special case of Robins, Rotnitzky, and Zhao (1994, JASA). It improves efficiency by leveraging baseline predictors of the endpoint. The method uses inverse probability weighting to provide unbiased estimation when the endpoint is missing at random.

Usage

speff(formula, endpoint=c("quantitative", "dichotomous"), data,
      postrandom=NULL, force.in=NULL, nvmax=9, 
      method=c("exhaustive", "forward", "backward"), 
      optimal=c("cp", "bic", "rsq"), trt.id, conf.level=0.95, 
      missCtrl=NULL, missTreat=NULL, endCtrlPre=NULL, 
      endTreatPre=NULL, endCtrlPost=NULL, endTreatPost=NULL)

Arguments

formula	a formula object with the response on the left of the ~ operator, and the linear predictor on the right. The linear predictor specifies baseline and postrandomization variables that are considered for inclusion by the automated procedure for selecting the best models predicting the endpoint, separately for each treatment group. Interactions and variable transformations might also be considered. If predicted values for the endpoint are entered explicitly by the user, the formula can be of the form response ~ 1.
endpoint	a character string specifying the type of the response variable. The option "quantitative" (default) classifies the response as quantitative, and the mean difference is the measure of the treatment effect, whereas "dichotomous" specifies a dichotomous response, and the log odds ratio is the measure of the treatment effect. Only the first character is necessary.
data	a data frame in which to interpret the variables named in the formula, postrandom, and trt.id.
postrandom	a character vector designating postrandomization covariates included in the formula (this argument allows to distinguish baseline from postrandomiation covariates).
force.in	a vector of indices to columns of the design matrix that should be included in each regression model.
nvmax	the maximum number of covariates considered for inclusion in a model. The default is 9.
method	specifies the type of search technique used in the model selection procedure carried out by the regsubsets function. "exhaustive" (default) performs the all-subsets selection, whereas "forward" and "backward" execute a forward or backward step-wise selection, respectively.
optimal	specifies the optimization criterion for model selection. The default is "cp", Mallow's Cp, which is equivalent to AIC. The other options are "bic" for BIC and "rsq" for R-squared.
trt.id	a character string specifying the name of the treatment indicator which can be a character or a numeric vector. The control and treatment group is defined by the alphanumeric order of labels used in the treatment indicator.
conf.level	the confidence level to be used for confidence intervals reported by summary.speff.
missCtrl	estimated probabilities of observing the endpoint based on pre- and postrandomization information in the control group
missTreat	estimated probabilities of observing the endpoint based on pre- and postrandomization information in the treatment group
endCtrlPre	predicted values of the endpoint using baseline information in the control group only
endTreatPre	predicted values of the endpoint using baseline information in the treatment group only
endCtrlPost	predicted values of the endpoint using baseline and postrandomization information in the control group
endTreatPost	predicted values of the endpoint using baseline and postrandomization information in the treatment group

Details

The treatment effect is represented by the mean difference or the log odds ratio for a quantitative or dichotomous endpoint, respectively. Estimates of the treatment effect that ignore baseline covariates (naive) are included in the output.

Using the automated model selection procedure performed by regsubsets, four optimal regression models are developed for the study endpoint. Initially, all baseline and postrandomization covariates specified in the formula are considered for inclusion by the model selection procedure carried out separately in each treatment group. The optimal models are used to construct predicted values of the endpoint. Subsequently, in each treatment group, another regression model is fitted that includes only baseline covariates that were selected in the previous optimization. Then predicted values of the endpoint are computed based on these models. If missingness occurs in the endpoint variable, the model selection procedure is additionally used to determine the optimal models for predicting whether a subject has an observed endpoint, separately in each treatment group.

The function regsubsets conducts optimization of linear regression models only. The following modification in the model selection is adopted for a dichotomous variable: initially, a logistic regression model is fitted with all baseline and postrandomization covariates included in the formula. Subsequently, an optimal model is selected by using a weighted linear regression with weights from the last iteration of the IWLS algorithm. The optimal model is then refitted by logistic regression.

Besides using the built-in model selection algorithms, the user has the option to explicitly enter predicted values of the endpoint as well as estimated probabilities of observing the endpoint if it is missing at random.

Value

speff returns an object of class "speff" which can be processed by summary.speff to obtain or print a summary of the results. An object of class "speff" is a list containing the following components:

coef	a matrix with estimates of treatment-specific mean responses and the treatment effect.
cov	a list with components naive and speff, each storing the covariance matrix of the estimated treatment-specific mean responses.
varbeta	a numeric vector of variance estimates of the naive and semiparametric treatment effect estimates.
formula	a list with components control and treatment containing formula objects for the optimal selected regression models. Set to NULL if predicted values are entered explicitly.
rsq	a numeric vector of the R-squared statistics for the optimal selected regression models predicting the study endpoint. Set to NULL if predicted values are entered by the user.
endpoint	"quantitative" for a quantitative and "dichotomous" for a dichotomous response.
postrandom	a character vector of postrandomization covariates considered for selection.
predicted	a logical vector; if TRUE, the built-in model selection procedure was employed for prediction of the study endpoint in the control and treatment group, respectively.
conf.level	confidence level of the confidence intervals reported by summary.speff.
method	search technique employed in the model selection procedure.
n	number of subjects in each treatment group.

References

Robins JM, Rotnitzky A, Zhao LP. (1994), "Estimation of regression coefficients when some regressors are not always observed.", Journal of the American Statistical Association, 89:846–66.

Tsiatis AA, Davidian M, Zhang M, Lu X. (2007), "Covariate adjustment for two-sample treatment comparisons in randomized clinical trials: A principled yet flexible approach.", Statistics in Medicine, 27:4658–4677.

Zhang M, Tsiatis AA, Davidian M. (2008), "Improving efficiency of inferences in randomized clinical trials using auxiliary covariates.", Biometrics, 64:707–715.

Davidian M, Tsiatis AA, Leon S. (2005), "Semiparametric estimation of treatment effect in a pretest-posttest study with missing data.", Statistical Science, 20:261–301.

Zhang M, Gilbert P. (2009), "Increasing the efficiency of prevential trials by incorporating baseline covariates.", manuscript.

See Also

summary.speff

Examples

str(ACTG175)

### treatment effect estimation with a quantitative endpoint missing
### at random
fit1 <- speff(cd496 ~ age+wtkg+hemo+homo+drugs+karnof+oprior+preanti+
race+gender+str2+strat+symptom+cd40+cd420+cd80+cd820+offtrt, 
postrandom=c("cd420","cd820","offtrt"), data=ACTG175, trt.id="treat")

### 'fit2' adds quadratic effects of CD420 and CD820 and their 
### two-way interaction
fit2 <- speff(cd496 ~ age+wtkg+hemo+homo+drugs+karnof+oprior+preanti+
race+gender+str2+strat+symptom+cd40+cd420+I(cd420^2)+cd80+cd820+
I(cd820^2)+cd420:cd820+offtrt, postrandom=c("cd420","I(cd420^2)",
"cd820","I(cd820^2)","cd420:cd820","offtrt"), data=ACTG175, 
trt.id="treat")

### 'fit3' uses R-squared as the optimization criterion
fit3 <- speff(cd496 ~ age+wtkg+hemo+homo+drugs+karnof+oprior+preanti+
race+gender+str2+strat+symptom+cd40+cd420+cd80+cd820+offtrt, 
postrandom=c("cd420","cd820","offtrt"), data=ACTG175, trt.id="treat", 
optimal="rsq")

### a dichotomous response is created with missing values maintained
ACTG175$cd496bin <- ifelse(ACTG175$cd496 > 250, 1, 0)

### treatment effect estimation with a dichotomous endpoint missing
### at random
fit4 <- speff(cd496bin ~ age+wtkg+hemo+homo+drugs+karnof+oprior+preanti+
race+gender+str2+strat+symptom+cd40+cd420+cd80+cd820+offtrt, 
postrandom=c("cd420","cd820","offtrt"), data=ACTG175, trt.id="treat", 
endpoint="dichotomous")

speff2trial documentation built on May 31, 2022, 5:06 p.m.