In this vignette we will demonstrate how a complex analysis function
can be constructed in order to build highly-customized tables with
`rtables`

. This example will detail the steps in creating an
analysis function to calculate a basic univariable Cox regression
summary table to analyze the treatment effect of the `ARM`

variable and any covariate/interaction effects for a survival analysis.
For a Cox regression analysis function with more customization options
and the capability of fitting multivariable Cox regression models, see
the `summarize_coxreg()`

function from the `tern`

package, which builds upon the concepts used in the construction of this
example.

The packages used in this vignette are:

example_analysis_coxreg.R

First, we prepare the data that will be used to generate a table in
this example. We will use the example `ADTTE`

(Time-To-Event
Analysis) dataset `ex_adtte`

from the `formatters`

package, which contains our treatment variable `ARM`

, several
variables that can be chosen as covariates, and censor variable
`CNSR`

from which we will derive the event variable
`EVENT`

required for our model. For the purpose of this
example, we will use age (`AGE`

) and race (`RACE`

)
as our covariates.

We prepare the data as needed to observe the desired effects in our
summary table. `PARAMCD`

is filtered so that only records of
overall survival (OS) are included, and we filter and mutate to include
only the levels of interest in our covariates. The `ARM`

variable is mutated to indicate that `"B: Placebo"`

should be
used as the reference level of our treatment variable, and the
`EVENT`

variable is derived from `CNSR`

.

```
adtte <- ex_adtte
anl <- adtte %>%
dplyr::filter(PARAMCD == "OS") %>%
dplyr::filter(ARM %in% c("A: Drug X", "B: Placebo")) %>%
dplyr::filter(RACE %in% c("ASIAN", "BLACK OR AFRICAN AMERICAN", "WHITE")) %>%
dplyr::mutate(RACE = droplevels(RACE)) %>%
dplyr::mutate(ARM = droplevels(stats::relevel(ARM, "B: Placebo"))) %>%
dplyr::mutate(EVENT = 1 - CNSR)
```

example_analysis_coxreg.R

`tidy`

Method for `summary.coxph`

Objects:
`tidy.summary.coxph`

This method allows the `tidy`

function from the
`broom`

package to operate on `summary.coxph`

output, extracting the values of interest to this analysis and returning
a tidied `tibble::tibble()`

object.

```
tidy.summary.coxph <- function(x, ...) {
is(x, "summary.coxph")
pval <- x$coefficients
confint <- x$conf.int
levels <- rownames(pval)
pval <- tibble::as_tibble(pval)
confint <- tibble::as_tibble(confint)
ret <- cbind(pval[, grepl("Pr", names(pval))], confint)
ret$level <- levels
ret$n <- x[["n"]]
ret
}
```

example_analysis_coxreg.R

`h_coxreg_inter_effect`

The `h_coxreg_inter_effect`

helper function is used within
the following helper function,
`h_coxreg_extract_interaction`

, to estimate interaction
effects from a given model for a given covariate. The function
calculates the desired statistics from the given model and returns a
`data.frame`

with label information for each row as well as
the statistics `n`

, `hr`

(hazard ratio),
`lcl`

(CI lower bound), `ucl`

(CI upper bound),
`pval`

(effect p-value), and `pval_inter`

(interaction p-value). If a numeric covariate is selected, the median
value is used as the sole “level” for which an interaction effect is
calculated. For non-numeric covariates, an interaction effect is
calculated for each level of the covariate, with each result returned on
a separate row.

```
h_coxreg_inter_effect <- function(x,
effect,
covar,
mod,
label,
control,
data) {
if (is.numeric(x)) {
betas <- stats::coef(mod)
attrs <- attr(stats::terms(mod), "term.labels")
term_indices <- grep(pattern = effect, x = attrs[!grepl("strata\\(", attrs)])
betas <- betas[term_indices]
betas_var <- diag(stats::vcov(mod))[term_indices]
betas_cov <- stats::vcov(mod)[term_indices[1], term_indices[2]]
xval <- stats::median(x)
effect_index <- !grepl(covar, names(betas))
coef_hat <- betas[effect_index] + xval * betas[!effect_index]
coef_se <- sqrt(betas_var[effect_index] + xval^2 * betas_var[!effect_index] + 2 * xval * betas_cov)
q_norm <- stats::qnorm((1 + control$conf_level) / 2)
} else {
var_lvl <- paste0(effect, levels(data[[effect]])[-1]) # [-1]: reference level
giv_lvl <- paste0(covar, levels(data[[covar]]))
design_mat <- expand.grid(effect = var_lvl, covar = giv_lvl)
design_mat <- design_mat[order(design_mat$effect, design_mat$covar), ]
design_mat <- within(data = design_mat, expr = {
inter <- paste0(effect, ":", covar)
rev_inter <- paste0(covar, ":", effect)
})
split_by_variable <- design_mat$effect
interaction_names <- paste(design_mat$effect, design_mat$covar, sep = "/")
mmat <- stats::model.matrix(mod)[1, ]
mmat[!mmat == 0] <- 0
design_mat <- apply(X = design_mat, MARGIN = 1, FUN = function(x) {
mmat[names(mmat) %in% x[-which(names(x) == "covar")]] <- 1
mmat
})
colnames(design_mat) <- interaction_names
coef <- stats::coef(mod)
vcov <- stats::vcov(mod)
betas <- as.matrix(coef)
coef_hat <- t(design_mat) %*% betas
dimnames(coef_hat)[2] <- "coef"
coef_se <- apply(design_mat, 2, function(x) {
vcov_el <- as.logical(x)
y <- vcov[vcov_el, vcov_el]
y <- sum(y)
y <- sqrt(y)
y
})
q_norm <- stats::qnorm((1 + control$conf_level) / 2)
y <- cbind(coef_hat, `se(coef)` = coef_se)
y <- apply(y, 1, function(x) {
x["hr"] <- exp(x["coef"])
x["lcl"] <- exp(x["coef"] - q_norm * x["se(coef)"])
x["ucl"] <- exp(x["coef"] + q_norm * x["se(coef)"])
x
})
y <- t(y)
y <- by(y, split_by_variable, identity)
y <- lapply(y, as.matrix)
attr(y, "details") <- paste0(
"Estimations of ", effect, " hazard ratio given the level of ", covar, " compared to ",
effect, " level ", levels(data[[effect]])[1], "."
)
xval <- levels(data[[covar]])
}
data.frame(
effect = "Covariate:",
term = rep(covar, length(xval)),
term_label = as.character(paste0(" ", xval)),
level = as.character(xval),
n = NA,
hr = if (is.numeric(x)) exp(coef_hat) else y[[1]][, "hr"],
lcl = if (is.numeric(x)) exp(coef_hat - q_norm * coef_se) else y[[1]][, "lcl"],
ucl = if (is.numeric(x)) exp(coef_hat + q_norm * coef_se) else y[[1]][, "ucl"],
pval = NA,
pval_inter = NA,
stringsAsFactors = FALSE
)
}
```

example_analysis_coxreg.R

`h_coxreg_extract_interaction`

Using the previous two helper functions,
`h_coxreg_extract_interaction`

uses ANOVA to extract
information from the given model about the given covariate. This
function will extract different information depending on whether the
effect of interest is a treatment/main effect or an interaction effect,
and returns a `data.frame`

with label information for each
row (corresponding to each effect) as well as the statistics
`n`

, `hr`

, `lcl`

, `ucl`

,
`pval`

, and `pval_inter`

(for interaction effects
only). This helper function is used directly within our analysis
function to analyze the Cox regression model and extract relevant
information to be processed and displayed within our output table.

```
h_coxreg_extract_interaction <- function(effect, covar, mod, data) {
control <- list(pval_method = "wald", ties = "exact", conf_level = 0.95, interaction = FALSE)
test_statistic <- c(wald = "Wald", likelihood = "LR")[control$pval_method]
mod_aov <- withCallingHandlers(
expr = car::Anova(mod, test.statistic = test_statistic, type = "III"),
message = function(m) invokeRestart("muffleMessage")
)
msum <- if (!any(attr(stats::terms(mod), "order") == 2)) summary(mod, conf.int = control$conf_level) else mod_aov
sum_anova <- broom::tidy(msum)
if (!any(attr(stats::terms(mod), "order") == 2)) {
effect_aov <- mod_aov[effect, , drop = TRUE]
pval <- effect_aov[[grep(pattern = "Pr", x = names(effect_aov)), drop = TRUE]]
sum_main <- sum_anova[grepl(effect, sum_anova$level), ]
term_label <- if (effect == covar) {
paste0(levels(data[[covar]])[2], " vs control (", levels(data[[covar]])[1], ")")
} else {
unname(formatters::var_labels(data, fill = TRUE)[[covar]])
}
y <- data.frame(
effect = ifelse(covar == effect, "Treatment:", "Covariate:"),
term = covar, term_label = term_label,
level = levels(data[[effect]])[2],
n = mod[["n"]], hr = unname(sum_main["exp(coef)"]), lcl = unname(sum_main[grep("lower", names(sum_main))]),
ucl = unname(sum_main[grep("upper", names(sum_main))]), pval = pval,
stringsAsFactors = FALSE
)
y$pval_inter <- NA
y
} else {
pval <- sum_anova[sum_anova$term == effect, ][["p.value"]]
## Test the interaction effect
pval_inter <- sum_anova[grep(":", sum_anova$term), ][["p.value"]]
covar_test <- data.frame(
effect = "Covariate:",
term = covar, term_label = unname(formatters::var_labels(data, fill = TRUE)[[covar]]),
level = "",
n = mod$n, hr = NA, lcl = NA, ucl = NA, pval = pval,
pval_inter = pval_inter,
stringsAsFactors = FALSE
)
## Estimate the interaction
y <- h_coxreg_inter_effect(
data[[covar]],
covar = covar,
effect = effect,
mod = mod,
label = unname(formatters::var_labels(data, fill = TRUE)[[covar]]),
control = control,
data = data
)
rbind(covar_test, y)
}
}
```

example_analysis_coxreg.R

`cached_model`

Next, we will create a helper function, `cached_model`

,
which will be used within our analysis function to cache and return the
fitted Cox regression model for the current covariate. The
`df`

argument will be directly inherited from the
`df`

argument passed to the analysis function, which contains
the full dataset being analyzed. The `cov`

argument will be
the covariate that is being analyzed depending on the current row
context. If the treatment effect is currently being analyzed, this value
will be an empty string. The `cache_env`

parameter will be an
environment object which is used to store the model for the current
covariate, also passed down from the analysis function. Of course, this
function can also be run outside of the analysis function and will still
cache and return a Cox regression model.

Using these arguments, the `cached_model`

function first
checks if a model for the given covariate `cov`

is already
stored in the caching environment `cache_env`

. If so, then
this model is retrieved and returned by `cached_model`

. If
not, the model must be constructed. This is done by first constructing
the model formula, `model_form`

, starting with only the
treatment effect (`ARM`

) and adding a covariate effect if one
is currently being analyzed. Then a Cox regression model is fit using
`df`

and the model formula, and this model is both returned
and stored in the caching environment object as
`cache_env[[cov]]`

.

```
cached_model <- function(df, cov, cache_env) {
## Check if a model already exists for
## `cov` in the caching environment
if (!is.null(cache_env[[cov]])) {
## If model already exists, retrieve it from cache_env
model <- cache_env[[cov]]
} else {
## Build model formula
model_form <- paste0("survival::Surv(AVAL, EVENT) ~ ARM")
if (length(cov) > 0) {
model_form <- paste(c(model_form, cov), collapse = " * ")
} else {
cov <- "ARM"
}
## Calculate Cox regression model
model <- survival::coxph(
formula = stats::as.formula(model_form),
data = df,
ties = "exact"
)
## Store model in the caching environment
cache_env[[cov]] <- model
}
model
}
```

example_analysis_coxreg.R

`a_cox_summary`

With our data prepared and helper function created, we can proceed to
construct our analysis function `a_cox_summary`

, which will
be used to populate all of the rows in our table. In order to be used to
generate both data rows (for interaction effects) and content rows (for
main effects), we must create a function that can be used as both
`afun`

in `analyze`

and `cfun`

in
`summarize_row_groups`

. Therefore, our function must accept
the `labelstr`

parameter.

The arguments of our analysis function will be as follows:

`df`

- a`data.frame`

of the full dataset required to fit the Cox regression model.`labelstr`

- the`string`

label for the variable being analyzed in the current row/column split context.`.spl_context`

- a`data.frame`

containing the`value`

column which is used by this analysis function to determine the name of the variable/covariate in the current split. For more details on the information stored by`.spl_context`

see`?analyze`

.`stat`

and`format`

-`string`

s that indicate which statistic column we are currently in and what format should be applied to print the statistic.`cache_env`

- an`environment`

object that can be used to store cached models so that we can prevent repeatedly fitting the same model. Instead, each model will be generated once per covariate and then reused. This argument will be passed directly to the`cached_model`

helper function we defined previously.`cov_main`

- a`logical`

value indicating whether or not the current row is summarizing covariate main effects.

The analysis function works within a given row/column split context
by using the current covariate (`cov`

) and the
`cached_model`

function to obtain the desired Cox regression
model. From this model, the `h_coxreg_extract_interaction`

function is able to extract information/statistics relevant to the
analysis and store it in a `data.frame`

. The rows in this
`data.frame`

that are of interest in the current row/column
split context are then extracted and the statistic to be printed in the
current column is retrieved from these rows. Finally, the formatted
cells with this statistic are returned as a
`VerticalRowsSection`

object. For more detail see the
commented function code below, where the purpose of each line within
`a_cox_summary`

is described.

```
a_cox_summary <- function(df,
labelstr = "",
.spl_context,
stat,
format,
cache_env,
cov_main = FALSE) {
## Get current covariate (variable used in latest row split)
cov <- tail(.spl_context$value, 1)
## If currently analyzing treatment effect (ARM) replace empty
## value of cov with "ARM" so the correct model row is analyzed
if (length(cov) == 0) cov <- "ARM"
## Use cached_model to get the fitted Cox regression
## model for the current covariate
model <- cached_model(df = df, cov = cov, cache_env = cache_env)
## Extract levels of cov to be used as row labels for interaction effects.
## If cov is numeric, the median value of cov is used as a row label instead
cov_lvls <- if (is.factor(df[[cov]])) levels(df[[cov]]) else as.character(median(df[[cov]]))
## Use function to calculate and extract information relevant to cov from the model
cov_rows <- h_coxreg_extract_interaction(effect = "ARM", covar = cov, mod = model, data = df)
## Effect p-value is only printed for treatment effect row
if (!cov == "ARM") cov_rows[, "pval"] <- NA_real_
## Extract rows containing statistics for cov from model information
if (!cov_main) {
## Extract rows for main effect
cov_rows <- cov_rows[cov_rows$level %in% cov_lvls, ]
} else {
## Extract all non-main effect rows
cov_rows <- cov_rows[nchar(cov_rows$level) == 0, ]
}
## Extract value(s) of statistic for current column and variable/levels
stat_vals <- as.list(apply(cov_rows[stat], 1, function(x) x, simplify = FALSE))
## Assign labels: covariate name for main effect (content) rows, ARM comparison description
## for treatment effect (content) row, cov_lvls for interaction effect (data) rows
nms <- if (cov_main) labelstr else if (cov == "ARM") cov_rows$term_label else cov_lvls
## Return formatted/labelled row
in_rows(
.list = stat_vals,
.names = nms,
.labels = nms,
.formats = setNames(rep(format, length(nms)), nms),
.format_na_strs = setNames(rep("", length(nms)), nms)
)
}
```

example_analysis_coxreg.R

We are able to customize our Cox regression summary using this analysis function by selecting covariates (and their labels), statistics (and their labels), and statistic formats to use when generating the output table. We also initialize a new environment object to be used by the analysis function as the caching environment to store our models in. For the purpose of this example, we will choose all 5 of the possible statistics to include in the table: n, hazard ratio, confidence interval, effect p-value, and interaction p-value.

```
my_covs <- c("AGE", "RACE") ## Covariates
my_cov_labs <- c("Age", "Race") ## Covariate labels
my_stats <- list("n", "hr", c("lcl", "ucl"), "pval", "pval_inter") ## Statistics
my_stat_labs <- c("n", "Hazard Ratio", "95% CI", "p-value\n(effect)", "p-value\n(interaction)") ## Statistic labels
my_formats <- c(
n = "xx", hr = "xx.xx", lcl = "(xx.xx, xx.xx)", pval = "xx.xxxx", pval_inter = "xx.xxxx" ## Statistic formats
)
my_env <- new.env()
ny_cache_env <- replicate(length(my_stats), list(my_env)) ## Caching environment
```

example_analysis_coxreg.R

Finally, the table layout can be constructed and used to build the desired table.

We first split our `basic_table`

using
`split_cols_by_multivar`

to ensure that each statistic exists
in its own column. To do so, we choose a variable (in this case
`STUDYID`

) which shares the same value in every row, and use
it as the split variable for every column so that the full dataset is
used to compute the model for every column. We use the
`extra_args`

argument for which each list element’s element
positions correspond to the children of (columns generated by) this
split. These arguments are inherited by all following layout elements
operating within this split, which use these elements as argument
inputs. To elaborate on this, we have three elements in
`extra_args`

: `stat`

, `format`

, and
`cache_env`

- each of which are arguments of
`a_cox_summary`

and have length equal to the number of
columns (as defined above). For each use of our analysis function
following this column split, depending on the current column context,
the corresponding element of each of these three list elements will be
inherited from `extra_args`

and used as input. For example,
if `analyze_colvars`

is called with
`a_cox_summary`

as `afun`

and is performing
calculations for column 1, `my_stats[1]`

(`"n"`

)
will be given as argument `stat`

, `my_formats[1]`

(`"xx"`

) as argument `format`

, and
`my_cache_env[1]`

(`my_env`

) as
`cache_env`

. This is useful for our table since we want each
column to print out values for a different statistic and apply its
corresponding format.

Next, we can use `summarize_row_groups`

to generate the
content row for treatment effect. This is the first instance where
`extra_args`

from the column split will be inherited and used
as argument input in `cfun`

.

After generating the treatment effect row, we want to add rows for
covariates. We use `split_rows_by_multivar`

to split rows by
covariate and apply appropriate labels.

Following this row split, we use `summarize_row_groups`

with `a_cox_summary`

as `cfun`

to generate one
content row for each covariate main effect. Once again the contents of
`extra_args`

from the column split are inherited as input.
Here we specify `cov_main = TRUE`

in the
`extra_args`

argument so that main effects rather than
interactions are considered. Since this is not a split, this instance of
`extra_args`

is not inherited by any following layout
elements. As `cov_main`

is a singular value,
`cov_main = TRUE`

will be used within every column
context.

The last part of our table is the covariate interaction effects. We
use `analyze_colvars`

with `a_cox_summary`

as
`afun`

, and again inherit `extra_args`

from the
column split. Using an `rtables`

“analyze” function generates
data rows, with one row corresponding to each covariate level (or median
value, for numeric covariates), nested under the content row (main
effect) for that same covariate.

```
lyt <- basic_table() %>%
## Column split: one column for each statistic
split_cols_by_multivar(
vars = rep("STUDYID", length(my_stats)),
varlabels = my_stat_labs,
extra_args = list(
stat = my_stats,
format = my_formats,
cache_env = ny_cache_env
)
) %>%
## Create content row for treatment effect
summarize_row_groups(cfun = a_cox_summary) %>%
## Row split: one content row for each covariate
split_rows_by_multivar(
vars = my_covs,
varlabels = my_cov_labs,
split_label = "Covariate:",
indent_mod = -1 ## Align split label left
) %>%
## Create content rows for covariate main effects
summarize_row_groups(
cfun = a_cox_summary,
extra_args = list(cov_main = TRUE)
) %>%
## Create data rows for covariate interaction effects
analyze_colvars(afun = a_cox_summary)
```

example_analysis_coxreg.R

Using our pre-processed `anl`

dataset, we can now build
and output our final Cox regression summary table.

```
cox_tbl <- build_table(lyt, anl)
cox_tbl
#> p-value p-value
#> n Hazard Ratio 95% CI (effect) (interaction)
#> ————————————————————————————————————————————————————————————————————————————————————————————————
#> A: Drug X vs control (B: Placebo) 247 0.97 (0.71, 1.32) 0.8243
#> Covariate:
#> Age 247 0.7832
#> 34 0.92 (0.68, 1.26)
#> Race 247 0.7441
#> ASIAN 1.03 (0.68, 1.57)
#> BLACK OR AFRICAN AMERICAN 0.78 (0.41, 1.49)
#> WHITE 1.06 (0.55, 2.04)
```

example_analysis_coxreg.R