| Type: | Package |
| Title: | Assessing Cure Model Appropriateness for Survival Data |
| Version: | 0.1.0 |
| Description: | Assesses whether cure models are appropriate for right-censored survival data, where a fraction of subjects may never experience the event of interest. Implements a two-stage workflow combining Kaplan-Meier visualization and comparison of parametric cure and non-cure models by the Akaike information criterion with formal diagnostics for sufficient follow-up and for the presence of a cured fraction. The diagnostics include the statistics of Maller and Zhou (1992) <doi:10.1093/biomet/79.4.731> and Maller and Zhou (1994) <doi:10.1080/01621459.1994.10476889>, the test of Shen (2000) <doi:10.1016/S0167-7152(00)00063-8>, and the ratio estimation of censored uncured subjects ('RECeUS') method of Selukar and Othus (2023) <doi:10.1002/sim.9610>. |
| License: | MIT + file LICENSE |
| URL: | https://github.com/GeethanjaleeM/cureAssess |
| BugReports: | https://github.com/GeethanjaleeM/cureAssess/issues |
| Encoding: | UTF-8 |
| Language: | en-US |
| Depends: | R (≥ 4.1.0) |
| Imports: | survival, flexsurv, flexsurvcure, survminer, ggplot2, dplyr, stats |
| Suggests: | knitr, rmarkdown, testthat (≥ 3.0.0) |
| Config/testthat/edition: | 3 |
| VignetteBuilder: | knitr |
| Config/roxygen2/version: | 8.1.0 |
| NeedsCompilation: | no |
| Packaged: | 2026-09-02 19:48:52 UTC; durbadal |
| Author: | Geethanjalee Mudunkotuwa [aut, cre, cph], Durbadal Ghosh [aut] |
| Maintainer: | Geethanjalee Mudunkotuwa <geethanjaleem@gmail.com> |
| Repository: | CRAN |
| Date/Publication: | 2026-09-14 15:50:02 UTC |
cureAssess: Assessing Cure Model Appropriateness for Survival Data
Description
Tools for deciding whether a cure model is appropriate for right-censored survival data, that is, whether the data plausibly contain a fraction of subjects who will never experience the event of interest.
Details
The package implements a two-stage workflow.
Stage 1 – screening. prepare.surv.data() standardizes a data frame
into the survival time (Y) and event indicator (D) columns used
throughout the package. model.fitting() then fits matched cure and
non-cure parametric models and ranks them by AIC. If the smallest-AIC model
is a cure model, that is initial support for cure modeling.
Stage 2 – diagnostics. run.cure.tests() applies the formal
diagnostics: mz.test() and qn.test() (Maller-Zhou statistics for
sufficient follow-up), shen.test() (Shen's test), immune.test() (a
descriptive summary of the tail of the Kaplan-Meier curve), and
receus.method() (the RECeUS ratio of censored uncured subjects).
cure.appropriateness() runs both stages and returns a single object with
print() and summary() methods.
Diagnostics for sufficient follow-up ask whether the study ran long enough to distinguish a genuine cure fraction from a plateau caused by censoring. They are descriptive aids and should be read together, and alongside subject-matter knowledge, rather than treated as a single decision rule.
Author(s)
Maintainer: Geethanjalee Mudunkotuwa geethanjaleem@gmail.com [copyright holder]
Authors:
Geethanjalee Mudunkotuwa geethanjaleem@gmail.com [copyright holder]
Durbadal Ghosh reevu7@gmail.com
References
Maller RA, Zhou S (1992). Estimating the proportion of immunes in a censored sample. Biometrika, 79(4), 731–739. doi:10.1093/biomet/79.4.731
Maller RA, Zhou S (1994). Testing for sufficient follow-up and outliers in survival data. Journal of the American Statistical Association, 89(428), 1499–1506. doi:10.1080/01621459.1994.10476889
Shen P-S (2000). Testing for sufficient follow-up in survival data. Statistics & Probability Letters, 49(4), 313–322. doi:10.1016/S0167-7152(00)00063-8
Selukar S, Othus M (2023). RECeUS: Ratio estimation of censored uncured subjects, a different approach for assessing cure model appropriateness in studies with long-term survivors. Statistics in Medicine, 42(3), 209–227. doi:10.1002/sim.9610
See Also
Useful entry points:
cure.appropriateness,
prepare.surv.data,
model.fitting,
run.cure.tests
Validate survival data input
Description
Internal helper to validate that the input data frame contains
survival time and event indicator columns named Y and D.
Usage
.check_surv_data(data)
Arguments
data |
A data frame containing survival data. |
Value
Invisibly returns TRUE if checks pass.
Map fitted model names to RECeUS distribution codes
Description
Internal helper to convert model names from the AIC table into
the distribution codes used by receus.method().
Usage
.map_model_to_receus_dist(model_name)
Arguments
model_name |
Character string. |
Value
A character string giving the RECeUS distribution code.
Assess cure model appropriateness in two stages
Description
Performs a two-stage workflow for cure model assessment.
Usage
cure.appropriateness(
data,
time,
status,
time_scale = c("none", "days_to_years"),
dist = NULL,
plot_km = TRUE,
run_tests = c("auto", "yes", "no"),
include_lognormal = FALSE
)
Arguments
data |
A data frame. |
time |
Character string giving the survival time column name. |
status |
Character string giving the event indicator column name. |
time_scale |
Either |
dist |
Optional distribution to use for the RECeUS method.
If |
plot_km |
Logical; if |
run_tests |
One of |
include_lognormal |
Logical; passed to |
Details
Stage 1:
Prepares the data
Fits a Kaplan-Meier curve
Fits candidate cure and non-cure models
Compares them using AIC
Selects the model with the smallest AIC
Provides an initial recommendation
Stage 2:
Runs cure-appropriateness tests such as Maller-Zhou statistics, Shen's test, immune summaries and RECeUS-style outputs.
If the smallest-AIC model is a non-cure model, the function reports that a cure model is not supported by the initial model-comparison step, while still allowing the user to proceed with additional tests if desired.
Value
An object of class "cure.appropriateness" containing:
- data
The standardized survival dataset returned by
prepare.surv.data(), containing the survival time (Y) and event indicator (D).- screening
A list containing results from the model screening step.
- screening$kmfit
Kaplan-Meier estimate of the survival function (
survival::survfitobject).- screening$kmplot
Kaplan-Meier plot generated using
survminer::ggsurvplot, returned whenplot_km = TRUE.- screening$aic_table
A data frame summarizing the fitted candidate models, including model name, model type (
"cure"or"non-cure"), AIC value, and parameter estimates.- screening$best_model
The model with the smallest AIC.
- screening$best_model_type
Indicates whether the best model is a
"cure"or"non-cure"model.- screening$initial_decision
Text summarizing the initial interpretation based on the AIC comparison.
- selected_receus_model
The cure model selected for the RECeUS method, based on the smallest AIC among cure models.
- selected_receus_dist
The distribution code used by the RECeUS procedure.
- tests
A list containing results from additional cure-appropriateness diagnostics.
- tests_run
Logical indicator specifying whether additional diagnostic tests were executed.
- tests_reason
Explanation describing why the diagnostic tests were or were not executed.
- final_recommendation
A text summary combining the screening results and optional diagnostic tests to provide a final interpretation regarding cure model appropriateness.
See Also
prepare.surv.data,
model.fitting,
run.cure.tests
Examples
library(survival)
# Stage 1 only: Kaplan-Meier screening and AIC model comparison
res <- cure.appropriateness(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years",
plot_km = FALSE,
run_tests = "no"
)
res
# Stage 1 and Stage 2: also run the cure-appropriateness diagnostics
res_full <- cure.appropriateness(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years",
plot_km = FALSE,
run_tests = "yes"
)
summary(res_full)
Compute immune-related summary quantities
Description
Computes Kaplan-Meier-based summary quantities used to assess whether right-censored survival data may contain a subgroup of long-term survivors (sometimes referred to as "immune" or "cured" individuals).
Usage
immune.test(dat)
Arguments
dat |
A data frame containing columns |
Details
The method evaluates the behavior of the Kaplan-Meier survival curve at the end of follow-up. In particular, it considers:
the estimated event probability by the end of follow-up,
the proportion of censored observations, and
whether the largest observed follow-up time corresponds to a censored observation.
If the largest observed time is censored and the Kaplan-Meier curve appears to level off above zero, this is consistent with the presence of a survival plateau and may suggest a cure fraction. In contrast, if the largest observed time is an event, the evidence for a survival plateau is weaker.
This function provides a descriptive summary rather than a formal hypothesis test and is intended to be interpreted together with other diagnostics such as the Maller-Zhou test, qn statistic, Shen test, and RECeUS method.
Value
An object of class "immune.test.result" containing:
- method
Name of the diagnostic summary.
- p_hat
Estimated event probability by the end of follow-up, derived from the Kaplan-Meier curve.
- p_cens
Observed proportion of censored observations.
- last_observation
Largest observed follow-up time.
- last_observation_censored
Logical indicator of whether the largest observed follow-up time is censored.
- interpretation
Text describing the implication of the summary quantities for the presence of a survival plateau and possible cure fraction.
References
Maller RA, Zhou S (1992). Estimating the proportion of immunes in a censored sample. Biometrika, 79(4), 731–739. doi:10.1093/biomet/79.4.731
Maller RA, Zhou S (1994). Testing for sufficient follow-up and outliers in survival data. Journal of the American Statistical Association, 89(428), 1499–1506. doi:10.1080/01621459.1994.10476889
Maller RA, Zhou S (1995). Testing for the presence of immune or cured individuals. Biometrics, 51, 1197–1205. doi:10.2307/2533253
Maller RA, Zhou X (1996). Survival Analysis with Long-term Survivors. Wiley.
Examples
library(survival)
dat <- prepare.surv.data(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years"
)
res <- immune.test(dat)
res
Internal maximum likelihood wrapper
Description
Internal helper used by RECeUS-style calculations.
Usage
mleFun(dat, dist = "exp")
Arguments
dat |
A data frame with columns |
dist |
Distribution name. |
Value
A named numeric vector.
Fit candidate cure and non-cure survival models
Description
Fits a set of parametric survival models and corresponding cure models to right-censored survival data, compares them using the Akaike Information Criterion (AIC), and identifies the model with the smallest AIC.
Usage
model.fitting(data, plot_km = TRUE, include_lognormal = FALSE)
Arguments
data |
A data frame containing columns |
plot_km |
Logical; if |
include_lognormal |
Logical; if |
Details
The default candidate distributions are exponential, Weibull, gamma, and
log-logistic, matching the four distributions used in the tutorial worked
example. The lognormal distribution is available as an optional addition via
include_lognormal = TRUE.
For each distribution, both a non-cure model and a cure model are fitted. A Kaplan-Meier estimate is also computed, and a Kaplan-Meier plot can be optionally returned.
Value
An object of class "cure.model.fit" containing:
- kmfit
A
survival::survfitobject representing the Kaplan-Meier estimate of the survival function.- kmplot
A Kaplan-Meier plot object created using
survminer::ggsurvplot. This is returned only whenplot_km = TRUE.- fits
A named list of fitted model results. Each element contains:
- fit
The fitted model object, or
NULLif fitting failed.- AIC
The Akaike Information Criterion value for the fitted model.
- error
An error message if model fitting failed, otherwise
NULL.
- aic_table
A data frame summarizing the fitted models, including model name, model type (
"cure"or"non-cure"), AIC value, parameter estimates, and fitting errors. The table is ordered by increasing AIC.- best_model
A character string giving the name of the model with the smallest AIC.
- best_model_type
A character string indicating whether the best model is a
"cure"or"non-cure"model.
Objects of class "cure.model.fit" represent the model-screening stage of
cure model assessment and are typically used as input for downstream
functions such as run.cure.tests() and cure.appropriateness().
See Also
prepare.surv.data,
run.cure.tests,
cure.appropriateness,
print.cure.model.fit,
summary.cure.model.fit,
plot.cure.model.fit
Examples
library(survival)
dat <- prepare.surv.data(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years"
)
fit_res <- model.fitting(dat, plot_km = FALSE)
fit_res$aic_table
fit_res$best_model
fit_res$best_model_type
Compute the Maller-Zhou test statistic
Description
Computes the Maller-Zhou test statistic used to assess whether a cure fraction may exist in right-censored survival data. The test is based on examining the behavior of events near the end of follow-up.
Usage
mz.test(dat, alpha = 0.05)
Arguments
dat |
A data frame containing columns |
alpha |
Significance level used for interpretation. Default is |
Details
The key idea is that if a cure fraction exists, the Kaplan-Meier survival curve will eventually reach a plateau above zero because a subset of individuals will never experience the event. In contrast, if no cure fraction exists, events should continue to occur toward the end of follow-up.
The Maller-Zhou statistic evaluates the number of events occurring in a time window near the largest observed event time. If relatively few events occur in this region, it provides evidence consistent with the presence of a cure fraction.
The test can only be computed when the largest observed time corresponds to a censored observation (i.e., follow-up extends beyond the last event).
Value
An object of class "cure.test.result" containing:
- method
Name of the test.
- statistic
Computed Maller-Zhou statistic.
- alpha
Significance level used for interpretation.
- interpretation
Text describing the implication of the test result for the presence of a cure fraction.
References
Maller RA, Zhou S (1992). Estimating the proportion of immunes in a censored sample. Biometrika, 79(4), 731–739. doi:10.1093/biomet/79.4.731
Maller RA, Zhou S (1994). Testing for sufficient follow-up and outliers in survival data. Journal of the American Statistical Association, 89(428), 1499–1506. doi:10.1080/01621459.1994.10476889
Maller RA, Zhou X (1996). Survival Analysis with Long-Term Survivors. Wiley.
Examples
library(survival)
dat <- prepare.surv.data(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years"
)
res <- mz.test(dat)
res
Plot a fitted cure model object
Description
Displays the Kaplan-Meier plot stored in a cure.model.fit object.
Usage
## S3 method for class 'cure.model.fit'
plot(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments passed to other methods. |
Value
The input object x, returned invisibly.
Examples
library(survival)
dat <- prepare.surv.data(gbsg, "rfstime", "status", "days_to_years")
fit_res <- model.fitting(dat, plot_km = TRUE)
plot(fit_res)
Prepare survival data for cure model assessment
Description
Standardizes survival data into a format required by the package.
The returned data frame always contains columns Y for survival time
and D for event indicator, D = 1 for event and D = 0 for censoring.
Usage
prepare.surv.data(data, time, status, time_scale = c("none", "days_to_years"))
Arguments
data |
A data frame. |
time |
Character string giving the survival time column name. |
status |
Character string giving the event indicator column name. |
time_scale |
Either |
Value
A data frame with standardized columns Y for survival time
and D for event indicator, D = 1 for event and D = 0 for censoring.
See Also
model.fitting,
cure.appropriateness
Examples
library(survival)
# `rfstime` is recorded in days, so convert it to years
dat <- prepare.surv.data(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years"
)
head(dat[, c("Y", "D")])
Print cure model appropriateness analysis results
Description
Prints a summary of a cure.appropriateness object, including the
screening results, RECeUS model selection, testing status, and
final recommendation.
Usage
## S3 method for class 'cure.appropriateness'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments passed to other methods. |
Value
The input object x, returned invisibly.
Print a fitted cure model object
Description
Prints a summary of a cure.model.fit object, including the best
model identified by AIC and the full AIC comparison table.
Usage
## S3 method for class 'cure.model.fit'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments passed to other methods. |
Value
The input object x, returned invisibly.
Print cure model test results
Description
Prints the results of a cure model diagnostic test, including the test statistic, significance level (if available), and interpretation.
Usage
## S3 method for class 'cure.test.result'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments passed to other methods. |
Value
The input object x, returned invisibly.
Print immune test results
Description
Prints the results of the immune-based cure model diagnostic test, including estimated proportions and censoring information.
Usage
## S3 method for class 'immune.test.result'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments passed to other methods. |
Value
The input object x, returned invisibly.
Print RECeUS cure model assessment results
Description
Prints the results from a RECeUS-based cure model assessment, including the estimated cure fraction, remaining uncured ratio, and the decision regarding cure model appropriateness.
Usage
## S3 method for class 'receus.output'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments passed to other methods. |
Value
The input object x, returned invisibly.
Print a summary of cure model appropriateness results
Description
Prints the condensed summary produced by
summary.cure.appropriateness(), including the best model identified
during screening, the AIC comparison table, whether diagnostic tests were
run, and the final recommendation.
Usage
## S3 method for class 'summary.cure.appropriateness'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments passed to other methods. |
Value
The input object x, returned invisibly.
Compute the qn statistic
Description
Computes the qn statistic proposed by Maller and Zhou (1996), which is a descriptive diagnostic used to assess whether follow-up is sufficient to detect a survival plateau in right-censored survival data. A survival plateau may indicate the presence of a cure fraction, meaning that a subset of individuals will never experience the event of interest.
Usage
qn.test(dat)
Arguments
dat |
A data frame containing columns |
Details
The statistic is qn = Nn / n, where Nn is the number of events falling in
the late-time window (2*Y* - Y_max, Y*], Y* is the largest event time, and
Y_max is the largest observed time. The width of this window equals the gap
Y_max - Y* between the last event and the end of follow-up. A long plateau
(sufficient follow-up) produces a wide window that captures many events, so
larger values of qn indicate stronger evidence of sufficient follow-up
and a survival plateau. Smaller values indicate that events continue up to
the end of follow-up, providing weaker evidence for a plateau.
For a formal decision, this implementation uses the companion Maller-Zhou
statistic alpha_n = (1 - qn)^n (Maller & Zhou 1994, their eq. 5):
sufficient follow-up is supported when alpha_n < 0.05, equivalently when
qn exceeds 1 - 0.05^(1/n) (a threshold that depends on the sample size
n). Note this alpha_n-equivalent rule is the same decision used by
mz.test(); the exact finite-sample critical values for qn derived by
Maller, Resnick and Shemehsavar (2024) are not implemented here. The qn
statistic itself is reported and is directionally informative regardless of
the cutoff used.
The statistic can only be computed when the largest observed follow-up time is a censored observation (i.e., follow-up extends beyond the last event).
Value
An object of class "cure.test.result" containing:
- method
Name of the statistic.
- statistic
Computed qn statistic.
- interpretation
Text describing the implication of the statistic for the presence of a survival plateau and possible cure fraction.
References
Maller RA, Resnick S, Shemehsavar S (2024). Finite sample and asymptotic distributions of a statistic for sufficient follow-up in cure models. Canadian Journal of Statistics, 52(2), 359–379. doi:10.1002/cjs.11771
Maller RA, Zhou S (1992). Estimating the proportion of immunes in a censored sample. Biometrika, 79(4), 731–739. doi:10.1093/biomet/79.4.731
Maller RA, Zhou S (1994). Testing for sufficient follow-up and outliers in survival data. Journal of the American Statistical Association, 89(428), 1499–1506. doi:10.1080/01621459.1994.10476889
Maller RA, Zhou X (1996). Survival Analysis with Long-term Survivors. Wiley.
Examples
library(survival)
dat <- prepare.surv.data(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years"
)
res <- qn.test(dat)
res
Internal ratio test helper
Description
Internal ratio test helper
Usage
ratioTest(dat, whichTau, dist = "exp")
Arguments
dat |
A data frame with columns |
whichTau |
Evaluation time point. |
dist |
Distribution name. |
Value
A numeric vector of estimates.
Compute RECeUS cure model diagnostic outputs
Description
Computes cure-fraction-related summary quantities using a selected parametric survival model and evaluates cure model appropriateness using the RECeUS method proposed by Selukar and Othus (2023).
Usage
receus.method(data, dist = "exp", whichTau = NULL)
Arguments
data |
A data frame containing columns |
dist |
Character string specifying the parametric model used in the RECeUS calculation. Supported values are:
|
whichTau |
Optional evaluation time. If |
Details
The RECeUS method is based on two quantities:
-
pi_hat: the estimated cure fraction -
r_hat: the estimated proportion of uncured subjects remaining censored at the end of follow-up
This diagnostic is typically applied after model screening when a
cure model is selected as the preferred model based on information
criteria such as AIC (e.g., "exp", "wei",
"llogis", "gam", "lnorm"). However, the method can also be
applied using non-cure parametric models.
When a non-cure model is used (e.g., "expUnc", "weiUnc",
"llogisUnc", "gamUnc", "lnormUnc"), the cure fraction is
constrained to zero by the model specification. In this case the
method will always return:
-
pi_hat = 0 -
r_hat = 1
A cure model is considered appropriate when both of the following conditions are satisfied:
-
pi_hat > 0.025 -
r_hat < 0.05
The first condition indicates that the estimated cure fraction is meaningfully greater than zero, while the second condition indicates that only a small proportion of uncured subjects remain censored at the end of follow-up. Together, these conditions suggest both the presence of a cure fraction and sufficient follow-up for reliable cure model estimation.
This function can be applied using either cure or non-cure parametric
model specifications, depending on the value of dist.
Value
An object of class "receus.output" containing:
- method
Name of the diagnostic procedure.
- dist
Distribution used in the RECeUS calculation.
- tau
Evaluation time used in the calculation.
- estimates
Raw vector of estimated model quantities returned by the internal RECeUS calculation.
- pi_hat
Estimated cure fraction.
- r_hat
Estimated proportion of uncured subjects remaining censored at the end of follow-up.
- cure_fraction_condition
Logical indicator of whether
pi_hat > 0.025.- followup_condition
Logical indicator of whether
r_hat < 0.05.- decision
Text summary of whether the RECeUS criteria support cure model appropriateness.
- interpretation
Text describing the implication of the RECeUS quantities for cure model appropriateness and sufficiency of follow-up.
References
Selukar S, Othus M (2023). RECeUS: Ratio estimation of censored uncured subjects. Statistics in Medicine, 42(3), 209–227. doi:10.1002/sim.9610
Examples
library(survival)
dat <- prepare.surv.data(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years"
)
res <- receus.method(dat, dist = "lnorm")
res
Run cure model appropriateness diagnostics
Description
Runs a set of diagnostic procedures used to assess whether a cure model may be appropriate for right-censored survival data. The diagnostics include the Maller-Zhou test, qn statistic, Shen test, immune summary, and RECeUS method.
Usage
run.cure.tests(data, dist = NULL)
Arguments
data |
A data frame containing columns |
dist |
Character string giving the distribution to be used for the
RECeUS method. If |
Value
An object of class "cure.tests" containing:
- mz
Result of the Maller-Zhou diagnostic test.
- qn
Result of the qn statistic.
- shen
Result of Shen's test.
- immune
Result of the immune summary diagnostic.
- receus
Result of the RECeUS method.
Examples
library(survival)
dat <- prepare.surv.data(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years"
)
res <- run.cure.tests(dat, dist = "lnorm")
res$mz
res$receus
Compute Shen's test statistic
Description
Computes the Shen (2000) diagnostic test statistic used to assess whether follow-up in right-censored survival data is sufficient to detect a potential cure fraction.
Usage
shen.test(dat, alpha = 0.05)
Arguments
dat |
A data frame containing columns |
alpha |
Significance level used for interpretation. Default is |
Details
The test examines the pattern of events near the end of follow-up. If a cure fraction exists, the Kaplan-Meier survival curve will tend to flatten (plateau) because a subset of individuals will never experience the event of interest. In contrast, if no cure fraction exists, events should continue to occur late in follow-up and the survival curve will continue to decline.
Shen's test evaluates whether the number of events occurring in a late follow-up interval is consistent with the presence of such a plateau. Smaller values of the test statistic provide stronger evidence supporting the presence of a cure fraction.
The test can only be computed when the largest observed follow-up time corresponds to a censored observation (i.e., follow-up extends beyond the last observed event time).
Value
An object of class "cure.test.result" containing:
- method
Name of the diagnostic test.
- statistic
Computed Shen test statistic.
- alpha
Significance level used for interpretation.
- interpretation
Text describing the implication of the statistic for the presence of a survival plateau and possible cure fraction.
References
Shen P-S (2000). Testing for sufficient follow-up in survival data. Statistics & Probability Letters, 49(4), 313–322. doi:10.1016/S0167-7152(00)00063-8
Examples
library(survival)
dat <- prepare.surv.data(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years"
)
res <- shen.test(dat)
res
Summarize cure model appropriateness results
Description
Returns a summary of a cure.appropriateness object, including
the best model identified during screening, the AIC comparison
table, tests performed, and the final recommendation.
Usage
## S3 method for class 'cure.appropriateness'
summary(object, ...)
Arguments
object |
An object of class |
... |
Additional arguments passed to other methods. |
Value
An object of class "summary.cure.appropriateness"
containing key results from the cure model appropriateness analysis.
Examples
library(survival)
res <- cure.appropriateness(
data = gbsg,
time = "rfstime",
status = "status",
time_scale = "days_to_years",
plot_km = FALSE,
run_tests = "no"
)
summary(res)
Summarize a fitted cure model object
Description
Returns the AIC comparison table from a cure.model.fit object.
Usage
## S3 method for class 'cure.model.fit'
summary(object, ...)
Arguments
object |
An object of class |
... |
Additional arguments passed to other methods. |
Value
A data frame containing the AIC comparison of candidate models.
Examples
library(survival)
dat <- prepare.surv.data(gbsg, "rfstime", "status", "days_to_years")
fit_res <- model.fitting(dat, plot_km = FALSE)
summary(fit_res)