In the psrwe, PS-integrated Kaplan-Meier (PSKM) method (Chen, et al., 2022) is also implemented for leveraging real-world evidence in augmenting single-arm studies. The PSKM is an non-parametric approach for evaluating time-to-event endpoints.
Similar with the approaches: PSPP (Wang, et al., 2019) and PSCL
(Wang, et al., 2020), the PS-integrated study design functions,
psrwe_est() and psrwe_borrow(), below estimate
PS model, set borrowing parameters, and determine discounting parameters
for borrowing information.
data(ex_dta)
dta_ps <- psrwe_est(ex_dta,
v_covs = paste("V", 1:7, sep = ""),
v_grp = "Group",
cur_grp_level = "current",
nstrata = 5,
ps_method = "logistic")
ps_bor <- psrwe_borrow(dta_ps,
total_borrow = 30,
method = "distance")For single arm studies, when there is one external data source, the
function psrwe_survkm() allows one to conduct the survival
analysis via Kaplan-Meier (KM) estimates (Kaplan and Meier, 1985). The
PSKM approach is applied in each PS stratum to obtain stratum-specific
KM estimates on all distinctive time points, which are combined to
complete the overall survival estimates. Suppose we are interested in
the survival probability at one year, then we may use the argument
pred_tp=365 (days) in the function
psrwe_survkm() to specify the time point of interest.
## With a total of 30 subject borrowed from the RWD, based on
## the survival probability at time 365, the point estimate is
## 0.779 with standard error 0.027.
The pred_tp_365 will be carried on to other down-stream
analyses. However, the function psrwe_survkm() still
returns results on all distinctive time points which may be also needed
for down-stream analysis (e.g., visualizing KM curves and confidence
intervals). Therefore, the returned object rst_km above may
have different data structure then those returned by the PSPP and PSCL
approaches. Please use str() to see the details.
The default method of stderr_method for KM estimates is
based on the Greenwood formula and the asymptotic theorem that may rely
on the independent assumption. However, the Jackknife may provide more
robust estimations for the standard errors in general.
Two Jackknife options have been implemented for estimating standard
errors of the survival estimates via the options for the function
psrwe_survkm(): * stderr_method = "jk" applies
Jackknife by each stratum. * stderr_method = "sjk" applies
simple Jackknife on the overall survival probability. Both results may
be similar but slightly different since the overall weights are fixed
and close to one over the number of total strata.
Please see Section of Demo example below for examples using
stderr_method.
The overall survival estimates can be further visualized as below.
The stratum-specific survival estimates can be further visualized as below.
The confidence intervals can be also visualized as below.
The inference for the parameters of interest such as survival
probability or rate at one year (pred_tp=365 days) can be
further arrived from the utility function psrwe_outana().
For example, the code below test the one year survival probability is
greater than mu = 0.7 (i.e., 70%)
or not, i.e., the example tests \[
H_0: S(\tau) \leq 0.7 \quad \mbox{vs.} \quad H_a: S(\tau) > 0.7
\] where \(S(\tau)\) is the
survival probability at time \(\tau =
365\) days.
## - Method: ps_km, Outcome Type: tte, Study Type: single-arm
## - Predict Time Point: 365
## - StdErr Method: naive
## - Interval Method: wald, Level: 0.95, Type: log_log
## - Test Method: p_value, Method pval: wald
## H0: theta <= 0.700 vs. Ha: theta > 0.700
## - Analysis Results:
## Stratum Mean StdErr T Lower Upper p.value
## Overall 0.779 0.0272 365 0.72 0.827 0.00192
The details of stratum-specific estimates can be printed via the
print() function with the option
show_details = TRUE.
## - Method: ps_km, Outcome Type: tte, Study Type: single-arm
## - Predict Time Point: 365
## - StdErr Method: naive
## - Interval Method: wald, Level: 0.95, Type: log_log
## - Test Method: p_value, Method pval: wald
## H0: theta <= 0.700 vs. Ha: theta > 0.700
## - Analysis Results:
## Stratum Mean StdErr T Lower Upper p.value
## Stratum 1 0.830 0.0590 365 0.675 0.916 1.35e-02
## Stratum 2 0.776 0.0617 365 0.626 0.872 1.09e-01
## Stratum 3 0.608 0.0744 365 0.447 0.736 8.91e-01
## Stratum 4 0.760 0.0636 365 0.607 0.860 1.73e-01
## Stratum 5 0.918 0.0407 365 0.790 0.970 3.98e-08
## Overall 0.779 0.0272 365 0.720 0.827 1.92e-03
As the survival package, the results of other time
points can be also predicted via the summary() with the
option pred_tps.
## - Method: ps_km, Outcome Type: tte, Study Type: single-arm
## - Predict Time Point: 180 365
## - StdErr Method: naive
## - Interval Method: wald, Level: 0.95, Type: log_log
## - Test Method: p_value, Method pval: wald
## H0: theta <= 0.700 vs. Ha: theta > 0.700
## - Analysis Results:
## Stratum Mean StdErr T Lower Upper p.value
## Overall 0.900 0.0192 180 0.855 0.931 1.02e-25
## Overall 0.779 0.0272 365 0.720 0.827 1.92e-03
The script in “psrwe/demo/sec_4_4_ex.r” source file
has the full example for the PSKM single-arm study which can be run via
the demo("sec_4_4_ex", package = "psrwe").
Two Jackknife standard errors are also demonstrated in the script.
Note that Jackknife standard errors may take a while to finish.
Kaplan, E. L. and Meier, P. (1958). Nonparametric Estimation from Incomplete Observations. Journal of the American Statistical Association, 53(282), 457-481.
Chen, W.-C., Lu, N., Wang, C., Li, H., Song, C., Tiwari, R., Xu, Y., and Yue, L.Q. (2022). Propensity Score-Integrated Approach to Survival Analysis: Leveraging External Evidence in Single-Arm Studies. Journal of Biopharmaceutical Statistics, 32(3), 400-413.
Wang, C., Li, H., Chen, W. C., Lu, N., Tiwari, R., Xu, Y., and Yue, L.Q. (2019). Propensity score-integrated power prior approach for incorporating real-world evidence in single-arm clinical studies. Journal of Biopharmaceutical Statistics, 29(5), 731-748.
Wang, C., Lu, N., Chen, W. C., Li, H., Tiwari, R., Xu, Y., and Yue, L.Q. (2020). Propensity score-integrated composite likelihood approach for incorporating real-world evidence in single-arm clinical studies. Journal of Biopharmaceutical Statistics, 30(3), 495-507.