Prepare comparator aggregate survival data for an unanchored indirect comparison. The comparator arm is supplied as reconstructed pseudo-IPD (event/censoring times digitized from a published Kaplan-Meier curve, e.g. via the Guyot algorithm) together with summary covariate moments (means/SDs). The Stan model integrates the comparator likelihood over the covariate distribution implied by those moments.
Usage
set_agd_surv(
data,
treatment,
Surv = NULL,
time = NULL,
status = NULL,
entry_time = NULL,
cov_means,
cov_sds = NULL,
cov_types = NULL,
study = NULL,
arm = NULL
)Arguments
- data
Data frame of reconstructed pseudo-IPD (one row per pseudo-individual).
- treatment
Column name for the (single) comparator treatment.
- Surv
Optional
survival::Surv()object describing the outcome. Use this for left/interval censoring or delayed entry.- time, status, entry_time
Character column names as an alternative to
Surv(right-censoring with status0/1, plus optional delayed entry).- cov_means
Character vector of covariate mean/proportion column names (constant within each arm). Suffixes
_mean/_propare stripped to match the IPD covariate names.- cov_sds
Character vector of covariate SD column names (
NAfor binary covariates).NULLtreats all covariates as binary.- cov_types
Character vector of
"continuous"/"binary"per covariate. IfNULL, inferred from the presence of an SD column.- study
Optional study identifier column.
- arm
Optional arm identifier column. Only a single comparator arm is supported; if supplied, it must have one unique value. Multi-arm reconstructed survival comparators are rejected until a weighting estimand is implemented. Defaults to a single arm.
Value
An object of class mlumr_agd_surv (also inheriting mlumr_agd).
The internal column names cannot be used as column names in data.
Details
Under delayed entry the comparator likelihood conditions each integration
point on survival to its entry time and then averages, so cov_means,
cov_sds and the distributions add_integration() builds must describe
the population observed at entry (those in the risk set), not a baseline
population before selection. With varying entry times that population can
differ by entry time while the model has one distribution per arm; pooled
summaries are right only under a common entry time or when the covariate
distribution among those observed at entry is the same at every entry
time. Neither condition is checkable from the summaries supplied. Delayed
entry in the individual arm is unaffected.
Reconstruction uncertainty is not propagated
The pseudo-individual records enter the likelihood as observed data, so credible intervals are conditional on this one reconstruction and narrower than the evidence supports. Treat the reconstruction as an analysis choice: digitize the curve more than once or perturb the points within their reading error, refit, and report the spread across refits beside the within-fit interval.
See also
set_agd() for non-survival aggregate data;
multinma::set_agd_surv() is the ML-NMR equivalent.