Network Meta-Analysis to Predict the Efficacy of an Approved Treatment in a New Indication
These files allow the user to replicate the simulation study in the above paper. They also demonstrate how to apply the proposed methods to a data set in practice.
These functions can be used to:
- Randomly generate a set of indication-specific basic parameters using a desired amount of correlation.
- Randomly generate a data set with binary outcomes according to a user-specified network.
- Fit a standard contrast-based NMA model to data from each indication.
- Fit the proposed NMA models for 2 indications to a given data set.
- Compute summary statistics (Bias, variance, RMSE, average width of the 95% credible interval, and coverage probability).
- Compute probability of success for a future clinical trial.
The purpose, inputs, and outputs of each function are included in this R script.
This R script demonstrates how to use the functions in NMA-Simulation-Functions.R to replicate the simulation study described in Section 5.1 of the paper. In particular, the R object "Mixed.Mod.Trt2.Corr5" will contain the posterior samples for
In addition, this file demonstrates how to apply the proposed methodology in practice, including how to compute PoS for our Motivating Example using the file pso-psa-data.csv [Section 6 of the manuscript]. The data contained in pso-psa-data.csv was curated from publicly available data for multi-arm trials in psoriasis and psoriatic arthritis. For more information, please see Section 2 of the manuscript.
This folder contains the Jags scripts required to implement each standard CB-NMA model and each proposed NMA model for 2 indications.
This CSV file contains the dataset that was used in our motivating example. This dataset has been de-identified for confidentiality reasons.
This is a lock file produced by the Rpackage 'renv' that allows users to run our code using the same package versions.