Objective

To compare the clinical effectiveness of a MET inhibitor for NSCLC with MET exon 14 skipping mutation against relevant comparator treatments using an IPD-based MAIC

Methods

  • Conducted an unanchored matching-adjusted indirect comparison (MAIC) in R using individual patient-level data (IPD) from a single clinical trial
  • Reweighted IPD to align with published baseline characteristics of comparator studies
  • Performed survival analyses on the adjusted dataset, with sensitivity analyses to assess robustness and residual uncertainty

Outcome

Delivered a credible, decision-grade comparative effectiveness assessment to support client decision-making and strategic planning

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