Addressing challenges with real-world synthetic control arms to demonstrate the comparative effectiveness of Pralsetinib in non-small cell lung cancer.
Sanjay PopatStephen V LiuNicolas ScheuerGrace G HsuAlexandre LockhartSreeram V RamagopalanFrank GriesingerVivek SubbiahPublished in: Nature communications (2022)
As advanced non-small cell lung cancer (aNSCLC) is being increasingly divided into rare oncogene-driven subsets, conducting randomised trials becomes challenging. Using real-world data (RWD) to construct control arms for single-arm trials provides an option for comparative data. However, non-randomised treatment comparisons have the potential to be biased and cause concern for decision-makers. Using the example of pralsetinib from a RET fusion-positive aNSCLC single-arm trial (NCT03037385), we demonstrate a relative survival benefit when compared to pembrolizumab monotherapy and pembrolizumab with chemotherapy RWD cohorts. Quantitative bias analyses show that results for the RWD-trial comparisons are robust to data missingness, potential poorer outcomes in RWD and residual confounding. Overall, the study provides evidence in favour of pralsetinib as a first-line treatment for RET fusion-positive aNSCLC. The quantification of potential bias performed in this study can be used as a template for future studies of this nature.
Keyphrases
- type diabetes
- advanced non small cell lung cancer
- clinical trial
- study protocol
- open label
- electronic health record
- phase iii
- phase ii
- epidermal growth factor receptor
- big data
- double blind
- high resolution
- human health
- risk assessment
- peripheral blood
- adipose tissue
- data analysis
- metabolic syndrome
- decision making
- mass spectrometry
- locally advanced
- weight loss