P32: Oncology trial emulation using real-world electronic health record data: Results of the Coalition to Advance Real-World Evidence through Randomized Controlled Trial Emulation (CARE) initiative

Methods

Following feasibility assessments of candidate RCTs in available U.S. data sources, we emulated the KEYNOTE-189 (metastatic NSCLC) trial of first-line pembrolizumab+chemotherapy vs. chemotherapy in two electronic health record datasets (DS1 and DS2) and the PALOMA-2 (advanced breast cancer) trial of first-line palbociclib+letrozole vs. letrozole in DS1. Trial entry criteria were applied, as feasible. Treatment status was based on first-line regimens (using data partner-defined line of therapy algorithms) initiated during a fixed ascertainment period. Inverse probability of treatment weighting was used to control baseline confounding. Cox proportional hazards models were used to estimate the primary outcome(s). RWD-based estimates were assessed for qualitative agreement (same direction/magnitude) with RCT results.

Results

The KEYNOTE-189 emulation real-world progression-free survival (rwPFS) hazard ratio (HR) in DS2 was of similar magnitude to the RCT finding, whereas the DS1 result did not demonstrate qualitative agreement [RCT: HR=0.52 (0.43, 0.64); DS2: HR=0.64 (0.47, 0.84); DS1: HR=0.81 (0.65, 1.00)]. KEYNOTE-189 emulation real-world overall survival estimates differed from the RCT results [RCT: 0.49 (0.38, 0.64), DS2: 0.89 (0.63, 1.29), DS1: 1.18 (0.95, 1.44)]. The PALOMA-2 emulation rwPFS HR also differed from RCT findings [RCT: HR=0.58 (0.46, 0.72); DS1: HR=0.84 (0.61, 1.23)].

Conclusions

Our results highlight that RWD oncology emulation conclusions depend on dataset features (e.g., care setting, therapy uptake, data completeness), treatment modality, and real-world clinical care. Future work should emphasize fit-for-purpose RWD selection and consideration of real-world care patterns to generate robust, interpretable real-world evidence.