Outcome-specific differences between randomized trials and real-world studies of CDK4/6 inhibitors in hormone receptor-positive, HER2-negative advanced breast cancer: a meta-epidemiological analysis
DOI: https://doi.org/10.1186/s12885-026-17197-3
Manuscript snapshot: 9 October 2026 · Publisher status should be verified at DOI. No claim is made that this copy is the final published version.
Abstract
Background. Real-world evidence is increasingly interpreted alongside randomized clinical trial evidence in oncology, but reported outcomes may differ because of variation in patient selection, treatment composition, follow-up, ascertainment, documentation, and reporting. We examined whether outcomes differed between randomized trials and real-world studies of CDK4/6 inhibitors.
Methods. We searched PubMed, Embase, Cochrane CENTRAL, and Web of Science through December 2025 for phase 2/3 randomized trials and real-world cohort, registry, or postmarketing studies of CDK4/6 inhibitors plus endocrine therapy for first- or second-line treatment of hormone receptor-positive, HER2-negative advanced or metastatic breast cancer. Arm proportions were pooled separately using logit-transformed random-effects models, and between-source differences were assessed using mixed-effects meta-regression.
Results. Eighty-six studies were included: 31 randomized trials (40 arms; 7464 patients) and 55 real-world studies (101 cohorts; 30 858 patients). Real-world cohorts included older patients and greater first-line and palbociclib use. After adjustment, objective response rate was higher in real-world cohorts than in trial arms (51.8% vs 36.6%; P=.031). Laboratory-based adverse events did not differ significantly, whereas symptom-based adverse events were consistently lower in real-world cohorts. Adverse event-related discontinuation was similar (10.6% vs 8.6%; P=.523), whereas dose adjustment was higher in real-world cohorts (50.8% vs 33.4%; P=.016).
Conclusions. Reported single-arm outcomes differed between randomized trials and real-world studies, with the largest differences observed for response and symptom-based adverse-event outcomes. These estimates should be interpreted according to endpoint definition, denominator construction, ascertainment, and reporting.
Publisher reference
The journal associated with this manuscript is BMC Cancer, published by Springer Nature. For official citation details and the version of record, use the DOI link above.