“Heterogeneity of treatment effect on patients’ long-term outcome according to pathological response type in neoadjuvant RCTs for breast cancer.”
Laura Pala,
Isabella Sala,
Eleonora Pagan,
Tommaso De Pas,
Emma Zattarin,
Chiara Catania,
Emilia Cocorocchio,
Giovanna Rossi,
Daniele Laszlo,
Giovanni Ceresoli,
Jacopo Canzian,
Elena Valenzi,
Vincenzo Bagnardi,
Fabio Conforti
Affiliations
Laura Pala
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Isabella Sala
Department of Statistics and Quantitative Methods, University of Milan-Bicocca, Milan, Italy; Department of Medicine and Surgery, University of Milan-Bicocca, Milan, Italy
Eleonora Pagan
Department of Statistics and Quantitative Methods, University of Milan-Bicocca, Milan, Italy
Tommaso De Pas
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Emma Zattarin
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Chiara Catania
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Emilia Cocorocchio
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Giovanna Rossi
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Daniele Laszlo
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Giovanni Ceresoli
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Jacopo Canzian
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Elena Valenzi
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Vincenzo Bagnardi
Department of Statistics and Quantitative Methods, University of Milan-Bicocca, Milan, Italy
Fabio Conforti
Department of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy; Department of Oncology and Hemato-oncology, University of Milan, Milan, Italy; Corresponding author. Department of Medical Oncology, Cliniche Humanitas Gavazzeni, Bergamo, 24125, Italy.
Introduction: To provide evidence explaining the poor association between pCR and patients’ long-term outcome at trial-level in neoadjuvant RCTs for breast cancer (BC), we performed a systematic-review and meta-analysis of all RCTs testing neoadjuvant treatments for early-BC and reporting the hazard ratio of DFS (HRDFS) for the intervention versus control arm stratified by pathological response type (i.e., pCR yes versus no). Methods: The objective was to explore differences of treatment effects on DFS across patients with and without pCR.We calculated the pooled HRDFS in the two strata of pathological response (i.e., pCR yes versus no) using a random-effects model, and assessed the difference between these two estimates using an interaction test. Results: Ten RCTs and 8496 patients were included in the analysis.Patients obtaining pCR in the intervention-arm had a higher, although not statistically significant, risk of DFS-event as compared with patients obtaining pCR in the control-arm: the pooled HRDFS for the experimental versus control arm was 1.23 (95%CI, 0.91–1.65). On the opposite, the risk of DFS-event was higher for control as compared with the intervention-arm in the stratum of patients without pCR: the pooled HRDFS was 0.86 (95%CI, 0.78–0.95).Treatment effect on DFS was significantly different according to pathological response type (interaction test p: 0.014). Conclusion: We reported new evidence that contributes to explaining the poor surrogacy value of pCR at trial-level in neoadjuvant RCTs for early-BC.