CPS + EG and Neo-Bioscore predict individual outcomes but not trial results after neoadjuvant therapy for early breast cancer.

作者信息Fabio Conforti, Valentina Nekljudova, Johannes Holtschmidt, Isabella Sala, Eleonora Pagan, Christine Solbach, Michael Untch, Carsten Denkert, Vincenzo Bagnardi, Marzia Bendoni, Peter A Fasching, Andreas Schneeweiss, Hans-Joachim Lück, Carmine Valenza, Giuseppe Viale, Tommaso De Pas, Marion van Mackelenbergh, Jens Huober, Volkmar Müller, Theresa Link, Thomas Karn, Mattea Reinisch, Frederik Marmé, Vesna Bjelic-Radisic, Christian Schem, Andreas Hartkopf, Elmar Stickeler, Claus Hanusch, Jens-Uwe Blohmer, Tanja Fehm, Kerstin Rhiem, Richard D Gelber, Sibylle Loibl
PMID42945961
发布时间2026-10-27
DOI10.1016/j.ccell.2026.10.002

摘要

CPS + EG and Neo-Bioscore are prognostic scores estimating the risk of recurrence after neoadjuvant chemotherapy for early breast cancer, but can they predict the long-term outcomes in a clinical trial? In this study, we assessed their surrogacy values at patient level and trial level for long-term outcomes, using data from 8,359 patients across nine neoadjuvant randomized trials conducted by the German Breast Group (GBG) and AGO-B study group. We found that at the patient level, both scores were significantly associated with outcomes, but at the trial level, the associations with distant disease-free survival (DDFS), invasive disease-free survival (iDFS), and overall survival (OS) were weak for both scores (R2 range = 0.03 to 0.24, with wide confidence intervals). Thus, our findings suggest that CPS + EG and Neo-Bioscore are not reliable surrogate endpoints for predicting long-term treatment benefit in neoadjuvant trials but remain valuable for estimating individual patients' residual risk after neoadjuvant treatments and guiding subsequent treatment decisions for early breast cancer patients.