par Matikas, Alexios;Naume, Bjorn;Wildiers, Hans;Sonke, Gabe GS;Dieci, Maria Vittoria;Karakatsanis, Andreas;Andersson, Anne;Barnekow, Elin;Kessler, Luisa Edman;Einbeigi, Zakaria;Killander, Fredrika;Linderholm, Barbro B.K.;Schiza, Aglaia;Valachis, Antonis;Nearchou, Andreas;Engebraaten, Olav;Porojnicu, Alina;Soland, Mari Hiorth;Mannsåker, Bård;Raj, Sunil Xavier;Blix, Egil Støre;Nordstrand, Cecilie Soma;Lambertini, Matteo;Vernieri, Claudio;Punie, Kevin;Sotiriou, Christos
;Bergh, Jonas;Villacampa, Guillermo;Zouzos, Athanasios;Hellström, Mats;Hartman, Johan;Foukakis, Theodoros
Référence BMJ open, 15, 8, page (e102626)
Publication Publié, 2025-08
;Bergh, Jonas;Villacampa, Guillermo;Zouzos, Athanasios;Hellström, Mats;Hartman, Johan;Foukakis, TheodorosRéférence BMJ open, 15, 8, page (e102626)
Publication Publié, 2025-08
Article révisé par les pairs
| Résumé : | Neoadjuvant therapy is the standard of care for the treatment of human epidermal growth factor receptor 2 (HER2)-positive breast cancer (BC). Studies on first-generation antibody-drug conjugates, such as trastuzumab emtansine (T-DM1), showed equal or slightly lower efficacy than chemotherapy combined with dual HER2 blockade. Trastuzumab deruxtecan (T-DXd) is a next-generation conjugate approved for the treatment of metastatic HER2-positive and HER2-low BC, with greatly improved efficacy compared to T-DM1. |



