par De Caluwé, Alex
;Buisseret, Laurence
;Poortmans, Philip;Van Gestel, Dirk
;Salgado, Roberto;Sotiriou, Christos
;Larsimont, Denis
;Paesmans, Marianne
;Ruscas-Craciun, Ligia Ioana
;Stylianos, Drisis;Vandekerckhove, Christophe;Reyal, Fabien;Isabelle, Veys;Eiger, Daniel;Piccart, Martine;Romano, Emanuela;Ignatiadis, Michail 
Référence BMC cancer, 21, 1, page (899)
Publication Publié, 2021-08-01








Référence BMC cancer, 21, 1, page (899)
Publication Publié, 2021-08-01
Article révisé par les pairs
Résumé : | Residual breast cancer after neo-adjuvant chemotherapy (NACT) predicts disease outcome and is a surrogate for survival in aggressive breast cancer (BC) subtypes. Pathological complete response (pCR) rate, however, is lower for luminal B BC in comparison to the triple negative (TNBC) and HER2+ subtypes. The addition of immune checkpoint blockade (ICB) to NACT has the potential to increase pCR rate but is hampered by the lower immunogenicity of luminal B BC. Novel strategies are needed to stimulate the immune response and increase the response rate to ICB in luminal B BC. |