par Modi, Shanu;Jacot, William;Yamashita, Toshinari;Sohn, Joohyuk;Vidal, María Jesus M.;Tokunaga, Eriko;Tsurutani, Junji;Ueno, Naoto T;Prat, Aleix;Chae, Yee Soo;Lee, Keun Seok;Niikura, Naoki;Park, Yeon Hee;Xu, Binghe;Wang, Xiaojia;Gil-Gil, Miguel;Li, Wei;Pierga, Jean Yves Ves J.Y.;Im, Seock–Ah –A;Moore, Halle C F;Rugo, Hope H.S.;Yerushalmi, Rinat;Zagouri, Flora;Gombos, Andrea
;Kim, Sung-Bae;Liu, Qiang;Luo, Ting;Saura, Cristina;Schmid, Peter;Sun, Tao;Gambhire, Dhiraj;Yung, Lotus;Wang, Yibin;Singh, Jasmeet;Vitazka, Patrik;Meinhardt, Gerold;Harbeck, Nadia;Cameron, David A
Référence The New England journal of medicine, 387, 1, page (9-20)
Publication Publié, 2022-07

Référence The New England journal of medicine, 387, 1, page (9-20)
Publication Publié, 2022-07
Article révisé par les pairs
Résumé : | BACKGROUND Among breast cancers without human epidermal growth factor receptor 2 (HER2) amplification, overexpression, or both, a large proportion express low levels of HER2 that may be targetable. Currently available HER2-directed therapies have been ineffective in patients with these “HER2-low” cancers. METHODS We conducted a phase 3 trial involving patients with HER2-low metastatic breast cancer who had received one or two previous lines of chemotherapy. (Low expression of HER2 was defined as a score of 1+ on immunohistochemical [IHC] analysis or as an IHC score of 2+ and negative results on in situ hybridization.) Patients were randomly assigned in a 2:1 ratio to receive trastuzumab deruxtecan or the physician's choice of chemotherapy. The primary end point was progression-free survival in the hormone receptor-positive cohort. The key secondary end points were progression-free survival among all patients and overall survival in the hormone receptor-positive cohort and among all patients. RESULTS Of 557 patients who underwent randomization, 494 (88.7%) had hormone receptor-positive disease and 63 (11.3%) had hormone receptor-negative disease. In the hormone receptor-positive cohort, the median progression-free survival was 10.1 months in the trastuzumab deruxtecan group and 5.4 months in the physician's choice group (hazard ratio for disease progression or death, 0.51; P<0.001), and overall survival was 23.9 months and 17.5 months, respectively (hazard ratio for death, 0.64; P=0.003). Among all patients, the median progression-free survival was 9.9 months in the trastuzumab deruxtecan group and 5.1 months in the physician's choice group (hazard ratio for disease progression or death, 0.50; P<0.001), and overall survival was 23.4 months and 16.8 months, respectively (hazard ratio for death, 0.64; P=0.001). Adverse events of grade 3 or higher occurred in 52.6% of the patients who received trastuzumab deruxtecan and 67.4% of those who received the physician's choice of chemotherapy. Adjudicated, drug-related interstitial lung disease or pneumonitis occurred in 12.1% of the patients who received trastuzumab deruxtecan; 0.8% had grade 5 events. CONCLUSIONS In this trial involving patients with HER2-low metastatic breast cancer, trastuzumab deruxtecan resulted in significantly longer progression-free and overall survival than the physician's choice of chemotherapy. |