The HER2-targeted antibody-drug conjugate (ADC) T-DXd demonstrated efficacy in heavily pretreated HER2-over- and -low expressing ABC. We aimed to assess the activity of T-DXd in HER2-over/low expressing or IHC-0 ABC, to describe the drug mechanisms of action and to identify biomarkers associated to drug response or resistance. DAISY is an open-label phase II trial to assess the efficacy of T-DXd in ABC with extensive biomarkers analysis (1) in 3 cohorts: Cohort 1 (HER2 over-expressing: 3+ on IHC or ISH+), Cohort 2 (HER2 low-expressing: 1+ or 2+/ISH-) and cohort 3 (HER2-IHC 0). The primary endpoint was the confirmed objective response rate (ORR). Secondary endpoints were clinical benefit rate, duration of response (DOR), progression-free (PFS), overall survival (OS) and safety. Here we report clinical activity and safety with a longer follow-up of 38.4 months [95%CI: 35.3-40.9]. 185 women and 1 man were enrolled between 2019 and 2021. Among the safety population (179 pts), median [range] age was 55 [24-82] years, median number of previous metastatic line was 5 [0-17] and 12 pts harbored triple-negative ABC. Median number of cycles was 10 [1-63]. In December 2023, 6 pts were still on-treatment. The table shows T-Dxd activity in the full analysis set population (177 pts). Important to note, PFS rate at 24 months was 31% [95%CI: 20-43] in cohort 1. A total of 173 pts (96.6%) had at least one treatment-related adverse event (TRAE). Eight pts (4.5%) had drug related ILD or pneumonitis (grade (G) 1 in 6 pts, G2 and G5 in 1 pt each), 18 pts discontinued treatment due to TRAEs.Table: 7PTotalCohort 1Cohort 2Cohort 3BOR confirmed n/N [95%CI]86/177 (48.6%) [41.0; 56.2]48/68 (70.6%) [58.3; 81.0]27/72 (37.5%) [26.4; 49.7]11/37 (29.7%) [15.9; 47.0]Median DOR (months) [95%CI]8.5 [6.8; 9.7]9.7 [7.2; 17.9]7.6 [4.4; 9.4]6.8 [2.8; 17.5]Median PFS (months) [95%CI]7.1 [6.6; 8.7]11.1 [8.5; 14.4]6.8 [4.6; 8.5]4.2 [2.0; 5.7]Median OS (months) [95%CI]19.6 [16.1; 22.3]31.2 [22.4; Not Reached]19.3 [11.5; 22.1]12.1 [8.3; 15.0] Open table in a new tab Consistent with previously reported data, T-DXd showed clinically meaningful activity in pts with HER2-overexpressing ABC and antitumour activity in those with HER2-low and non-expressing ABC during extended follow-up. Safety profile was consistent with previous reports. (1) Mosele F and alNat Med 2023
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