DESTINY-Breast03 Phase 3 Study Results slide image

DESTINY-Breast03 Phase 3 Study Results

Time to First Occurrence of Nausea and Vomiting 10 Daiichi-Sankyo DESTINY-Breast03 Nausea + Censor 1.0 Cumulative Probability 0.9 P<0.0001 0.8 0.7 0.6 0.5 0.4 T-DXd T-DM1 0.3 0.2 Cumulative Probability + 1.0¬ Censor T-DXd Vomiting 0.9- T-DM1 P<0.0001 0.8- 0.7- 0.6- www 0.5 0.4- 0.3- 0.2- படட 0.1 0.1 0.0 0.0 0 90 180 270 360 450 540 630 720 810 900 990 1080 0 90 180 270 360 450 540 630 720 810 900 990 1080 Days Days T-DXd 257 T-DM1 261 71 150 59 100 46 37 27 74 50 39 22 20 9 6 29 15 4 42 1 0 0 T-DXd 257 T-DM1 261 153 133 115 95 202 141 95 66 24 79 55 47 53 29 14 8 3 1 0 34 19 7 3 0 Risk of first event of nausea and vomiting was higher with T-DXd in earlier cycles T-DM1, trastuzumab emtansine; T-DXd, trastuzumab deruxtecan; TEAE, treatment-emergent adverse event. Time to first occurrence of the TEAE was defined as the date of the first occurrence of the TEAE minus the date of first study drug plus 1. Patients that did not experience the TEAE were censored at min (treatment end date + 47 days, new treatment start date, death date, date last known alive) minus first study drug date plus 1. P value was from the unstratified log rank test and was for descriptive purposes only. ASCO 2022 #1000 Oral 30
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