TROPION-Lung01 Study Design and Baseline demographics slide image

TROPION-Lung01 Study Design and Baseline demographics

Baseline demographics and disease characteristics Data cutoff: July 14, 2023 Received 4.8-8.0 mg/kg R-DXd (OVC population; N=60) Daiichi-Sankyo OVC (4.8-8.0 mg/kg) N=60 4.8 mg/kga (n=13) 5.6 mg/kga (n=8) 6.4 mg/kgb (n=24) 8.0 mg/kg (n=15) Age, median years (range) ECOG PS, n (%) 66 (42-82) Ongoing on treatment: n=9 Ongoing on treatment: n=8 Ongoing on treatment: n=13 Ongoing 0 22 (36.7) on treatment: n=3 1 38 (63.3) Platinum-resistant diseasee, n (%) 55 (91.7) Discontinued (n=27) Number of prior systemic regimens, median (range) 4 (1-13) Received prior systemic therapy, n (%) PD (n=14) Clinical progression (n=2) TEAE (n=9) Otherd (n=2) Bevacizumab 41 (68.3) PARP inhibitor 39 (65.0) • Median treatment duration: 18 weeks (range: 3-115) • 12 (20%) patients received treatment for ≥6 months • 3 (5%) patients received treatment for ≥18 months Baseline tumor CDH6 expression H-score, median (range) 125 (0-250) "Enrollment ongoing. "Enrollment completed. "As of October 2022, the patients who were still receiving R-DXd at 8.0 mg/kg were dose-reduced to receive R-DXD 6.4 mg/kg. "Death (n=1) and informed consent withdrawn (n=1). "Defined as tumor progression during or within 6 months after completion of prior platinum therapy. Five patients had tumor progression 6 months after platinum therapy. CDH8, cadherin 8; ECOG PS, Eastern Cooperative Oncology Group performance status; OVC, ovarian cancer; PARP, poly adenosine diphosphate-ribose polymerase; PD, progressive disease; TEAE, treatment-emergent adverse event. 55
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