A single-center observational study (retrospective + prospective) evaluating the real-world efficacy and toxicity profile of Trastuzumab Deruxtecan (T-DXd) in adult female patients with HER2-positive metastatic breast cancer treated at KSAMC, Madinah, Saudi Arabia
Includes patient demographics, treatment lines (2nd line or beyond), dosing schedule, response assessment per RECIST 1.1, and adverse event grading per CTCAE v5.0
Study Type
OBSERVATIONAL
Enrollment
25
Dose 5.4 mg/kg IV Frequency Every 3 weeks (Q3W) Route Intravenous infusion Line of Therapy 2nd line (post-adjuvant progression) or 3rd line and beyond (de novo metastatic)
King Salman Bin Abdulaziz Medical City (KSAMC) - Oncology Center
Madinah, Saudi Arabia
Disease Control Rate (DCR)
proportion of patients achieving CR + PR + SD per RECIST 1.1
Time frame: 2 years
PFS
time from treatment initiation to progression or death
Time frame: 2 years
OS
time from treatment initiation to death from any cause
Time frame: 2 years
Toxcicity
Overall rate of drug-related adverse events and serious adverse events (SAEs)
Time frame: 2 years
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