藥品參考
Sacituzumab govitecan
Sacituzumab govitecan is a medicine in the class oncology. It is used for breast cancer.
- 藥物類別: Oncology
- 用途: breast cancer
最後更新 來源: US FDA label
僅供醫療專業人員參考。本頁為簡要摘要，並非醫療建議，亦不能取代官方仿單或臨床判斷。開立處方或調劑前請務必核實。
本頁的臨床內容僅提供英文版。
重點資訊
- 藥物類別
- Oncology
- ATC 代碼
- L01FX06
- 常見劑型
- 粉劑
- 常見規格
- 180 mg
- 已知交互作用
- 2 (禁忌併用: 1 · 嚴重: 1)
- 商品名
- 2
- 國家與市場
- 2
用途
作用方式
Trop-2-directed antibody-drug conjugate. The humanized antibody binds Trop-2-expressing cancer cells and is internalized, releasing SN-38, a topoisomerase I inhibitor. SN-38 prevents re-ligation of single strand breaks, causing DNA damage, apoptosis and cell death.
成人常用劑量（仿單摘要）
Triple-negative breast cancer or HR-positive/HER2-negative breast cancer: 10 mg/kg IV infusion on Days 1 and 8 of each 21-day cycle, as a single agent or with pembrolizumab; continue until disease progression or unacceptable toxicity; do not exceed 10 mg/kg
懷孕與哺乳
- 懷孕
- Unsafe Can cause birth defects or embryo-fetal death: it contains SN-38, a genotoxic drug that targets dividing cells. No human or animal reproduction data. Check pregnancy status; use effective contraception during treatment and for 6 months after (men: 3 months).
- 哺乳
- Unsafe No human milk data. The antibody part is large and poorly absorbed, but the SN-38 payload may enter milk. US label: do not breastfeed during treatment and for 1 month after the last dose.
已通報的副作用
- Decreased leukocyte count
- Decreased neutrophil count
- Decreased hemoglobin
- Nausea
- Diarrhea
- Fatigue
黑框警語
- Can cause severe, life-threatening or fatal neutropenia. Withhold for ANC below 1500/mm3 or neutropenic fever; monitor blood counts; give primary G-CSF prophylaxis to patients at increased risk of febrile neutropenia; treat febrile neutropenia with anti-infectives without delay. Can cause severe diarrhea: monitor, give fluids and electrolytes, evaluate for infection and start loperamide; if severe, withhold until ≤ Grade 1 and reduce subsequent doses.
禁忌症
- Severe hypersensitivity reaction to TRODELVY.
哪些人需要特別留意
- Neutropenia occurred in 64% of patients (Grade 3-4 in 48%); monitor ANC and give G-CSF prophylaxis to patients at increased risk.
- Severe diarrhea; evaluate for infection and start loperamide; fluid and electrolyte replacement.
- Serious hypersensitivity and infusion-related reactions including anaphylaxis; premedicate and observe for at least 30 minutes after infusion.
請告知藥師或醫師您是否懷孕或哺乳、是否患有腎臟或肝臟疾病、是否有過敏，以及您正在使用的所有其他藥物或保健品。
重要交互作用 (2)
- Irinotecan + Sacituzumab govitecan Contraindicated
- Sacituzumab govitecan + Siponimod Major
Pro+ 會員專屬
解鎖完整頁面
建立帳號並開始 Pro+ 試用，即可開啟 Sacituzumab govitecan 的完整藥品專論：劑量、懷孕與哺乳、副作用、警示及所有交互作用。
- Dosing by age, kidney and liver function, and further dose lines
- Renal and hepatic dose adjustments
- Dosing in older adults
- How to give it
- Pharmacokinetics
- Patient counselling points
- IV preparation and dilution
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同類別的其他藥品
常見問題
What is Sacituzumab govitecan used for?
Sacituzumab govitecan is a medicine in the class oncology. It is used for Breast cancer.
What side effects have been reported with Sacituzumab govitecan?
Decreased leukocyte count, Decreased neutrophil count, Decreased hemoglobin, Nausea, Diarrhea, Fatigue. Serious warning: Can cause severe, life-threatening or fatal neutropenia.
Can Sacituzumab govitecan be taken in pregnancy or while breastfeeding?
Pregnancy: Unsafe. Can cause birth defects or embryo-fetal death: it contains SN-38, a genotoxic drug that targets dividing cells. No human or animal reproduction data. Check pregnancy status; use effective contraception during treatment and for 6 months after (men: 3 months). Breastfeeding: Unsafe. No human milk data. The antibody part is large and poorly absorbed, but the SN-38 payload may enter milk. US label: do not breastfeed during treatment and for 1 month after the last dose.
What does Sacituzumab govitecan interact with?
MediHelp lists 2 known interactions for Sacituzumab govitecan. Contraindicated: 1 · Major: 1. The most serious include Irinotecan, Siponimod.
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