藥碼
HER07
藥名
Trastuzumab 440 mg/Vial
英文商品名
化療 HerZUma 事審針 440 mg
中文商品名
赫珠瑪 凍晶注射劑440毫克
螢幕名
化療 HerZUma 事審針 440 mg
劑型
Inj
規格
440 mg/Vial
成分
藥理分類
Anticancer- Monoclonal antibodies
健保碼
KC011162B5
ATC碼
藥品圖片
外觀圖片
適應症
#高警訊藥品

乳癌、胃癌
Breast cancer, Adjuvant: Treatment of HER2-overexpressing node positive or node negative (estrogen receptor/progesterone receptor negative or with 1 high-risk feature) breast cancer
1. As part of a treatment regimen consisting of doxorubicin, cyclophosphamide, and either paclitaxel or docetaxel
2. As part of a treatment regimen with docetaxel and carboplatin
3. As a single agent following multimodality anthracycline-based therapy.
Breast cancer, metastatic:
1. First-line treatment of HER2-overexpressing metastatic breast cancer (in combination with paclitaxel)
2. Single agent treatment of HER2-overexpressing breast cancer in patients who have received 1 or more chemotherapy regimens for metastatic disease.
Gastric cancer, Metastatic: Treatment of HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma (in combination with cisplatin and either capecitabine or 5-fluorouracil) in patients who have not received prior treatment for metastatic disease.
藥理
Antineoplastic Agent: Anti-HER2, Monoclonal Antibody
Trastuzumab is a monoclonal antibody which binds to the extracellular domain of the human epidermal growth factor receptor 2 protein (HER-2); it mediates antibody-dependent cellular cytotoxicity by inhibiting proliferation of cells which overexpress HER-2 protein.
藥動學
Vd: 44 mL/ kg
Elimination Half Life: 5.8 days (range 1 to 32 days)
禁忌症
Patients with known hypersensitivity to trastuzumab or to any of its excipients.
懷孕分類
哺乳分類
Infant risk cannot be ruled out.
副作用
Common
1. Dermatologic: Rash
2. Endocrine metabolic: Weight decreased
3. Gastrointestinal: Diarrhea, Nausea, Stomatitis, Vomiting
4. Hematologic: Anemia, Neutropenia, Thrombocytopenia
5. Immunologic: Infectious disease
6. Neurologic: Headache, Insomnia
7. Respiratory: Cough
8. Other: Fatigue, Fever, Shivering
Serious
1. Cardiovascular: Cardiac dysrhythmia, Heart failure, Left ventricular cardiac dysfunction, Myocardial ischemia
2. Hematologic: Febrile neutropenia, Neutropenia, Thrombocytopenia, Thrombosis
3. Immunologic: Hypersensitivity reaction
4. Renal: Renal failure
5. Respiratory: Dyspnea, Interstitial pneumonia, Pulmonary hypertension, Pulmonary toxicity
6. Other: Infusion reaction, Tumor lysis syndrome
劑量和給藥方法
Breast cancer (adjuvant, HER2+): IV
1. With concurrent paclitaxel or docetaxel or docetaxel/carboplatin:
Initial 4 mg/kg infused over 90 minutes, followed by maintenance 2 mg/kg infused over 30 minutes weekly for total of 12 weeks, followed 1 week later (when concurrent chemotherapy completed) by 6 mg/kg infused over 30 to 90 minutes every 3 weeks for total therapy duration of 52 weeks
2. Following completion of multi-modality anthracycline-based chemotherapy:
Initial 8 mg/kg infused over 90 minutes, followed by maintenance 6 mg/kg infused over 30 to 90 minutes every 3 weeks for total therapy duration of 52 weeks
Breast cancer (metastatic, HER2+): IV
1. Dosage: Initial 4 mg/kg infused over 90 minutes, followed by maintenance 2 mg/kg infused over 30 minutes weekly until disease progression
2. Administration: either as a single agent or in combination with paclitaxel
Gastric cancer (metastatic, HER2+): IV
1. Dosage: Initial 8 mg/kg infused over 90 minutes, followed by maintenance 6 mg/kg infused over 30 to 90 minutes every 3 weeks until disease progression.
2. Administration: In combination with cisplatin and either capecitabine or fluorouracil for 6 cycles followed by trastuzumab monotherapy
小兒調整劑量
The safety and effectiveness of trastuzumab have not been established in pediatric patients.
腎功能調整劑量
There are no dosage adjustments provided in the manufacturer's labeling.
肝功能調整劑量
There are no dosage adjustments provided in the manufacturer's labeling.
安定性
1. Store unopened vials between 2 and 8 degrees C.
2. After reconstitution with supplied bacteriostatic water for injection, solution may be stored in the refrigerator, between 2 and 8 degrees C, for up to 28 days.
3. Solutions prepared with unpreserved sterile water for injection should be used immediately. Discard any unused solution after 28 days; Do not freeze.
注射給藥指引
給藥途徑

僅限靜脈輸注給藥。絕對不可直接以靜脈推注或快速注射方式給藥。

Intravenous (IV) infusion only. Do not administer as an IV push or bolus.
靜脈輸注液

配製稀釋液:注射用無菌蒸餾水。輸注稀釋液:0.9% 生理食鹽水。請注意,不可使用 5% 葡萄糖溶液進行稀釋,因為這會導致蛋白質發生聚集現象。

Reconstitution diluent: Sterile Water for Injection (SWFI). In
每瓶稀釋液體積

每一瓶 440 毫克的藥粉應使用 20 毫升的注射用無菌蒸餾水進行配製,配製後的濃度約為 21 毫克/毫升。

Each 440 mg vial should be reconstituted with 20 mL of Sterile Water for Injection (SWFI) to yield
注射濃度
給藥速率

起始負荷劑量:靜脈輸注時間需達 90 分鐘。後續維持劑量:若病患對起始負荷劑量的耐受性良好,後續輸注時間可縮短至 30 分鐘。

Initial loading dose: Administer over 90 minutes. Subsequent maintenance doses: If the prior dose was well tolerated, the infusion can be administered over 30 minutes.
安定性
1. Store unopened vials between 2 and 8 degrees C.
2. After reconstitution with supplied bacteriostatic water for injection, solution may be stored in the refrigerator, between 2 and 8 degrees C, for up to 28 days.
3. Solutions prepared with unpreserved sterile water for injection should be used immediately. Discard any unused solution after 28 days; Do not freeze.
注意事項

1. 具有潛在的心臟毒性,在治療前及治療期間應定期監測左心室射出分率 (LVEF)。2. 輸注期間需密切監測輸注相關反應,如出現發燒、發冷或其他過敏症狀,應減慢速率或停止輸注。3. 可能導致胚胎胎兒毒性,育齡婦女應採取避孕措施。4. 不可與其他藥物混合或在同一條靜脈管路中併用。

1. Potential for cardiotoxicity; monitor left ventricular ejection fraction (LVEF) before and during treatment. 2. Closely monitor for infusion-related reactions (IRR); slow or stop the infusion if fever, chills, or hypersensitivity symptoms occur. 3. Risk of embryo-fetal toxicity; females of reproductive potential should use effective contraception. 4. Do not mix or co-administer with other drugs in the same intravenous line.
藥袋資訊
臨床用途
標靶治療藥物
主要副作用
發燒、寒顫、腹痛、無力、頭痛、腹瀉、關節肌肉痛等
泡製方法
儲存方式
請置於 2-8℃ 冷藏儲存
注意事項
其他說明
化療藥局 化冰2 | 藥庫 化療
藥品外觀
顏色
形狀
剝痕
標記1
標記2
其他
健保藥價
28518
自費價
32795.7
仿單
資料庫
健保給付規定