Cytarabine

證據等級: L5 | 預測適應症: 9


## 藥師評估報告

Cytarabine 藥師筆記

一句話總結

Cytarabine (Ara-C) 是治療急性白血病的核心化療藥物,TxGNN 預測其對小細胞肺癌及原發性肺淋巴瘤有療效,這些預測有歷史臨床研究支持,但療效有限且非現代標準治療。


快速總覽

項目 內容
藥物名稱 Cytarabine (阿糖胞苷, Ara-C)
DrugBank ID DB00987
台灣商品名 複方製劑中的成分,如 Midostaurin 併用方案
原核准適應症 急性骨髓性白血病 (AML)、慢性淋巴球性白血病 (CLL)、與其他藥物併用
預測新適應症 small cell lung carcinoma、primary pulmonary lymphoma、well-differentiated fetal adenocarcinoma of the lung、pulmonary blastoma、myeloid leukemia、upper aerodigestive tract neoplasm、ganglioneuroblastoma (disease)、vertebral anomalies and variable endocrine and T-cell dysfunction、腹膜後腫瘤
最高預測分數 0.998 (small cell lung carcinoma)
證據等級 L3 (歷史臨床研究,非現代標準)

預測適應症詳細分析

1. small cell lung carcinoma L2 99.78% 主要分析

為什麼這個預測合理?

Cytarabine 的抗腫瘤機轉支持其對多種惡性腫瘤的潛在活性:

  1. 核苷類似物:Cytarabine 是胞嘧啶核苷的類似物,干擾 DNA 合成
  2. S 期特異性:主要作用於 DNA 合成期,對快速分裂的腫瘤細胞有選擇性
  3. 廣譜活性:歷史上曾用於多種惡性腫瘤的探索性治療

臨床試驗

試驗編號階段狀態人數主要發現
NCT03507244PHASE1, PHASE2COMPLETED34Intrathecal-pemetrexed Combined With Concurrent Involved-field Radiotherapy for ...
NCT00863512PHASE3TERMINATED34A Randomized Phase III Trial of Adjuvant Chemotherapy in Patients With Early Sta...
NCT03101579PHASE1COMPLETED13Intrathecal Pemetrexed for Recurrent Leptomeningeal Metastasis From Non-small Ce...

相關文獻

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2. primary pulmonary lymphoma L2 99.78%

臨床試驗(7 項)

試驗編號階段狀態人數主要發現
NCT00345865PHASE2COMPLETED473Autologous Peripheral Blood Stem Cell Transplant for Patients With Lymphoma
NCT01476839PHASE1COMPLETED25Phase I Study of Yttrium-90 Labeled Anti-CD25 (a-Tac) Monoclonal Antibody Plus B...
NCT02356159PHASE1, PHASE2COMPLETED34A Phase I/II Open Label, Dose Escalation Study of Palifermin (Kepivance) in Pers...
NCT00013533EARLY_PHASE1COMPLETED30Pilot Study of Non-Myeloablative, HLA-Matched Allogeneic Stem Cell Transplantati...
NCT00452374PHASE1, PHASE2COMPLETED48A Phase I-II Study of Oxaliplatin, Fludarabine, Cytarabine and Rituximab in Pati...
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3. well-differentiated fetal adenocarcinoma of the lung L5 99.76%
目前尚無針對此適應症的專門臨床研究。此為 TxGNN 模型預測結果,需進一步驗證。
4. pulmonary blastoma L5 99.76%
目前尚無針對此適應症的專門臨床研究。此為 TxGNN 模型預測結果,需進一步驗證。
5. upper aerodigestive tract neoplasm L4 99.49%

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6. ganglioneuroblastoma (disease) L5 99.36%
目前尚無針對此適應症的專門臨床研究。此為 TxGNN 模型預測結果,需進一步驗證。
7. vertebral anomalies and variable endocrine and T-cell dysfunction L5 99.32%
目前尚無針對此適應症的專門臨床研究。此為 TxGNN 模型預測結果,需進一步驗證。
8. retroperitoneal neoplasm L3 99.23%

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9. neuroblastoma L2 99.19%

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台灣上市資訊

Cytarabine 在台灣主要以下列形式使用:

用途 藥品 說明
AML 前導治療 Midostaurin (彌多妥) 併用 FLT3 突變陽性 AML
AML 鞏固治療 高劑量 Ara-C 標準方案
CLL 治療 Venetoclax 併用低劑量 Ara-C 不適合強化化療的患者

安全性考量

主要毒性

毒性類型 表現 管理
骨髓抑制 嚴重嗜中性球低下、血小板低下 監測 CBC,預防性使用 G-CSF
感染 機會性感染風險高 預防性抗生素、抗黴菌藥
神經毒性 高劑量時可能出現小腦症狀 監測神經功能,調整劑量
消化道 黏膜炎、噁心嘔吐 止吐藥、口腔護理
Ara-C 症候群 發燒、肌痛、骨痛、皮疹 類固醇預防

藥物交互作用注意

  • 其他骨髓抑制藥物:毒性疊加
  • Digoxin:可能降低 digoxin 吸收
  • Flucytosine:競爭性拮抗

藥物-疾病注意事項 (DDSI)

資料來源:DDInter 2.0(原文內容請參閱該網站)

肝臟疾病 🟡 Moderate

  • 注意事項:Cytarabine is extensively metabolized by the liver…

腎臟疾病 🟡 Moderate

  • 注意事項:Cytarabine is primarily eliminated by the kidney…

Infections 🟢 Minor

  • 本藥物在此情況下禁用。需定期監測。風險包括:骨髓抑制、感染。

Bone Marrow Failure Disorders 🟢 Minor

  • 風險包括:骨髓抑制、出血、感染。可能有嚴重不良反應。

結論與下一步

預測評估

評估項目 小細胞肺癌 原發性肺淋巴瘤
機轉合理性
臨床證據 L3 (歷史研究) L2 (CNS 淋巴瘤有 RCT)
文獻支持 中等但過時 較強(用於 CNS 淋巴瘤)

臨床意義評估

小細胞肺癌

  • 不建議臨床使用:現代 SCLC 治療已不包含 cytarabine
  • 現代標準:Cisplatin/Carboplatin + Etoposide,免疫治療 (如 atezolizumab)
  • 歷史價值:反映了知識圖譜能捕捉歷史用藥關聯

原發性肺淋巴瘤/CNS 淋巴瘤

  • 有臨床價值:高劑量 Ara-C 是 CNS 淋巴瘤治療的重要成分
  • 現代方案:通常與 MTX、rituximab 併用
  • 注意事項:「原發性肺淋巴瘤」較罕見,治療通常參考全身性淋巴瘤方案

建議

  1. SCLC:不建議使用 cytarabine,應依循現代治療指引
  2. CNS 淋巴瘤:高劑量 cytarabine 仍有其角色,需由血液腫瘤專科評估
  3. 腦膜轉移:鞘內 cytarabine 或 liposomal cytarabine 為可選方案

整體證據等級

L3 (觀察性研究/歷史臨床經驗) - 有文獻支持但非現代標準治療


本筆記僅供研究參考,不構成醫療建議。任何用藥決策應諮詢專業醫療人員。

最後更新:2026-02-11


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引用本報告

如需引用本報告,請使用以下格式:

APA 格式:

TwTxGNN. (2026). Cytarabine老藥新用驗證報告. https://twtxgnn.yao.care/drugs/cytarabine/

BibTeX 格式:

@misc{twtxgnn_cytarabine,
  title = {Cytarabine老藥新用驗證報告},
  author = {TwTxGNN Team},
  year = {2026},
  url = {https://twtxgnn.yao.care/drugs/cytarabine/}
}

免責聲明
本報告僅供學術研究參考,不構成醫療建議。藥物使用請遵循醫師指示,切勿自行調整用藥。任何老藥新用決策需經過完整的臨床驗證與法規審查。

最後審核:2026-02-20 | 審核者:TwTxGNN Research Team

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