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請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/84675
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor陳秀熙(Hsiu-Hsi Chen),侯信安(Hsin-An Hou)
dc.contributor.authorChia-Hsun Leeen
dc.contributor.author李佳勳zh_TW
dc.date.accessioned2023-03-19T22:20:06Z-
dc.date.copyright2022-10-17
dc.date.issued2022
dc.date.submitted2022-09-28
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Incorporation of long non-coding RNA expression profile in the 2017 ELN risk classification can improve prognostic prediction of acute myeloid leukemia patients. EBioMedicine, 40, 240-250. https://doi.org/10.1016/j.ebiom.2019.01.022 Amadori, S., Suciu, S., Selleslag, D., Aversa, F., Gaidano, G., Musso, M., Annino, L., Venditti, A., Voso, M. T., Mazzone, C., Magro, D., De Fabritiis, P., Muus, P., Alimena, G., Mancini, M., Hagemeijer, A., Paolini, F., Vignetti, M., Fazi, P., . . . Baron, F. (2016). Gemtuzumab Ozogamicin Versus Best Supportive Care in Older Patients With Newly Diagnosed Acute Myeloid Leukemia Unsuitable for Intensive Chemotherapy: Results of the Randomized Phase III EORTC-GIMEMA AML-19 Trial. Journal of Clinical Oncology, 34, 972. https://doi.org/10.1200/JCO.2015.64.0060 Arenaza, A., Diez, R., Esteve, J., Di Nicolantonio, R., Gostkorzewicz, J., Martínez, C., Llinàs, D. M., Martinez-Lopez, J., Montesinos, P., & Moure-Fernández, A. (2019). 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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/84675-
dc.description.abstract急性骨髓性白血病(Acute myeloid leukemia, AML)在各種成人血癌裡是發生率最高的白血病,以癌症整體存活狀況來看,急性骨髓性白血病患者存活率低,其標準治療策略是7+3方案,七天阿糖胞苷(Cytarabine)加上三天蒽環類藥物(Anthracycline)。然而「7+3」方案的密集誘導化療有時會造成患者身體負荷過重,特別在年長或嚴重共病的患者。到目前已有多種臨床試驗採用新型的藥物來進行治療,自2017年至今已有十種藥物獲得美國Food and Drug Administration (FDA),包括Venetoclax及針對FLT3抑制劑, IDH1/2抑制劑等標靶藥物或其他新穎治療藥物運用於臨床試驗中。 大部分的標靶治療價格昂貴且未獲台灣FDA核准或不在台灣全民健康保險範圍內,因此本研究提供治療急性骨髓性白血病患者在透過各項分子檢測及標靶治療上的成本效益分析。基於決策分析建立模型,所建構之馬可夫模型 (Markov Model) 提供量性決策分析,並考慮決策過程中的多項不確定因素,評估相較於「7+3」方案治療,使用標靶治療或者利用危險分層對高風險族群之標靶治療結合中低風險族群之「7+3」方案之精準方案的成本效益分析。效益部分利用新治療和「7+3」方案治療患者所得的生活品質調整後生命年(Quality-adjusted life year, QALY)進行估計;成本部分包括基因檢測、治療及住院等等。 本研究利用臺灣本土參數所建構的成本效益分析得到標靶治療與精準治療策略相較於「7+3」方案治療的增量成本效益比(Incremental cost-effectiveness ratio, ICER) ,亦即當每多增加一單位的生活品質調整生命年時將會分別需要9,696美元及11,334美元,低於2021年3倍的國民人均生產毛額98,361美元,機率性成本效益分析顯示當願付成本超過7500美元時精準策略為最具成本效益的抉擇,當願付成本超過7500美元時,標靶治療為最可能具成本效益之策略。以美國情境進行分析時,65歲男性標靶治療比上「7+3」方案治療的ICER為 65,628美元,金額小於付費意願(Willingness to pay, WTP)閥值98,361 美元,因此標靶治療對急性骨髓性白血病患者來說是一種具有成本效益的選擇。zh_TW
dc.description.abstractAcute myeloid leukemia (AML) is the most common acute adult leukemia and poor survival in the patients new diagnosed with AML. The standard treatment for treating AML is ‘7+3’ regimen, over 4 decades already, which is 7 days of Cytarabine and 3 days of an Anthracycline. However, the intensive induction chemotherapy like ‘7+3’ is sometimes unbearable, especially in elderly patients. Many clinical trials have designed to use novel agents for an alternative treatment. Ten agents received approved by U.S. Food and Drug Administration (FDA) for various indications, including several targeted therapies such as Venetoclax, FLT3 inhibitors and IDH inhibitors, they are available in clinical trials for treating AML patients since 2017. However, in most of targeted therapies are expensive and still not in the coverage of National Health Insurance in Taiwan. This study aimed to provide a cost effectiveness analysis for genetic screening and targeted therapies for treating AML patients. Based on the decision-analytical modelling, our goal is to evaluate the cost effectiveness of using new treatment like targeted therapies with ‘7+3’ standard treatment through the modelling of Markov models for providing quantitative analysis and considering the uncertain factors during the decision making process. We used the empirical results from Taiwanese data for the parameters of Markov decision analysis. Compared with ‘7+3’ standard treatment, the incremental cost-effectiveness ratio (ICER) for personalized strategy and target therapy was $9,696 and $11,334, respectively, for one additional quality-adjusted life year (QALY) gained. Both ICERs were lower than three times of GDP per capita, 98,361. Analysis with the probabilistic approach shows the same results.en
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dc.description.tableofcontents口試委員會審定書 i 誌謝Acknowledgements ii 中文摘要 iii ABSTRACT iv 目錄 v 圖目錄 vii 表目錄 viii 第一章 緒論 1 第二章 文獻探討 3 2.1自然病史及醫療選擇策略 3 2.2 精準治療 8 2.3 標靶治療/新興療法 10 2.4 存活分析及風險函數 12 2.5醫療之成本效益分析(Cost-effectiveness analysis, CEA) 14 第三章 研究方法及材料 23 3.1 資料來源 23 3.2 研究方法與建模 24 第四章 研究結果 35 4.1 模型一 : 三種治療策略之效益分析 35 4.2 模型一:機率性敏感度分析(Probability Sensitivity Analysis, PSA) 36 4.3 模型二 : 傳統治療、標靶/新興療法策略之效益分析 36 4.4 模型二:決策系统敏感度分析(Deterministic Sensitivity Analysis,DSA)與機率性敏感度分析(Probability Sensitivity Analysis, PSA) 37 第五章 討論與結論 45 REFERENCE 48
dc.language.isozh-TW
dc.subject急性骨髓性白血病zh_TW
dc.subject效益分析zh_TW
dc.subjectCost-effectiveness analysisen
dc.subjectAMLen
dc.subjectCEAen
dc.title標靶治療於急性骨髓性白血病成本效益分析zh_TW
dc.titleCost Effectiveness Analysis for Targeted Therapy in Patients with Acute Myeloid Leukemiaen
dc.typeThesis
dc.date.schoolyear110-2
dc.description.degree碩士
dc.contributor.oralexamcommittee陳祈玲(Chi-Ling Chen)
dc.subject.keyword效益分析,急性骨髓性白血病,zh_TW
dc.subject.keywordCost-effectiveness analysis,CEA,AML,en
dc.relation.page52
dc.identifier.doi10.6342/NTU202204123
dc.rights.note同意授權(限校園內公開)
dc.date.accepted2022-09-29
dc.contributor.author-college公共衛生學院zh_TW
dc.contributor.author-dept流行病學與預防醫學研究所zh_TW
dc.date.embargo-lift2022-10-17-
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