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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 陳秀熙(Tony Hsiu-Hsi Chen),嚴明芳(Ming-Fang Yen) | |
dc.contributor.author | Wang-yu Su | en |
dc.contributor.author | 蘇旺裕 | zh_TW |
dc.date.accessioned | 2021-06-13T05:51:06Z | - |
dc.date.available | 2007-08-03 | |
dc.date.copyright | 2006-08-03 | |
dc.date.issued | 2006 | |
dc.date.submitted | 2006-07-06 | |
dc.identifier.citation | 一、中文參考文獻
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Head Neck. 2003 Nov;25(11):911-921. (82) Chen TH, Chiu YH, Luh DL, et al. Community-based multiple screening model: design, implementation, and analysis of 42,387 participants.[see comment]. Cancer 100(8):1734-43. 2004 Apr 15. (83) Chiang CP, Lang MJ, Liu BY, et al. Expression of proliferating cell nuclear antigen (PCNA) in oral submucous fibrosis, oral epithelial hyperkeratosis and oral epithelial dysplasia in Taiwan. Oral Oncol. 2000 Jul;36(4):353-359. (84) Shedd DP, Hukill PB, Bahn S, Farraro RH. Further appraisal of in vivo staining properties of oral cancer. Arch Surg. 1967 Jul;95(1):16-22. (85) Chen TH, Chiu YH, Luh DL, et al. Community-based multiple screening model: design, implementation, and analysis of 42,387 participants.[see comment]. Cancer 100(8):1734-43. 2004 Apr 15. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/33997 | - |
dc.description.abstract | [背景]:
依口腔癌之自然病史可知於惡性轉化成臨床症狀期之前,有相當長期無臨床症狀之「口腔黏膜癌前病變」存在;因此可以經由提供更加有效之篩檢工具,及時偵測出來予以適當介入,進而達到降低口腔癌發生率之終極目標。 [研究目的]: 本研究希望藉由甲苯胺藍試劑使口腔黏膜予以染色之輔助,證實能較目視篩檢偵測出更多之口腔病變。並分析利用此方法從事大規模篩檢是否可以偵測出更多之口腔癌前病變,進而降低口腔癌發生率並透過實證資料評估其成本效益。 [研究設計與方法]: 針對參加基隆市「闔家歡複合式篩檢」年齡大於15歲有「吸菸」或「嚼食檳榔」習慣者之民眾,排除先前已曾經被診斷、曾接受過口腔癌或癌前病變治療、拒絕/無法配合染劑漱口者。曾對甲苯胺藍試劑過敏與患有蠶豆症的個案亦拒絕其加入本研究。經由隨機化分配成兩組-「實驗組」經甲苯胺藍試劑漱口後由專業口腔外科醫師以目視篩檢口腔黏膜;「控制組」只以顏色、氣味相同之「安慰劑」染料漱口後,由不知隨機化分配組別之相同專業口腔外科醫師以目視篩檢口腔黏膜。兩組個案若篩檢結果為陽性則轉介至醫學中心接受複檢,以獲得確定診斷與安排口腔黏膜切片,得到病理組織報告。追蹤個案存活狀況及口腔癌發生至2004/12/31。 [研究結果]: 本研究共計8,101個案同意參與,經扣除資料不全及重覆篩檢者,共計剩餘7,975個案納入分析;實驗組共4,080人(佔51.16%),對照組共3,895人(佔48.84%),兩組於年齡分佈相當。篩檢陽性個案共有711例(8.9%),其中口腔黏膜癌前病變於實驗組共187 例(陽性偵測率4.58%),對照組共170 例(陽性偵測率4.36%);兩組於口腔黏膜癌前病變之偵測率無統計上之差異(p值=0.64)。進一步分析發現實驗組(41/320, 偵測率12.81%)可比對照組(22/293, 偵測率7.51%)偵測更高比例之口腔黏膜下纖維化(p值=0.03)。對照組/實驗組之惡性轉移相對危險性比率為3.25(95%信賴區間為0.34~31.23)。實驗組比對照組口腔癌之發生率比率為0.80(95%信賴區間0.25~2.64)。以「甲苯胺藍試劑」輔助篩檢口腔黏膜癌前病變可以有效降低20%之口腔癌發生率。依隨機模式估計可得口腔黏膜下纖維化、均質性白斑及紅斑的發生率以均質性白斑約每千人一例最高。由均質性白斑進展至非均質性白斑平均約8.3年,由非均質性白斑進展至臨床症狀前期口腔癌平均約9.7年,由口腔黏膜下纖維化進展至臨床症狀前期口腔癌平均約21.5年,由臨床症狀前期口腔癌進展至臨床症狀期口腔癌平均約2個月。從本研究篩檢所得「口腔癌前病變」結果與電腦模擬估計追蹤十年後「口腔癌」發生個案數分別為實驗組10.67位與對照組16.04位,可推得若欲多減少一位口腔癌個案發生,需要多花費新台幣201,015元;每多拯救一個人年,平均需多支出新台幣8,740元。 [結論]: 本研究為首篇利用甲苯胺藍試劑篩檢口腔黏膜癌前病變之隨機試驗。雖然實驗組與對照組在整體在口腔黏膜癌前病變之偵測幾乎無差異,但實驗組比對照組有更高之口腔病變陽性偵測率與可偵測更高比例之口腔黏膜下纖維化。透過成本效益評估,此方法為符合成本效益之大規模篩檢輔助工具。 | zh_TW |
dc.description.abstract | [Background]
Oral squamous cell carcinoma is now the seventh highest type of malignancy in Taiwan. Incidence of oral cancer has continued to increase parallel to the consumption of betel quid since 1980s and with a similar but lesser extent of the consumption of tobacco. Long preclinical detectable phase in oral permalignant lesions (OPL), including oral submucous fibrosis, homogenous leukoplakia, non-homogenous leukoplakia, and erythroplakia, almost preceded the advent of clinical manifest oral cancer. Consequently, with proper screening, these OPLs could be detected early and proper intervention given, hence in hope of reducing incidence of oral cancer. [Study Purpose] (1) To assess whether oral screening with visual inspection with a supplement of Toulidine blue vital dye staining targeting at high risk group (betel quid chewing or smoking) can detect more oral premalignant lesions (2) To quantify the disease natural history for oral cancer and performed a simulation for the cost-effectiveness analysis [Designs and Methods] A community-based randomized controlled trial was designed and conducted in Keelung City in northern Taiwan during 1999. Subjects aged no less than 15 years old with habit of smoking or betel quids chewing were enrolled and randomly assigned into two arms. The experiment group was screened with Toluidine blue dye oral gargling following by visual inspection by experienced oral surgeons. The control group had only placebo dye gargling following by visual inspection by the same blinded oral surgeons. If suspicious oral lesions were identified, referral to tertiary referral medical center for clinical diagnosis and biopsy was arranged. The pathologic report was used as the gold standard for definite diagnosis. Linkage to death registry databank until December 31, 2004 was made to acquire data on occurrence of oral cancer, status of survival and cause of death. Analysis was done on an intention to treat basis. [Results] Of the 8,101 eligible participants recruited in this study, one hundred and twenty-six participants were excluded in the analysis owing to incomplete data collection. A total of 4,080 (51.16%) individuals were included in the experiment group, and 3,895 (48.84%) individuals in the control group. Three hundred and eighty-nine subjects (9.53%) in the experiment group yielded positive screening result while 322 subjects (8.27%) in the control group. After excluding false positive subjects, the positive OPL detection rate was not statistical significant (p=0.64) between the experiment group (4.58%, 187/4,080) and the control group (4.36%, 170/3,895). In subgroup analysis, the detection rate ratio of submucous fibrosis was 1.81 (95%CI 1.05~3.12) between the experiment (41/4,080, 1%) and the control (22/389, 0.56%) group. The relative malignant transformation rate or OPL was 1.29×10-3 in the experiment group and 4.20×10-3 in the control group. The ratio between two groups was 3.25 (95%CI 0.34~31.23) which mean the experiment group tended to detect OPL with higher malignant transformation potential. As for the occurrence oral cancer, it was 11.3×10-5 in the experiment group and 18.45×10-5 in the control group. [Conclusions] The current study is the first one to demonstrate that under the aid of Toluidine blue dye vital staining, mass screening for the high risk subjects could not detect statistically significantly more OPL than screening with visual inspection. The experiment group (41/4,080, 1%) tended to has higher detection rate on oral submucous fibrosis than the control group (22/3,895, 0.56%, p=0.03). In terms of economics, it was a convenient, safe and cost-effective adjunct in mass screening for oral premalignant lesions. Further research with larger cohort or longer follow-up period should be considered to delineate the results more in depth. | en |
dc.description.provenance | Made available in DSpace on 2021-06-13T05:51:06Z (GMT). No. of bitstreams: 1 ntu-95-P93846002-1.pdf: 895950 bytes, checksum: c030eb1d95fd4b4fc1c01dd4c0667387 (MD5) Previous issue date: 2006 | en |
dc.description.tableofcontents | 誌 謝 1
中文摘要 3 Abstract 6 目錄 9 圖表目錄 13 第一章、導論 (Introduction) 16 第一節 研究背景-臺灣地區口腔癌現況 16 第二節 口腔癌前病變之危險因數與口腔癌之關聯性 17 第三節 研究動機與假說 18 第二章、文獻回顧 (Literature Review) 22 第一節 口腔黏膜癌前病變與口腔癌 22 第二節 口腔黏膜癌前病變篩檢方式概論 23 第三節 甲苯胺藍試劑簡介與其作用機制 25 第四節 甲苯胺藍試劑應用於口腔黏膜病變篩檢之文獻回顧 26 第五節 甲苯胺藍試劑活體使用之安全性 28 第六節 甲苯胺藍試劑之活體使用之禁忌 28 第三章、研究設計與方法 (Study Designs & Methods) 31 第一節 研究設計架構與隨機化 31 第二節 研究對象、包含與排除之標準 33 第三節 執行期間及樣本 33 第四節 資料收集 (Data collection) 34 第五節 口腔黏膜病變篩檢前標準化訓練 34 第六節 甲苯胺藍試劑OraScan®之口腔黏膜使用標準流程 35 第七節 資料分析與統計 (Statistical Analysis) 35 第四章、研究結果 (Results) 39 第一節 所有參與實驗個案之基本人口學資料分析 39 第二節 實驗組與對照組基本人口學資料分析 40 第三節 口腔黏膜癌前病變篩檢結果分析 41 第四節 篩檢陽性結果個案依「臨床診斷」之資料分析 43 第五節 實驗組與對照組陽性篩檢結果個案依「口腔黏膜異常部位」之資料分佈 44 第六節 篩檢陽性結果個案「病理切片結果」之資料分佈 46 第七節 口腔黏膜癌前病變之惡性轉移速率 47 第八節 實驗組與對照組之口腔鱗狀細胞癌發生率 48 第九節 口腔癌與癌前病變疾病自然史電腦隨機模擬結果 49 第十節 以甲苯胺藍試劑輔助目視篩檢口腔癌前病變臨床隨機實驗之成本效益評估 50 第五章、討論 (Discussion) 71 第一節、口腔癌前病變偵測率 71 第二節、口腔癌前病變惡性轉移速率 72 第三節、 自然病史隨機模式 72 第四節、 研究限制與建議 74 第六章、結論 (Conclusion) 75 第七章、附錄 (Appendix) 76 第八章、期刊投稿文章 81 Community-Based Screening for Oral Premalignant Lesions using Toluidine Blue dye staining-A Randomized Controlled Trial 81 Natural History for Oral Premalignancy-Oral Cancer and Cost-effectiveness Analysis for Oral Cancer Screening with Toluidine Blue Test as a Supplement to Visual Examination 109 第九章、參考文獻 (References) 128 一、中文參考文獻 128 二、網際網路、網頁參考資料 131 三、英文參考文獻 132 圖表目錄 圖表1.1 民國九十一年臺灣地區十大癌症,按發生率排序 18 圖表1.2 民國九十一年臺灣地區「男性」十大癌症,按發生率排序 19 圖表1.3 民國九十一年臺灣地區「女性」十大癌症,按發生率排序 19 圖表1.4臺灣地區15歲以上居民菸、酒、檳榔平均每人每年消耗之長期趨勢 20 圖表1.5 台灣地區口腔癌年齡標準化發生率之長期趨勢,依性別分,1979-2000年 21 圖表2.1 甲苯胺藍化學結構式(C15H16ClN3S, tolonium chloride) 25 圖表2.2、使用甲苯胺藍試劑做為目視篩檢法「口腔癌與癌前病變」之文獻整理 29 圖表2.2(續)、使用甲苯胺藍試劑做為目視篩檢法「口腔癌與癌前病變」之文獻整理 30 圖表3.1 研究隨機化分配與設計流程圖 32 圖表3.2口腔癌與口腔黏膜癌前病變疾病自然史 36 圖表4.1 口腔黏膜癌前病變篩檢隨機化流程圖與結果 51 圖表4.2 所有參與篩檢個案之基本人口學之資料分佈 52 圖表4.3 所有個案口腔黏膜癌前病變危險因數-抽菸、嚼食檳榔習慣之資料分析 53 圖表4.4 實驗組與對照組基本人口學之資料分析 53 圖表4.5 篩檢陽性個案轉介與接受病理切片狀況分佈 54 圖表4.6所有篩檢陽性結果個案依「臨床診斷」之資料分佈 55 圖表4.7實驗組與對照組陽性篩檢結果個案依「臨床診斷」之資料分佈 56 圖表4.8 實驗組與對照組「口腔黏膜癌前病變」篩檢陽性個案依臨床診斷之分佈 57 圖表4.9實驗組與對照組口腔黏膜癌前病變「盛行率」之比較 58 圖表4.10 各口腔癌前病變之陽性率偵測率與相對陽性偵測率 59 圖表4.11實驗組與對照組陽性篩檢結果個案依「口腔黏膜異常部位」之資料分佈 60 圖表4.12實驗組與對照組陽性篩檢個案依口腔黏膜異常部位之「陽性偵測率」分析 61 圖表4.13實驗組與對照組依各解剖部位之口腔黏膜癌前病變盛行率比較 62 圖表4.14所有篩檢陽性結果個案「病理切片結果」之資料分佈 63 圖表4.15實驗組與對照組陽性篩檢結果個案依「病理切片報告」之資料分佈 64 圖表4.16實驗組與對照組陽性篩檢結果個案依「病理切片報告分類」之資料分佈 65 圖表4.17口腔黏膜癌前病變之惡性轉移速率 66 圖表4.18 實驗組與對照組之口腔鱗狀細胞癌發生率 67 圖表4.19口腔癌與口腔黏膜癌前病變疾病自然史 68 圖表4.20 以馬可夫模型電腦估計口腔癌與癌前病變疾病自然史 68 圖表4.21 利用馬可夫模式估計口腔癌自然病史之內部驗證結果 69 圖表4.22以甲苯胺藍試劑輔助目視篩檢口腔癌預估追蹤十年之成本效益評估 70 附圖表1 口腔黏膜篩檢記錄表格 76 附圖表2 民國九十一年臺灣地區十大癌症,按死亡率排序 77 附圖表3 民國九十一年臺灣地區「男性」十大癌症,按死亡率排序 78 附圖表4 民國九十一年臺灣地區「女性」十大癌症,按死亡率排序 79 附圖表5 民國九十一年臺灣地區「口腔癌」概況 80 | |
dc.language.iso | zh-TW | |
dc.title | 以甲苯胺藍試劑篩檢口腔癌前病變之社區型臨床隨機實驗 | zh_TW |
dc.title | Community-Based Screening for Oral Premalignant Lesions using Toluidine Blue dye staining – A Randomized Controlled Trial | en |
dc.type | Thesis | |
dc.date.schoolyear | 94-2 | |
dc.description.degree | 碩士 | |
dc.contributor.advisor-orcid | ,嚴明芳(mfyen@episerv.cph.ntu.edu.tw) | |
dc.contributor.oralexamcommittee | 江俊斌(Cunh-Pin Chiang),柯政郁(Jenq-Yuh Ko),鄭景暉(Jiiang-Huei Jeng) | |
dc.subject.keyword | 甲苯胺藍試劑,臨床隨機試驗,口腔黏膜癌前病變,口腔黏膜下纖維化,均質性白斑,非均質性白斑,紅斑,鱗狀細胞癌,惡性轉移率, | zh_TW |
dc.subject.keyword | Toluidine blue,randomized controlled trail,oral premalignant lesion,oral submucous fibrosis,homogenous leukoplakia,non-homogenous leukoplakia,erythroplakia,squamous cell carcinoma,malignant transformation rate, | en |
dc.relation.page | 141 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2006-07-06 | |
dc.contributor.author-college | 公共衛生學院 | zh_TW |
dc.contributor.author-dept | 預防醫學研究所 | zh_TW |
顯示於系所單位: | 流行病學與預防醫學研究所 |
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