伊馬替尼治療晚期及高危胃腸道間質(zhì)瘤的臨床療效與安全性分析
本文選題:胃腸道間質(zhì)腫瘤 + 蛋白激酶抑制劑��; 參考:《中國普通外科雜志》2017年04期
【摘要】:目的:評價伊馬替尼治療晚期、高危胃腸道間質(zhì)瘤(GIST)的臨床療效及安全性。方法:回顧2011年1月—2016年6月期間收治的173例GIST患者資料,其中晚期患者73例,高�;颊�100例,分別比較兩類患者中服用伊馬替尼患者與未服藥患者的預(yù)后情況。結(jié)果:73例晚期患者平均隨訪31(6~66)個月;Cox回歸分析顯示,其中服用伊馬替尼患者總生存期(OS)明顯長于未服用伊馬替尼患者(1年OS:100.0%vs.78.6%,2年OS:93.1%vs.26.1%;HR=0.040,95%CI=0.011~0.152,P=0.000)。100例高�;颊咂骄S訪45(6~73)個月;亞組分析示,其中術(shù)后服用伊馬替尼1年患者較未服藥患者無復(fù)發(fā)生存期(RFS)明顯延長(3年RFS:66.7%vs.38.5%;HR=0.341,95%CI=0.134~0.868,P=0.024),而服用伊馬替尼2年患者較服用伊馬替尼1年患者RFS也明顯提高(1年RFS:100.0%vs.100.0%,2年RFS:100.0%vs.88.9%,3年RFS:91.7%vs.66.7%;HR=0.108,95%CI=0.015~0.778,P=0.027);5例術(shù)后服用3年伊馬替尼患者3年RFS為100.0%。服用伊馬替尼的主要不良反應(yīng)為浮腫、白細胞下降、胃腸道反應(yīng)等,以1~2級為主。結(jié)論:伊馬替尼治療晚期、高危GIST有較好的安全性,能有效提高患者生存率;高�;颊咝g(shù)后建議至少服用3年伊馬替尼,但是否延長服藥年限仍需更多的臨床研究證實。
[Abstract]:Objective: to evaluate the efficacy and safety of imatinib in the treatment of advanced high-risk gastrointestinal stromal tumors (GIST). Methods: the data of 173 patients with GIST from January 2011 to June 2016 were retrospectively reviewed, including 73 patients with advanced stage and 100 patients with high risk. The prognosis of two groups of patients who took imatinib and those who did not take it were compared. Results the Cox regression analysis showed that the overall survival time of 73 patients with advanced stage was significantly longer than that of those who did not (1 year OS: 100.0vs.78.6a, 2 years OS93.1vs.26.1cm HR0.0404095CI0.0110.152P0.0000.000.100 patients with high risk patients followed up for an average of 45673months). The postoperative survival time of patients taking imatinib for 1 year was significantly longer than that of patients who did not take Imatinib (3 years RFS: 66.7vs.38.5vs.38.5vs.38.5vs.38.5vs.38.5vs.38.5vs.38.5V). The number of patients taking imatinib was 0.134 and 0.868P0.0240.The RFS of patients who took imatinib for 2 years was significantly higher than that of patients taking imatinib for one year (RFS100.0vs.100.0vs.10.9 RF2 years), and three years later, RFScell was 91.7vs.66.7HR0.100.108HR0.108I was 0.0150.778P0.027277.There were 5 cases of RFS in the group of patients taking Imatinib (RFS100.0vs.100.0vs.88.9rand RFSmember 91.7vs.66.7HR0.1085). The RFS was 100.0 for 3 years after treatment with imatinib. The main adverse reactions of taking imatinib were edema, leukopenia, gastrointestinal reaction and so on. Conclusion: high risk GIST has good safety in the late stage of imatinib therapy and can effectively improve the survival rate of the patients. It is recommended that the high risk patients should take imatinib for at least 3 years after operation, but more clinical studies are needed to confirm whether to prolong the duration of treatment.
【作者單位】: 貴州醫(yī)科大學(xué)附屬醫(yī)院胃腸外科;四川大學(xué)華西臨床醫(yī)學(xué)院胃腸外科;
【分類號】:R735
【相似文獻】
相關(guān)期刊論文 前10條
1 魏輝;王建祥;;伊馬替尼治療慢性粒細胞白血病的療效與毒副反應(yīng)[J];中國實用內(nèi)科雜志;2007年20期
2 張振龍;趙瑾;孫雪峰;李允;;伊馬替尼治療慢性粒細胞性白血病致嚴重皮膚損害一例[J];華北國防醫(yī)藥;2007年06期
3 周勵;沈志祥;;伊馬替尼治療慢性粒細胞白血病的最新進展[J];中國實用內(nèi)科雜志;2008年12期
4 牛家華;王椿;;伊馬替尼耐藥慢性粒細胞白血病治療進展[J];世界臨床藥物;2008年05期
5 常曉慧;關(guān)懷;向陽;;伊馬替尼對慢性粒細胞白血病患者生育及生殖的影響[J];癌變·畸變·突變;2010年06期
6 孟凡義,鄭維揚,劉曉力,宋蘭林,徐兵,張鈺;伊馬替尼治療慢性粒細胞白血病26例臨床觀察[J];中華血液學(xué)雜志;2004年05期
7 江倩,陳珊珊,江濱,江浩,陸穎,陸道培;伊馬替尼治療慢性粒細胞白血病加速期療效評價[J];中華血液學(xué)雜志;2004年06期
8 陳心傳,劉霆,崔旭;伊馬替尼治療慢性粒細胞白血病出現(xiàn)腦水腫一例[J];中華血液學(xué)雜志;2004年07期
9 秦亞溱,阮國瑞,劉艷榮,李金蘭,付家瑜,王卉,常艷,江濱,江倩,江浩,丘鏡瀅,陳珊珊,陸道培;實時定量RT-PCR監(jiān)測慢性粒細胞白血病患者伊馬替尼治療過程中bcr/abl mRNA水平[J];中華血液學(xué)雜志;2005年01期
10 佟莉貞,趙玉紅;伊馬替尼治療兒童慢性粒細胞白血病二例[J];中華血液學(xué)雜志;2005年01期
相關(guān)會議論文 前10條
1 羅依;譚亞敏;施繼敏;鄭高峰;韓曉燕;朱曉黎;黃河;;伊馬替尼聯(lián)合清髓異基因造血干細胞移植治療進展期慢性粒細胞白血病[A];2009年浙江省血液病學(xué)學(xué)術(shù)年會論文集[C];2009年
2 王愛華;李軍民;沈志祥;陳賽娟;陳竺;;伊馬替尼聯(lián)合白血康治療進展期慢性粒細胞性白血病療效評估[A];中華醫(yī)學(xué)會第八次全國血液學(xué)學(xué)術(shù)會議論文匯編[C];2004年
3 Neil P.Shah;;伊馬替尼失效的機制和對策[A];第九次全國血液學(xué)學(xué)術(shù)會議繼續(xù)醫(yī)學(xué)教育資料匯編[C];2006年
4 孫慧;甘思林;馬杰;;伊馬替尼治療成人慢性粒細胞白血病療效及安全性分析[A];第12屆全國實驗血液學(xué)會議論文摘要[C];2009年
5 羅依;譚亞敏;韓曉雁;朱曉黎;鄭偉燕;謝萬灼;張潔;葉t摻,
本文編號:1876855
本文鏈接:http://sikaile.net/yixuelunwen/zlx/1876855.html