肿瘤研究与临床
腫瘤研究與臨床
종류연구여림상
CANCER RESEARCH AND CLINIC
2009年
7期
458-460
,共3页
张怡飞%徐云华%叶翔谮%李子明%顾琳萍%陆舜
張怡飛%徐雲華%葉翔譖%李子明%顧琳萍%陸舜
장이비%서운화%협상참%리자명%고림평%륙순
癌,非小细胞肺%药物疗法%多西紫杉醇
癌,非小細胞肺%藥物療法%多西紫杉醇
암,비소세포폐%약물요법%다서자삼순
Carcinoma,non-small-cell lung%Drug therapy doeetaxel
目的 观察紫杉醇(泰素)耐药的晚期非小细胞肺癌(NSCLC)患者接受多西紫杉醇(泰素帝)二线治疗后的疗效及毒副反应.方法 回顾性分析2005年1月至2008年5月在上海市胸科医院接受多西紫杉醇二线化学治疗的15例NSCLC患者.评价其疗效及不良反应,并随访无疾病进展时间(PFS)及总生存期(OS).结果 15例患者的疾病控制率为66.7%,中位无疾病进展时间为6个月,中位生存期为17.3个月,1年生存率达到63.3%.主要不良反应包括白细胞减少8例(53.3%),胃肠道反应8例(53.3%),呃逆6例(40%),均属可耐受范围.结论 多西紫杉醇二线治疗在紫杉醇耐药的晚期NSCLC患者中显示了良好疗效,且毒副反应可以耐受.
目的 觀察紫杉醇(泰素)耐藥的晚期非小細胞肺癌(NSCLC)患者接受多西紫杉醇(泰素帝)二線治療後的療效及毒副反應.方法 迴顧性分析2005年1月至2008年5月在上海市胸科醫院接受多西紫杉醇二線化學治療的15例NSCLC患者.評價其療效及不良反應,併隨訪無疾病進展時間(PFS)及總生存期(OS).結果 15例患者的疾病控製率為66.7%,中位無疾病進展時間為6箇月,中位生存期為17.3箇月,1年生存率達到63.3%.主要不良反應包括白細胞減少8例(53.3%),胃腸道反應8例(53.3%),呃逆6例(40%),均屬可耐受範圍.結論 多西紫杉醇二線治療在紫杉醇耐藥的晚期NSCLC患者中顯示瞭良好療效,且毒副反應可以耐受.
목적 관찰자삼순(태소)내약적만기비소세포폐암(NSCLC)환자접수다서자삼순(태소제)이선치료후적료효급독부반응.방법 회고성분석2005년1월지2008년5월재상해시흉과의원접수다서자삼순이선화학치료적15례NSCLC환자.평개기료효급불량반응,병수방무질병진전시간(PFS)급총생존기(OS).결과 15례환자적질병공제솔위66.7%,중위무질병진전시간위6개월,중위생존기위17.3개월,1년생존솔체도63.3%.주요불량반응포괄백세포감소8례(53.3%),위장도반응8례(53.3%),애역6례(40%),균속가내수범위.결론 다서자삼순이선치료재자삼순내약적만기NSCLC환자중현시료량호료효,차독부반응가이내수.
Objective To determine the efficacy and toxicity of docetaxel in patients with paclitaxel-resistant advanced non-small cell lung cancer (NSCLC). Methods The clinical data from 15 patients with NSCLC who were admitted in the Shanghai Chest Hospital from January 2005 to May 2008 were retrospectively analyzed. The effects and toxicities of the second-line treatment were assessed. The progression-free survival time(PFS) and overall survival time(OS) were analyzed. Results The disease control rate was 66.7 %, with a progression-free survival time of 6 months, and a overall survival time of 17.3 months. The 1-year survival rate was 63.3 %. The toxic effects were as expected. Conclusion The doeetaxel-based agent is active in patients with paelitaxel-resistant advanced NSCLC.