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find Author "刘定义" 2 results
  • Clinical Obsevation of Gefitinib on Mutational Unknown Non-small Cell Lung Cancer in End Stage

    【摘要】 目的 评估吉非替尼治疗终末期(PS评分≥3分)非小细胞肺癌(NSCLC)的临床效果和生活质量改善情况。 方法 2008年5月-2010年6月共收治终末期NSCLC患者40例,其中19例患者采用吉非替尼治疗(治疗组),21例采用支持治疗+中药治疗(对照组)。 结果 治疗6个月后,治疗组19例患者中,CR 1例,PR 5例,SD 10例,PD 3例。治疗组有效率为31.5%(6/19),临床受益率为84.2%(16/19)。对照组21例中,SD 5例,PD 16例,无CR。对照组有效率为23.8%(5/21),临床受益率为 23.8%(5/21)。两组间有效率和临床受益率比较,差异均有统计学意义(Plt;0.05)。治疗组中位生存期为13.2个月,对照组中位生存期为4.5个月。 结论 吉非替尼可延长NSCLC患者的生存期,改善其生活质量。【Abstract】 Objective To evaluate the curative effect and life improvement of gefitinib on non-small cell lung cancer (NSCLC) which in the end stage. Methods Forty patients with end-stage NSCLC were treated from May 2008 to June 2010. Nineteen patients of them were treated with gefitinib (treatment group), 21 patients were treated with supportive care and traditional Chinese medicine treatment (control group). Results Six months after treatment, there are one patient with CR, five patients with PR, 10 patients with SD and three patients with PD in the treatment group. The effective rate of treatment group was 31.5% (6/19), clinical benefit rate was 84.2% (16/19). There are five patients with SD, 16 patients with PD, and no one with CR in the control group. The effective rate of the control group was 23.8% (5/21), clinical benefit rate was 23.8% (5/21). The differences of effective rate and clinical benefit rate between two groups were statistically significant (Plt;0.05). The median survival period of the treatment group and control group were 13.2 and 4.5 months respectively. Conclusion Gefitinib can extend the lifetime of NSCLC patients and improve their quality of life.

    Release date:2016-09-08 09:50 Export PDF Favorites Scan
  • 肿瘤M2型丙酮酸激酶对肺癌诊断价值的临床研究

    目的 探讨肺癌患者血浆肿瘤M2 型丙酮酸激酶( TU M2-PK) 水平变化对其诊断的临床意义。方法 用酶联免疫吸附试验( ELISA) 分别检测40 例肺癌患者( 肺癌组) 、40 例良性肺部疾病患者( 良性肺部疾病组) 和40 例正常人( 正常对照组) 血浆TU M2-PK 水平, 并与癌胚抗原( CEA)进行比较分析。结果 癌组患者血浆TU M2-PK 和血清CEA 与良性肺部疾病组和正常对照组比较差异有统计学意义( TU M2-PK:18.6 U/mL比9. 6 和8. 5 U/mL; CEA: 12.02 μg/L比2. 4 和2. 6 μg/L;P 均lt;0.05) 。随病程加重, 肺癌患者血浆TU M2-PK 阳性率逐渐升高, 肺癌Ⅲ、Ⅳ 期患者血浆TU M2-PK和血清CEA 阳性率( 78. 1% 与75. 0% ) 明显高于Ⅰ、Ⅱ 期患者( 50. 0% 与50. 0% , P 均lt;0. 05) 。单独检测血浆TUM2-PK 对肺癌的敏感性为72. 5% , 特异性为90. 2% , 联合CEA 检测敏感度为81. 3% , 特异性为93. 4% 。结论 TU M2-PK 对诊断肺癌有较高的临床价值, 联合CEA 检测可提高肺癌的敏感性。

    Release date:2016-08-30 11:56 Export PDF Favorites Scan
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