期刊文献+

四环素、顺铂、氟美西诺随机对照治疗非小细胞肺癌恶性胸腔积液 被引量:1

Tetracycline, DDP and Flumecinol in treating malignant pleural effusion in NSCLC patients: a randomized study
在线阅读 下载PDF
导出
摘要 目的 通过前瞻性随机对照临床试验,探讨四环素、顺铂、氟美西诺(胞必佳)3种药物治疗非小细胞肺癌(NSCLC)恶性胸腔积液疗效和不良反应。方法 105例经组织学或细胞学确诊的NSCLC恶性胸腔积液患者胸水引流后,随机分为3组,胸腔内分别注入四环素500mg、顺铂100mg或胞必佳600μg,2周后复查胸片评价疗效。结果 105例患者胸腔注药后的总有效率为69.5%;四环素组有效率为73.5%,中位缓解期为7.3个月;顺铂组有效率为66.7%,中位缓解期为5.7个月;氟美西诺组有效率为68.6%,中位缓解期为7.1个月;3组有效率无统计学差异。治疗不良反应有不同程度发热、胸病及胃肠道反应,无骨髓抑制及肝肾损害。结论 四环素、顺铂、氟美西诺是治疗NSCLC恶性胸腔积液的有效药物,有效率相当,不良反应各异。 Objective This prospective randomized study is to evaluate the efficacy and side effect of pleural space perfusion with Tet- racycline,Cisplatin (DDP) and Flumecinol (N-CWS) in treating malignant pleural effusion in non-small cell lung cancer (NSCLC) patients. Method 105 NSCLC patients with malignant pleural effusion were randomized into three groups. group 1: Tetracycline 500mg, group 2:DDP 100mg, group 3: N-CWS 600mg. The three drugs were perfused into thoracic cavity after drainage of the pleu- ral effusion. Efficacy was evaluated two weeks later by chest X-ray examination. Result The overall response rate was 69. 5% and 73. 5% for group 1, 66. 7% for group 2, 68. 6% for group 3 respectively. There is no statistically difference of response rate between the three groups. The medium TTP was 7. 3 months for group 1, 5. 7 months for group 2, 7. 1 months for group 3. The main adverse effects contain different degrees of fever, chest pain, and nausea, vomiting. There is no myelosuppression and damage of liver and kid- ney function. Conclusion Pleural space perfusion with Tetracycline, DDP or N-CWS was effective in treating malignant pleural effu- sion of NSCLC patients. The response rate had no difference statistically whereas the side effects showed some difference in three groups.
出处 《广东药学》 2004年第4期46-49,共4页 Guangdong Pharmaceutical Journal
关键词 恶性胸腔积液 非小细胞肺癌 四环素 顺铂 氟美西诺 Malignant pleural effusion Non-small cell lung cancer (NSCLC) Tetracycline cisplatin (DDP) Flumecinol (NCWS)
  • 相关文献

参考文献6

二级参考文献10

共引文献226

同被引文献8

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部