Suppr超能文献

吉非替尼作为脑转移肺腺癌的姑息治疗。

Gefitinib as palliative therapy for lung adenocarcinoma metastatic to the brain.

作者信息

Wu Chi, Li Yun Long, Wang Zhao Meng, Li Zhang, Zhang Tong Xiao, Wei Zhong

机构信息

Department of Respiratory Diseases, Peking Union Medical College Hospital, China.

出版信息

Lung Cancer. 2007 Sep;57(3):359-64. doi: 10.1016/j.lungcan.2007.03.011. Epub 2007 Apr 16.

Abstract

BACKGROUND

Lung cancer is the leading cause of cancer deaths in most countries. In patients with metastases, such as the brain, the 1-year survival is 10% and most of these patients die in 1-3 months. Data from large phase II trials of non-small cell lung cancer (NSCLC) suggested that the histologic subtype of adenocarcinoma may be a prognostic factor for patients treated with gefitinib. To evaluate the efficacy of gefitinib in palliative therapy for advanced patients with adenocarcinoma and brain metastases, we conducted a phase II study.

PATIENTS AND METHODS

Eligible patients had histologically confirmed adenocarcinoma and brain metastases confirmed with radiological studies. All eligible patients had undergone chemotherapy previously. From December 2003 to December 2004, 40 patients received 250mg doses of gefitinib daily. The symptomatic response, survival, and toxicity were recorded.

RESULTS

The overall objective response rate was 32% with a disease control rate of 77%. Altogether, 45% of the patients experienced symptom improvement. The median progression-free survival and overall survival were 9.0 months and 15.0 months, respectively. Gefitinib was well-tolerated, with cutaneous reactions as the most frequent toxicity.

CONCLUSIONS

Our data suggest that gefitinib has promising activity in palliative therapy for patients with advanced lung adenocarcinoma and brain metastasis.

摘要

背景

在大多数国家,肺癌是癌症死亡的主要原因。在有转移的患者中,如脑转移患者,1年生存率为10%,且大多数患者在1 - 3个月内死亡。非小细胞肺癌(NSCLC)大型II期试验的数据表明,腺癌的组织学亚型可能是接受吉非替尼治疗患者的一个预后因素。为了评估吉非替尼在晚期腺癌和脑转移患者姑息治疗中的疗效,我们进行了一项II期研究。

患者与方法

符合条件的患者经组织学确诊为腺癌且经影像学检查确诊有脑转移。所有符合条件的患者此前均接受过化疗。2003年12月至2004年12月,40例患者每日接受250mg剂量的吉非替尼治疗。记录症状缓解情况、生存率和毒性反应。

结果

总体客观缓解率为32%,疾病控制率为77%。共有45%的患者症状得到改善。无进展生存期和总生存期的中位数分别为9.0个月和15.0个月。吉非替尼耐受性良好,皮肤反应是最常见的毒性反应。

结论

我们的数据表明,吉非替尼在晚期肺腺癌和脑转移患者的姑息治疗中具有有前景的活性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验