...
首页> 外文期刊>Drugs of today: Medicamentos de actualidad >Gefitinib: current status in the treatment of non-small cell lung cancer.
【24h】

Gefitinib: current status in the treatment of non-small cell lung cancer.

机译:吉非替尼:非小细胞肺癌的治疗现状。

获取原文
获取原文并翻译 | 示例

摘要

Gefitinib (Iressa) is a novel drug approved in 28 countries (as of June 2004), including Japan, the US, Canada and Australia as second- and third-line monotherapy for the treatment of locally advanced or metastatic non-small cell lung cancer refractory to prior chemotherapy. Gefitinib is an orally active, epidermal growth factor receptor (EGFR)-tyrosine kinase (EGFR-TK) reversible inhibitor which blocks EGFR phosphorylation and subsequent signal transduction pathways involved in proliferation, metastasis, angiogenesis and apoptosis inhibition. Recently, mutations in the TK domain of the EGFR have been identified in those patients with refractory non-small cell lung cancer who achieved dramatic tumor responses to gefitinib. Although the role of EGFR-TK mutation status in predicting other clinical benefits with gefitinib, i.e. disease stabilization and symptom improvement, is unclear, these findings, along with increasing knowledge of other potential biomarkers of response, are significant developments towards further optimizing the use of gefitinib. Gefitinib has favorable pharmacokinetic and pharmacodynamic properties and low toxicity. No dosage adjustment is required for patient age, body weight, gender, ethnicity or moderate to severe hepatic impairment due to liver metastases. Several clinical studies on gefitinib as monotherapy have demonstrated clinically significant symptom relief, tumor response and good tolerability after failure of chemotherapy-based treatment in non-small cell lung cancer. These studies led to gefitinib approval in many countries as a new therapeutic option for patients with advanced non-small cell lung cancer that failed prior chemotherapy. In contrast to the clinical benefit imparted by gefitinib as monotherapy in patients previously treated with chemotherapy, gefitinib in combination with standard platinum-based chemotherapy in chemonaive patients did not improve either survival or other clinical endpoints in non-small cell lung cancer. This review provides currently available data from clinical studies on gefitinib as monotherapy or in combination with platinum-containing chemotherapy.
机译:吉非替尼(Iressa)是一种新药,已在28个国家(包括日本,美国,加拿大和澳大利亚)批准作为二线和三线单一疗法用于治疗局部晚期或转移性非小细胞肺癌(截至2004年6月)以前的化疗难治。吉非替尼是一种口服活性,表皮生长因子受体(EGFR)-酪氨酸激酶(EGFR-TK)可逆抑制剂,可阻断EGFR磷酸化及随后涉及增殖,转移,血管生成和凋亡抑制的信号转导途径。最近,在难治性非小细胞肺癌患者中发现了EGFR TK结构域的突变,这些患者对吉非替尼产生了显着的肿瘤反应。尽管尚不清楚EGFR-TK突变状态在预测吉非替尼的其他临床益处(即疾病稳定和症状改善)中的作用,但这些发现以及对其他潜在反应生物标志物的认识的增强,是进一步优化使用吉非替尼的重要进展。吉非替尼。吉非替尼具有良好的药代动力学和药效学性质,且毒性低。对于患者年龄,体重,性别,种族或由于肝转移引起的中度至重度肝功能损害,无需调整剂量。吉非替尼单药治疗的多项临床研究表明,在非小细胞肺癌中,基于化学疗法的治疗失败后,临床上明显的症状缓解,肿瘤反应和良好的耐受性。这些研究导致吉非替尼在许多国家获得批准,作为先前化疗失败的晚期非小细胞肺癌患者的新治疗选择。与吉非替尼单药治疗先前接受化疗的患者产生的临床益处相比,吉非替尼联合标准铂类化疗在放化疗患者中并未改善非小细胞肺癌的生存率或其他临床终点。这篇综述提供了吉非替尼作为单药治疗或与含铂化疗联合使用的临床研究的当前可用数据。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号