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吉非替尼治疗失败后,厄洛替尼用于从不吸烟的亚洲女性肺腺癌患者。

Erlotinib after Gefitinib failure in female never-smoker Asian patients with pulmonary adenocarcinoma.

作者信息

Sim Sung Hoon, Han Sae-Won, Oh Do-Youn, Lee Se-Hoon, Kim Dong-Wan, Im Seock-Ah, Chung Doo Hyun, Kim Tae-You, Lee Jong Seok, Kim Young Whan, Heo Dae Seog, Bang Yung-Jue

机构信息

Department of Internal Medicine, Seoul National University Hospital, Republic of Korea.

出版信息

Lung Cancer. 2009 Aug;65(2):204-7. doi: 10.1016/j.lungcan.2008.11.006. Epub 2008 Dec 24.

Abstract

The activity of erlotinib after gefitinib failure in non-small cell lung cancer patients with all four favorable clinical factors including female, never smoker, Asian, and adenocarcinoma histology for tyrosine kinase inhibitors (TKIs) is not well known. Treatment efficacy of erlotinib (150mg daily) after progression on gefitinib (250mg daily) was analyzed in patients exhibiting the four clinically favorable factors. Sixteen consecutive female, never smoker, Korean (Asian), adenocarcinoma patients who received erlotinib after gefitinib failure were analyzed. The disease control rate for gefitinib was 68.8% (95% CI, 0.44-0.86) while the disease control rate for erlotinib following gefitinib failure was 25.0% (95% CI, 0.10-0.50) comprised of one partial response and three stable disease patients. The median progression free survival was 6.3 months for gefitinib treatment and 1.7 months for erlotinib treatment following gefitinib failure. The efficacy of erlotinib after progression on gefitinib is unsatisfactory in patients with four favorable clinical factors for TKIs. Novel treatment approaches such as the use of irreversible TKIs or anti-cMET agents for those patients are warranted.

摘要

对于具有女性、从不吸烟、亚洲人以及腺癌组织学这四项酪氨酸激酶抑制剂(TKIs)有利临床因素的非小细胞肺癌患者,吉非替尼治疗失败后厄洛替尼的活性尚不明确。对表现出这四项临床有利因素的患者,分析了吉非替尼(每日250mg)进展后厄洛替尼(每日150mg)的治疗疗效。对16例吉非替尼治疗失败后接受厄洛替尼治疗的连续女性、从不吸烟、韩国(亚洲)腺癌患者进行了分析。吉非替尼的疾病控制率为68.8%(95%CI,0.44 - 0.86),而吉非替尼治疗失败后厄洛替尼的疾病控制率为25.0%(95%CI,0.10 - 0.50),包括1例部分缓解和3例病情稳定的患者。吉非替尼治疗的中位无进展生存期为6.3个月,吉非替尼治疗失败后厄洛替尼治疗的中位无进展生存期为1.7个月。对于具有四项TKIs有利临床因素的患者,吉非替尼进展后厄洛替尼的疗效并不理想。对于这些患者,需要采用新的治疗方法,如使用不可逆TKIs或抗cMET药物。

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