Park Keunchil, Goto Koichi
Samsung Medical Center, Seoul, Korea.
Curr Med Res Opin. 2006 Mar;22(3):561-73. doi: 10.1185/030079906X89847.
Improvements in first-line therapy of advanced non-small-cell lung cancer (NSCLC) have increased the need for effective second-line treatment options. In a Phase II trial of the anticancer drug gefitinib (IRESSA), greater efficacy was observed in Japanese compared with non-Japanese patients. Furthermore, results from a placebo-controlled Phase III trial (IRESSA Survival Evaluation in Lung cancer [ISEL]) showed that treatment with gefitinib was not associated with a statistically significant improvement in survival in either the overall or adenocarcinoma co-primary populations, although there was marked heterogeneity in survival outcomes between patient groups, with patients of Asian origin achieving a significant survival benefit with gefitinib compared with placebo.
To review the benefit:risk profile of gefitinib in Asian patients with advanced NSCLC.
We identified and reviewed 31 reports (each with >or= 25 patients) of clinical experience with gefitinib 250 mg/day in Asia involving a total of > 2000 patients with refractory NSCLC in Japan, China, Korea and Taiwan by searching EMBASE and Medline databases for publications between 1 January 2003 and 1 July 2005.
In the majority of these reports, objective response rates of > 25% and disease control rates of > 60% have been described. Treatment with gefitinib resulted in a median time to progression of > 3 months and a median survival time of > 6 months in most studies. These 31 reports also demonstrated the efficacy of gefitinib in patients with secondary brain metastases, those with poor performance status (PS) and in patients receiving the drug as first-line treatment. Female gender, adenocarcinoma histology, non-smoking history, good PS and the presence of multiple lung metastases are associated with improved responsiveness to gefitinib. Reflecting the results of previous clinical trials, the reports indicate that gefitinib is generally well tolerated by Asian patients. The incidence of interstitial lung disease appears to be higher in Japanese than non-Japanese patients, although the reasons for this are not clear. Recent findings regarding cellular and genetic factors that may underlie the increased responsiveness to gefitinib among Asian patients are discussed.
晚期非小细胞肺癌(NSCLC)一线治疗的改善增加了对有效二线治疗方案的需求。在一项抗癌药物吉非替尼(易瑞沙)的II期试验中,观察到日本患者的疗效优于非日本患者。此外,一项安慰剂对照的III期试验(肺癌中的易瑞沙生存评估[ISEL])结果显示,在总体人群或腺癌共同主要人群中,吉非替尼治疗与生存率的统计学显著改善无关,尽管患者组之间的生存结果存在明显异质性,与安慰剂相比,亚洲裔患者使用吉非替尼可获得显著的生存益处。
回顾吉非替尼在亚洲晚期NSCLC患者中的获益风险情况。
通过检索EMBASE和Medline数据库,查找2003年1月1日至2005年7月1日期间发表的文献,我们识别并回顾了31篇关于亚洲地区每日250mg吉非替尼临床经验的报告(每篇报告至少25例患者),这些报告共涉及日本、中国、韩国和台湾地区2000多名难治性NSCLC患者。
在这些报告中的大多数中,描述了客观缓解率>25%和疾病控制率>60%。在大多数研究中,吉非替尼治疗导致中位疾病进展时间>3个月,中位生存时间>6个月。这31篇报告还证明了吉非替尼在继发性脑转移患者、体能状态(PS)较差的患者以及接受该药物作为一线治疗的患者中的疗效。女性、腺癌组织学类型、无吸烟史、良好的PS以及存在多个肺转移与对吉非替尼的反应性改善相关。反映先前临床试验的结果,这些报告表明亚洲患者对吉非替尼总体耐受性良好。间质性肺病的发生率在日本患者中似乎高于非日本患者,尽管其原因尚不清楚。讨论了关于可能是亚洲患者对吉非替尼反应性增加基础的细胞和遗传因素的最新发现。