Inoue Akira, Yoshida Kazushi, Morita Satoshi, Imamura Fumio, Seto Takashi, Okamoto Isamu, Nakagawa Kazuhiko, Yamamoto Nobuyuki, Muto Satoshi, Fukuoka Masahiro
Department of Palliative Medicine, Tohoku University School of Medicine, Sendai
Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo.
Jpn J Clin Oncol. 2016 May;46(5):462-7. doi: 10.1093/jjco/hyw014. Epub 2016 Mar 13.
The Japan Guidelines of Lung Cancer Therapy recommend epidermal growth factor receptor-tyrosine kinase inhibitors as a first-line therapy for advanced/recurrent non-small cell lung cancer patients with epidermal growth factor receptor mutation. Although survival periods in recent reports of epidermal growth factor receptor-tyrosine kinase inhibitor treatment have been getting longer, the reasons why are unclear. We investigated the survival, prognostic factors and real-world treatment of non-small cell lung cancer patients with epidermal growth factor receptor mutation in clinical practice.
Non-small cell lung cancer patients (n = 1660) who started first-line treatment from January 2008 to December 2012 were enrolled. Patients were diagnosed with epidermal growth factor receptor mutation-positive advanced/recurrent non-small cell lung cancer by histology or cytology samples. The primary objective was to estimate overall survival. The secondary objectives were to determine prognostic factors, real-world treatment patterns and efficacy of gefitinib treatment. We calculated the treatment exposure rate for each treatment category using the following formula: exposure rate = person-years for the treatment category/total person-years × 100.
The median overall survival was 30.8 months. Sex, age, histology, epidermal growth factor receptor mutation type, clinical stage and performance status affected overall survival. The exposure rates for all epidermal growth factor receptor-tyrosine kinase inhibitors, gefitinib and platinum-doublet chemotherapy were 62.1, 46.4 and 8.5% respectively. Overall 56.1% of patients were administered gefitinib as first-line therapy, and 39.0% were treated with ≥2 epidermal growth factor receptor-tyrosine kinase inhibitor regimens. The median progression-free survival in the first-line gefitinib group was 11.4 months. Factors affecting prognosis were sex, histology, clinical stage and performance status.
Epidermal growth factor receptor-tyrosine kinase inhibitors, especially gefitinib, are major components of the treatment regimens for epidermal growth factor receptor mutation-positive non-small cell lung cancer. Switching and re-challenging with epidermal growth factor receptor-tyrosine kinase inhibitors were also practiced in Japan.
日本肺癌治疗指南推荐表皮生长因子受体酪氨酸激酶抑制剂作为表皮生长因子受体突变的晚期/复发性非小细胞肺癌患者的一线治疗方案。尽管近期表皮生长因子受体酪氨酸激酶抑制剂治疗报告中的生存期越来越长,但其原因尚不清楚。我们在临床实践中调查了表皮生长因子受体突变的非小细胞肺癌患者的生存情况、预后因素及实际治疗情况。
纳入2008年1月至2012年12月开始一线治疗的非小细胞肺癌患者(n = 1660)。通过组织学或细胞学样本诊断为表皮生长因子受体突变阳性的晚期/复发性非小细胞肺癌患者。主要目的是评估总生存期。次要目的是确定预后因素、实际治疗模式及吉非替尼治疗的疗效。我们使用以下公式计算每个治疗类别的治疗暴露率:暴露率=治疗类别对应的人年数/总人年数×100。
中位总生存期为30.8个月。性别、年龄、组织学类型、表皮生长因子受体突变类型、临床分期及体能状态影响总生存期。所有表皮生长因子受体酪氨酸激酶抑制剂、吉非替尼及铂类双联化疗的暴露率分别为62.1%、46.4%及8.5%。总体而言,56.1%的患者接受吉非替尼作为一线治疗,39.0%的患者接受≥2种表皮生长因子受体酪氨酸激酶抑制剂方案治疗。一线吉非替尼组的中位无进展生存期为11.4个月。影响预后的因素为性别、组织学类型、临床分期及体能状态。
表皮生长因子受体酪氨酸激酶抑制剂,尤其是吉非替尼,是表皮生长因子受体突变阳性非小细胞肺癌治疗方案的主要组成部分。在日本也采用了表皮生长因子受体酪氨酸激酶抑制剂的换药和再挑战治疗。