Monnet Isabelle, Audigier-Valette Clarisse, Girard Nicolas, Vergnenègre Alain, Molinier Olivier, Souquet Pierre Jean, Blanchon François, Bonnetain Franck, Taguieva-Pioger Naila, Lamour Corinne, Wislez Marie
Centre Hospitalier Intercommunal de Créteil, Créteil, France.
Centre Hospitalier Sainte Musse, Toulon, France.
Lung Cancer. 2016 Aug;98:84-90. doi: 10.1016/j.lungcan.2016.05.016. Epub 2016 May 26.
Erlotinib, an inhibitor of tyrosine kinase activity of the epidermal growth factor receptor, is effective in non-small cell lung cancer (NSCLC). Data on erlotinib use in squamous NSCLC are limited. This observational study aimed at evaluating the efficacy and safety of second-line erlotinib in patients with stage IIIB/IV squamous NSCLC in a real-life setting.
Patients with predominantly squamous stage IIIB/IV NSCLC, who failed first-line platinum-based therapy, were recruited and followed-up for 12 months. Patients underwent visits each trimester. Data were derived from case report forms, and functional assessment of cancer therapy-lung (FACT-L) questionnaires.
A total of 152 patients were enrolled; the majority were males (90%) and mean age was 67.7 years. All patients had squamous (97%) or predominantly squamous (3%) NSCLC, of stage IIIB (21%) or IV (79%). Median progression free survival (PFS) and overall survival were 3 and 5.8 months, respectively. Disease progression was observed in the majority of the patients, mostly due to progression of primary tumour and/or metastatic sites, and led to death in 91/107 of patients. Of the 107 deaths reported, none were due to erlotinib. FACT-L questionnaires were interpretable up to the first visit and were in line with PFS data, showing a relatively good quality of life up to Month 3 (mean total score=78.8). No new or unexpected safety issues were reported.
The results of this real-life cohort study like those of previous phase III/IV subgroups study analyses indicate that erlotinib is a valuable option for second-line treatment of stage IIIB/IV squamous NSCLC.
厄洛替尼是一种表皮生长因子受体酪氨酸激酶活性抑制剂,对非小细胞肺癌(NSCLC)有效。关于厄洛替尼用于肺鳞癌的资料有限。本观察性研究旨在评估在现实临床环境中,二线使用厄洛替尼治疗ⅢB/Ⅳ期肺鳞癌患者的疗效和安全性。
招募主要为ⅢB/Ⅳ期肺鳞癌且一线铂类治疗失败的患者,并进行为期12个月的随访。患者每三个月就诊一次。数据来源于病例报告表和癌症治疗-肺部功能评估(FACT-L)问卷。
共纳入152例患者;大多数为男性(90%),平均年龄67.7岁。所有患者均为肺鳞癌(97%)或主要为肺鳞癌(3%),ⅢB期(21%)或Ⅳ期(79%)。中位无进展生存期(PFS)和总生存期分别为3个月和5.8个月。大多数患者出现疾病进展,主要是由于原发肿瘤和/或转移部位进展,导致107例患者中的91例死亡。在报告的107例死亡中,无一例归因于厄洛替尼。FACT-L问卷在首次就诊时仍可解读,且与PFS数据相符,显示在第3个月时生活质量相对较好(平均总分=78.8)。未报告新的或意外的安全问题。
这项现实队列研究的结果与之前Ⅲ/Ⅳ期亚组研究分析的结果一样,表明厄洛替尼是ⅢB/Ⅳ期肺鳞癌二线治疗的一个有价值的选择。