Ye Jing-Ren, Chen Pei-Hsing, Chuang Jen-Hao, Lin Mong-Wei, Tsai Tung-Ming, Hsu Hsao-Hsun, Chen Jin-Shing
Division of Thoracic Surgery, Department of Surgery, National Taiwan University Hospital, Taipei, Taiwan.
Division of Thoracic Surgery, Department of Surgery, National Taiwan University Hospital Yun-Lin Branch, Yun-Lin, Taiwan.
Front Surg. 2022 Mar 11;9:816018. doi: 10.3389/fsurg.2022.816018. eCollection 2022.
For patients with epidermal growth factor receptor (EGFR)-mutated lung cancer who undergo surgery, adjuvant tyrosine kinase inhibitor (TKI) therapy other than osimertinib is an alternative option. We aimed to discuss the long-term safety and efficacy of TKI treatment in real-world data.
From January 2011 to May 2020, patients with stage II-III EGFR-mutated adenocarcinoma who underwent cancer resection surgery at a single center were enrolled. The primary endpoint was disease relapse, and the secondary endpoint was overall survival. In total, 30 patients were included in the study. In our study, all patients underwent complete resection using video-assisted thoracoscopic surgery. The patients were divided into a dose interruption (prolonged interval use) group and non-dose adjustment group.
The patients' pathological stages were II-III. The initial EGFR TKIs were mostly gefitinib ( = 25, 83%), and others were erlotinib ( = 3, 10%) and afatinib ( = 2, 6%). The mean disease-free survival (DFS) was 53.3 months. The 2- and 5-year DFS rate was 90.0 and 73.3%, respectively. The median TKI treatment duration in this study was 44.5 months (range, 6-133 months), which was the longest in the literature review. Of these patients, nine had dose interruption. We compared the two groups and found no treatment differences between them. There were no significant side effect potentials between both groups.
To our knowledge, this study provides the longest experience of TKI in patients with resected EGFR mutations and also provided a dose reduction strategy (prolonged medication interval) for patients who had intolerable side effects.
对于接受手术的表皮生长因子受体(EGFR)突变型肺癌患者,除奥希替尼外的辅助酪氨酸激酶抑制剂(TKI)治疗是一种替代选择。我们旨在探讨TKI治疗在真实世界数据中的长期安全性和疗效。
2011年1月至2020年5月,纳入在单一中心接受癌症切除手术的II-III期EGFR突变腺癌患者。主要终点为疾病复发,次要终点为总生存期。本研究共纳入30例患者。在我们的研究中,所有患者均采用电视辅助胸腔镜手术进行了根治性切除。患者分为剂量中断(延长间隔使用)组和非剂量调整组。
患者的病理分期为II-III期。初始EGFR-TKI大多为吉非替尼(n = 25,83%),其他为厄洛替尼(n = 3,10%)和阿法替尼(n = 2,6%)。平均无病生存期(DFS)为53.3个月。2年和5年DFS率分别为90.0%和73.3%。本研究中TKI的中位治疗持续时间为44.5个月(范围6-133个月),这是文献综述中最长的。这些患者中,9例有剂量中断。我们比较了两组,发现两组之间无治疗差异。两组之间均无显著的副作用可能性。
据我们所知,本研究提供了TKI治疗切除的EGFR突变患者最长的经验,也为有不可耐受副作用的患者提供了一种剂量降低策略(延长用药间隔)。