Kabuto Takafumi, Menju Toshi, Nishikawa Shigeto, Terada Kazuhiro, Yoshizawa Akihiko, Date Hiroshi
Department of Thoracic Surgery, Kyoto University Hospital, Kyoto, Kyoto, Japan.
Department of Thoracic Surgery, Japanese Red Cross Wakayama Medical Center, Wakayama, Wakayama, Japan.
Ann Thorac Cardiovasc Surg. 2025;31(1). doi: 10.5761/atcs.oa.24-00149.
We aimed to elucidate the efficacy of conventional cisplatin-based adjuvant chemotherapy for patients with lung cancers harboring epidermal growth factor receptor (EGFR) mutation.
This retrospective cohort study included 110 patients (EGFR mutation group: n = 51; EGFR wild-type group: n = 59) receiving cisplatin-based adjuvant chemotherapy following complete resection of non-small-cell non-squamous-cell lung cancer (2010-2021). Clinicopathological characteristics, recurrence-free survival (RFS), and overall survival (OS) were investigated.
The pStage distribution was not statistically different. The EGFR mutation group was characterized by more advanced pN, papillary predominance, and presence of micropapillary components, whereas the EGFR wild-type group exhibited more advanced pT and solid predominant patterns. The median RFS was significantly worse in the EGFR mutation group (23.0 vs. 76.1 months, p = 0.017). Nevertheless, the median OS was not significantly different (85.6 months vs. not reached, p = 0.151). Multivariable analysis demonstrated that EGFR mutation and lymphatic invasion were significant risk factors in RFS; however, no independent factors were identified in OS.
Cisplatin-based adjuvant chemotherapy might be less effective in patients with EGFR-mutated lung cancer. The style of progression and histological pattern related with EGFR mutation may be associated with the efficacy of adjuvant chemotherapy and poor RFS.
我们旨在阐明基于顺铂的传统辅助化疗对携带表皮生长因子受体(EGFR)突变的肺癌患者的疗效。
这项回顾性队列研究纳入了110例在非小细胞非鳞状细胞肺癌完全切除术后接受基于顺铂的辅助化疗的患者(EGFR突变组:n = 51;EGFR野生型组:n = 59)(2010 - 2021年)。研究了临床病理特征、无复发生存期(RFS)和总生存期(OS)。
p分期分布无统计学差异。EGFR突变组的特征是pN更晚期、乳头为主型以及存在微乳头成分,而EGFR野生型组表现出更晚期的pT和实体为主型模式。EGFR突变组的中位RFS显著更差(23.0个月对76.1个月,p = 0.017)。然而,中位OS无显著差异(85.6个月对未达到,p = 0.151)。多变量分析表明,EGFR突变和淋巴浸润是RFS的显著危险因素;然而,在OS中未确定独立因素。
基于顺铂的辅助化疗对EGFR突变型肺癌患者可能效果较差。与EGFR突变相关的进展方式和组织学模式可能与辅助化疗的疗效及较差的RFS有关。