Cao Feiyi, Wang Wenjing, Gu Cuiping, Zhou Yao, Jin Ying, Hong Wei
Department of Medical Oncology, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, China.
Department of Medical Oncology, Postgraduate Training Base Alliance of Wenzhou Medical University (Zhejiang Cancer Hospital), Hangzhou, China.
J Thorac Dis. 2024 Oct 31;16(10):6483-6495. doi: 10.21037/jtd-24-940. Epub 2024 Oct 30.
Lung cancer is the leading cause of cancer-related mortality worldwide. S-1, a fluorouracil derivative known for its efficacy and minimal adverse effects in various solid tumors, offers hope for advanced non-small cell lung cancer (NSCLC) patients. This study conducted a retrospective, single-center analysis to investigate the effectiveness and safety of S-1 monotherapy and combination therapy as second-line or subsequent treatment for advanced NSCLC.
A total of 52 patients diagnosed with advanced NSCLC at Zhejiang Cancer Hospital (Hangzhou, China) from January 1, 2018, to August 31, 2023 were included in a retrospective study. Among these patients, 13 received S-1 monotherapy while 39 received S-1 in combination therapy. The study aimed to analyze the short-term efficacy, long-term outcome, prognostic factors, and treatment-related adverse events (AEs).
The objective response rate (ORR) was 28.8%, with a median progression-free survival (PFS) of 2.7 months [95% confidence interval (CI): 2.1-2.8] and a median overall survival (OS) of 9.5 months (95% CI: 6.3-12.6) for the entire cohort. The combination therapy with S-1 was determined to be a significant independent predictor of OS, while treatment line was identified as an independent negative prognostic factor for OS. The most prevalent AE observed was anemia, affecting 12 patients (23.1%). The majority of AEs were classified as grade 1-2, with only 3 patients (5.7%) experiencing grade 3-4 AEs. Further prospective studies are recommended to fully assess the therapeutic value of this treatment approach.
Results indicated that both S-1 monotherapy and combination therapy showed promising efficacy and were well tolerated as second-line or later-line treatments for patients with advanced NSCLC. Further prospective studies are recommended to fully assess the therapeutic value of this treatment approach.
肺癌是全球癌症相关死亡的主要原因。S-1是一种氟尿嘧啶衍生物,因其在各种实体瘤中的疗效和最小的副作用而闻名,为晚期非小细胞肺癌(NSCLC)患者带来了希望。本研究进行了一项回顾性单中心分析,以调查S-1单药治疗和联合治疗作为晚期NSCLC二线或后续治疗的有效性和安全性。
一项回顾性研究纳入了2018年1月1日至2023年8月31日期间在浙江省肿瘤医院(中国杭州)诊断为晚期NSCLC的52例患者。在这些患者中,13例接受S-1单药治疗,39例接受S-1联合治疗。该研究旨在分析短期疗效、长期结局、预后因素和治疗相关不良事件(AE)。
整个队列的客观缓解率(ORR)为28.8%,中位无进展生存期(PFS)为2.7个月[95%置信区间(CI):2.1 - 2.8],中位总生存期(OS)为9.5个月(95% CI:6.3 - 12.6)。S-1联合治疗被确定为OS的显著独立预测因素,而治疗线被确定为OS的独立负面预后因素。观察到的最常见AE是贫血,影响了12例患者(23.1%)。大多数AE被分类为1 - 2级,只有3例患者(5.7%)经历3 - 4级AE。建议进一步进行前瞻性研究以全面评估这种治疗方法的治疗价值。
结果表明,S-1单药治疗和联合治疗均显示出有前景的疗效,并且作为晚期NSCLC患者的二线或后续治疗耐受性良好。建议进一步进行前瞻性研究以全面评估这种治疗方法的治疗价值。