Li Yonghong, Li Wei, Liu Yirui, Peng Yi, Tang Jing, Li Xiaobing
The Department of Oncology, The First People's Hospital of Tianmen, Tianmen, Hubei 431700, P.R. China.
Department of Nursing, Hubei Cancer Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430079, P.R. China.
Mol Clin Oncol. 2024 Dec 19;22(2):21. doi: 10.3892/mco.2024.2816. eCollection 2025 Feb.
The aim of the present study was to investigate the efficacy and safety of anlotinib combined with vinorelbine (NVB) as a second-line treatment for elderly patients with advanced squamous cell lung carcinoma (SqCLC). The present retrospective analysis included 48 elderly patients (aged ≥65 years) diagnosed with advanced SqCLC who received anlotinib in combination with NVB as a second-line therapy between January 2021 and December 2023. The primary endpoints assessed were overall survival (OS), progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR) and safety profile. The median PFS and OS for the cohort was found to be 5.0 and 9.5 months, respectively. By contrast, the ORR and DCR were found to be 29.17 and 70.83%. Further subgroup analysis indicated that patients who experienced specific adverse events (AEs), such as hypertension, proteinuria and hand-foot syndrome during treatment, generally had superior efficacy compared with those who did not experience these AEs (mPFS, 6.0 vs. 4.0 months; mOS, 11.0 vs. 8.5 months). In addition, apart from promising efficacy, patients who experienced common AEs also experienced decreased appetite (35.42%), fatigue (29.17%), hypertension (25%) and hand-foot syndrome (27.08%). Grade 3 or higher AEs occurred in <30% of patients, the majority of which was alleviated through corresponding support care. These results suggest that the combination of anlotinib and NVB as second-line therapy for elderly patients with advanced SqCLC demonstrated promising efficacy and a manageable safety profile. Such regimen may be a viable treatment option for this patient population. However, further prospective studies are required to validate these findings and optimize the dosing schedule for improved therapeutic outcomes.
本研究旨在探讨安罗替尼联合长春瑞滨(NVB)作为老年晚期肺鳞癌(SqCLC)患者二线治疗的疗效和安全性。本项回顾性分析纳入了48例年龄≥65岁、诊断为晚期SqCLC且在2021年1月至2023年12月期间接受安罗替尼联合NVB作为二线治疗的老年患者。评估的主要终点为总生存期(OS)、无进展生存期(PFS)、客观缓解率(ORR)、疾病控制率(DCR)和安全性。该队列的中位PFS和OS分别为5.0个月和9.5个月。相比之下,ORR和DCR分别为29.17%和70.83%。进一步的亚组分析表明,在治疗期间出现特定不良事件(AE)(如高血压、蛋白尿和手足综合征)的患者,其疗效通常优于未出现这些AE的患者(中位PFS,6.0个月对4.0个月;中位OS,11.0个月对8.5个月)。此外,除了疗效良好外,出现常见AE的患者还出现了食欲下降(35.42%)、疲劳(29.17%)、高血压(25%)和手足综合征(27.08%)。3级或更高等级的AE发生在不到30%的患者中,其中大多数通过相应的支持治疗得到缓解。这些结果表明,安罗替尼联合NVB作为老年晚期SqCLC患者的二线治疗显示出有前景的疗效和可控的安全性。这种治疗方案可能是该患者群体的一种可行治疗选择。然而,需要进一步的前瞻性研究来验证这些发现并优化给药方案以改善治疗效果。