Efficacy and Safety of Immunotherapy Combined with Anlotinib as FirstLine Treatment in Older NSCLC Patients with PD-L1 Expression<50.

IF 3.5 4区 医学 Q3 ONCOLOGY
Xiangyu Li, Wei Wang, Chunhua Xu, Qi Yuan
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引用次数: 0

Abstract

Background: Non-small cell lung cancer (NSCLC) predominantly affects older adults; these patients have significant comorbidities, making them unsuitable for chemotherapy. This study aimed to evaluate the efficacy and safety of immune checkpoint inhibitor (ICI) along with anlotinib combination therapy as a first-line treatment in older NSCLC patients with programmed death ligand-1(PD-L1) expression<50%.

Methods: We conducted a retrospective observational study including 73 patients with advanced NSCLC treated at Nanjing Brain Hospital. All patients were aged 75 years or older and received first-line systemic therapy with a combination of PD-1 inhibitors and anlotinib. Clinical data were obtained from electronic medical records and analyzed through Kaplan-Meier estimates and Cox proportional hazards models to assess progression-free survival (PFS), overall survival (OS), and the influence of different variables.

Results: The patients had a median age of 80 years. The median PFS was 9.8 months (95% CI: 7.9-11.7), and the median OS was 19.5 months (95% CI: 17.3-21.7). PD-L1 tumor proportion score (TPS) <1% (χ2=10.263, P=0.001) and absence of treatment-induced hypertension (χ2=12.804, P<0.001) were identified as independent risk factors for poor PFS. Advanced disease stage (χ2=11.900, P=0.001), PD-L1 TPS <1% (χ2=6.643, P=0.010), and having two or more chronic comorbidities (χ2=9.011, P=0.003) were independent risk factors for poor OS. Treatment-related hypertension was observed in 25% of patients and was associated with better PFS.

Conclusion: ICI-anlotinib combination therapy showed promising efficacy and an acceptable safety profile in older NSCLC patients. Future studies involving larger populations are necessary to validate these findings and determine the potential of PD-L1 levels as a biomarker for treatment stratification.

免疫疗法联合安洛替尼作为一线治疗PD-L1表达<50的老年NSCLC患者的疗效和安全性
背景:非小细胞肺癌(NSCLC)主要影响老年人;这些患者有明显的合并症,使他们不适合化疗。本研究旨在评估免疫检查点抑制剂(ICI)联合安洛替尼联合治疗作为程序性死亡配体-1(PD-L1)表达<50%的老年NSCLC患者一线治疗的疗效和安全性。方法:我们对在南京脑科医院治疗的73例晚期非小细胞肺癌患者进行回顾性观察研究。所有患者年龄均在75岁或以上,接受了PD-1抑制剂和anlotinib联合的一线全身治疗。从电子病历中获取临床数据,通过Kaplan-Meier估计和Cox比例风险模型进行分析,评估无进展生存期(PFS)、总生存期(OS)以及不同变量的影响。结果:患者中位年龄80岁。中位PFS为9.8个月(95% CI: 7.9-11.7),中位OS为19.5个月(95% CI: 17.3-21.7)。结论:ci -anlotinib联合治疗在老年NSCLC患者中具有良好的疗效和可接受的安全性。为了验证这些发现,并确定PD-L1水平作为治疗分层的生物标志物的潜力,未来的研究需要涉及更大的人群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current cancer drug targets
Current cancer drug targets 医学-肿瘤学
CiteScore
5.40
自引率
0.00%
发文量
105
审稿时长
1 months
期刊介绍: Current Cancer Drug Targets aims to cover all the latest and outstanding developments on the medicinal chemistry, pharmacology, molecular biology, genomics and biochemistry of contemporary molecular drug targets involved in cancer, e.g. disease specific proteins, receptors, enzymes and genes. Current Cancer Drug Targets publishes original research articles, letters, reviews / mini-reviews, drug clinical trial studies and guest edited thematic issues written by leaders in the field covering a range of current topics on drug targets involved in cancer. As the discovery, identification, characterization and validation of novel human drug targets for anti-cancer drug discovery continues to grow; this journal has become essential reading for all pharmaceutical scientists involved in drug discovery and development.
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