Effectiveness and Safety of Anlotinib Combined with PD-1 Blockades in Patients with Previously Immunotherapy Treated Advanced Non-Small Cell Lung Cancer: A Retrospective Exploratory Study.

IF 5.1 Q1 ONCOLOGY Lung Cancer: Targets and Therapy Pub Date : 2024-03-25 eCollection Date: 2024-01-01 DOI:10.2147/LCTT.S444884
Xue-Jun Dou, Run-Yang Ma, De-Wang Ren, Qiang Liu, Peng Yan
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Abstract

Objective: This study aimed to investigate the effectiveness and tolerability of anlotinib plus PD-1 blockades in patients with previously immunotherapy treated advanced non-small-cell lung cancer (NSCLC).

Methods: A total of 67 patients with previously immunotherapy treated advanced NSCLC who received anlotinib plus PD-1 blockades in clinical practice were screened retrospectively. All the PD-1 blockades used in this study were approved in China and consisted of sintilimab, camrelizumab, tislelizumab and pembrolizumab. Effectiveness and safety of anlotinib plus PD-1 blockades were assessed, and all patients were followed up regularly. Clinical significance between response status to previous immune-related treatment regimens and therapeutic outcomes of anlotinib plus PD-1 blockades was further explored.

Results: The best overall response among the 67 patients suggested that a partial response was observed in 16 patients, stable disease was noted in 41 patients and progressive disease was found in 10 patients, which yielded an objective response rate of 23.9% (95% CI: 14.3-35.9%) and a disease control rate of 85.1% (95% CI: 74.3-92.6%). Prognostic outcomes indicated that the median progression-free survival (PFS) was 6.1 months (95% CI: 2.37-9.83) and the median overall survival (OS) was 16.5 months (95% CI: 10.73-22.27). Exploratory analysis highlighted that patients who were intolerant to previous immune-related regimens (17 patients) might have a superior prognosis (median OS: 22.3 months vs 12.5 months, P=0.024). Additionally, adverse reactions with any grades during anlotinib plus PD-1 blockades administration were observed in 62 patients (92.5%), of which 31 patients (46.3%) had ≥grade 3 adverse reactions. Most common adverse reactions were fatigue, hypertension, diarrhea and hepatotoxicity.

Conclusion: Anlotinib plus PD-1 blockades demonstrated promising effectiveness and tolerable safety in patients with previously immunotherapy treated advanced NSCLC. Those who were intolerant to previous immune-related regimens might benefit significantly from treatment with anlotinib plus PD-1 blockades. This conclusion should be confirmed in future studies.

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安罗替尼联合 PD-1 阻断剂治疗曾接受免疫疗法治疗的晚期非小细胞肺癌患者的有效性和安全性:一项回顾性探索研究
研究目的本研究旨在探讨安罗替尼联合PD-1阻断剂对既往接受过免疫治疗的晚期非小细胞肺癌(NSCLC)患者的有效性和耐受性:回顾性筛选了67名曾接受免疫疗法治疗的晚期NSCLC患者,这些患者在临床实践中接受了安罗替尼加PD-1阻断剂治疗。本研究中使用的PD-1阻断剂均已在中国获批,包括辛替利单抗、坎瑞珠单抗、替舒瑞珠单抗和pembrolizumab。研究评估了安罗替尼联合PD-1阻断剂的有效性和安全性,并对所有患者进行了定期随访。进一步探讨了既往免疫相关治疗方案的应答状态与安罗替尼加PD-1阻断剂治疗结果之间的临床意义:67例患者的最佳总体反应显示,16例患者出现部分反应,41例患者病情稳定,10例患者病情进展,客观反应率为23.9%(95% CI:14.3-35.9%),疾病控制率为85.1%(95% CI:74.3-92.6%)。预后结果显示,中位无进展生存期(PFS)为 6.1 个月(95% CI:2.37-9.83),中位总生存期(OS)为 16.5 个月(95% CI:10.73-22.27)。探索性分析显示,对既往免疫相关疗法不耐受的患者(17 例)预后可能更好(中位 OS:22.3 个月 vs 12.5 个月,P=0.024)。此外,62名患者(92.5%)在服用安罗替尼加PD-1阻断剂期间出现了任何等级的不良反应,其中31名患者(46.3%)出现了≥3级的不良反应。最常见的不良反应是疲劳、高血压、腹泻和肝毒性:结论:安罗替尼联合PD-1阻断剂对既往接受过免疫治疗的晚期NSCLC患者具有良好的疗效和可耐受的安全性。安罗替尼加PD-1受体阻滞剂治疗那些对既往免疫相关方案不耐受的患者可能会明显获益。这一结论应在今后的研究中得到证实。
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CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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