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纳武利尤单抗联合多西他赛治疗免疫检查点抑制剂进展后的真实世界疗效:正在进行的非干预性 VARGADO 研究结果。

Real-World Efficacy of Nintedanib Plus Docetaxel After Progression on Immune Checkpoint Inhibitors: Results From the Ongoing, Non-interventional VARGADO Study.

机构信息

Department of Pneumology, ELK Berlin, Berlin, Germany.

Department of Internal Medicine IV/V (Hematology/Oncology), University Hospital Giessen, Giessen, Germany.

出版信息

Clin Oncol (R Coll Radiol). 2022 Jul;34(7):459-468. doi: 10.1016/j.clon.2021.12.010. Epub 2022 Jan 7.

Abstract

AIMS

To evaluate the efficacy and safety of nintedanib plus docetaxel in patients with advanced adenocarcinoma non-small cell lung cancer (NSCLC) who progressed after chemotherapy and immune checkpoint inhibitor (ICI) therapy.

MATERIALS AND METHODS

VARGADO (NCT02392455) is an ongoing, prospective, non-interventional, real-world study of nintedanib plus docetaxel after first-line chemotherapy in the routine clinical treatment of patients with locally advanced, metastatic or locally recurrent adenocarcinoma NSCLC. Data were collected during routine visits. We report the results from cohort B (n = 80), who received third-line nintedanib plus docetaxel after first-line chemotherapy and second-line ICI therapy.

RESULTS

The median duration of follow-up was 12.4 months. Median progression-free survival from initiation of third-line nintedanib plus docetaxel was 6.4 months (95% confidence interval 4.8, 7.3); median overall survival was 12.1 months (95% confidence interval 9.4, 13.5). The 1-year overall survival rate after initiation of third-line nintedanib plus docetaxel treatment (primary end point) was 52% (95% confidence interval 38.0%, 64.4%). Among 64 patients with a documented response, the objective response rate was 50% (n = 32; one complete response and 31 partial responses) and the disease control rate was 86% (n = 55). There were no new safety signals or unexpected toxicities. Among all treated patients, 74% (n = 59) experienced drug-related adverse events, most commonly (nintedanib-related/docetaxel-related) diarrhoea (34%/24%), a decreased white blood cell count (11%/19%) and nausea (13%/16%).

CONCLUSIONS

Nintedanib plus docetaxel demonstrated a high response rate and disease stabilisation in the third-line setting after failure of prior chemotherapy and ICI treatment, with a manageable safety profile. These results suggest that nintedanib plus docetaxel represents an efficient treatment option after failure of prior ICIs. The ongoing VARGADO study provides valuable real-world data to inform clinical decision-making regarding treatment sequencing after chemotherapy and ICI failure in patients with adenocarcinoma NSCLC.

摘要

目的

评估尼达尼布联合多西他赛在化疗和免疫检查点抑制剂(ICI)治疗后进展的晚期腺非小细胞肺癌(NSCLC)患者中的疗效和安全性。

材料和方法

VARGADO(NCT02392455)是一项正在进行的、前瞻性的、非干预性的真实世界研究,评估尼达尼布联合多西他赛在一线化疗后常规临床治疗局部晚期、转移性或局部复发性腺 NSCLC 患者中的疗效。数据在常规就诊时收集。我们报告了队列 B(n=80)的结果,这些患者在一线化疗和二线 ICI 治疗后接受了三线尼达尼布联合多西他赛治疗。

结果

中位随访时间为 12.4 个月。从开始三线尼达尼布联合多西他赛治疗到疾病进展的中位无进展生存期为 6.4 个月(95%置信区间 4.8,7.3);中位总生存期为 12.1 个月(95%置信区间 9.4,13.5)。三线尼达尼布联合多西他赛治疗开始后(主要终点)的 1 年总生存率为 52%(95%置信区间 38.0%,64.4%)。在有记录的反应的 64 名患者中,客观缓解率为 50%(n=32;1 例完全缓解和 31 例部分缓解),疾病控制率为 86%(n=55)。无新的安全性信号或意外毒性。在所有接受治疗的患者中,74%(n=59)发生了药物相关不良反应,最常见的是(尼达尼布相关/多西他赛相关)腹泻(34%/24%)、白细胞计数下降(11%/19%)和恶心(13%/16%)。

结论

尼达尼布联合多西他赛在先前化疗和 ICI 治疗失败后三线治疗中显示出高缓解率和疾病稳定,安全性可管理。这些结果表明,尼达尼布联合多西他赛是先前 ICI 治疗失败后的有效治疗选择。正在进行的 VARGADO 研究提供了有价值的真实世界数据,为化疗和 ICI 失败后腺 NSCLC 患者的治疗顺序决策提供信息。

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