根据化疗免疫疗法治疗的晚期非小细胞肺癌患者中性粒细胞与淋巴细胞比率的基线和早期变化进行风险分层:一项多中心真实世界研究。

IF 4.4 3区 医学 Q2 ONCOLOGY Targeted Oncology Pub Date : 2024-09-01 Epub Date: 2024-07-11 DOI:10.1007/s11523-024-01084-7
Kinnosuke Matsumoto, Yuji Yamamoto, Takayuki Shiroyama, Tomoki Kuge, Masahide Mori, Motohiro Tamiya, Yuhei Kinehara, Akihiro Tamiya, Hidekazu Suzuki, Satoshi Tobita, Kiyonobu Ueno, Toshie Niki, Izumi Nagatomo, Yoshito Takeda, Atsushi Kumanogoh
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引用次数: 0

摘要

背景:化疗免疫疗法是晚期非小细胞肺癌(NSCLC)的标准治疗方法:化学免疫疗法是晚期非小细胞肺癌(NSCLC)的标准治疗方法。然而,有关临床预测因素的数据仍然很少:我们旨在确定接受化疗免疫疗法患者的临床生物标志物:这项多中心、真实世界队列研究纳入了2018年12月至2022年5月期间接受化疗免疫治疗的化疗患者。采用多变量分析确定生存结果与患者背景之间的关联,包括基线中性粒细胞与淋巴细胞比值(NLR)及其动态变化(ΔNLR)。为了进一步研究 NLR 的临床意义,根据 NLR 和 ΔNLR 组合定义的患者外周免疫状态对其进行了分类:研究共纳入 280 名患者,中位随访时间为 30.1 个月。多变量分析显示,年龄大、表现状态差、肿瘤比例评分小于1%、肝转移、基线NLR≥5和ΔNLR≥0与无进展生存期和总生存期(OS)的缩短有显著相关性。外周免疫状态较高的患者(定义为 NLR 结论:NLR ≥ 5 和 ΔNLR ≥ 0 与无进展生存期和总生存期(OS)缩短有明显相关性:我们的研究为化疗免疫疗法疗效的临床预后因素提供了真实的证据。对基线NLR和ΔNLR进行联合评估有助于确定哪些患者有可能从化疗免疫疗法中获得持久的反应。
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Risk Stratification According to Baseline and Early Change in Neutrophil-to-Lymphocyte Ratio in Advanced Non-Small Cell Lung Cancer Treated with Chemoimmunotherapy: A Multicenter Real-World Study.

Background: Chemoimmunotherapy is a standard treatment for advanced non-small-cell lung cancer (NSCLC). However, data on clinical predictive factors remain scarce.

Objective: We aim to identify clinical biomarkers in patients undergoing chemoimmunotherapy.

Methods: This multicenter, real-world cohort study included chemonaive patients who underwent chemoimmunotherapy between December 2018 and May 2022. Multivariate analysis was used to determine associations between survival outcomes and patient background, including baseline neutrophil-to-lymphocyte ratio (NLR) and its dynamic change (ΔNLR). To further investigate the clinical significance of NLR, patients were classified based on their peripheral immune status, defined by a combination of NLR and ΔNLR.

Results: The study included 280 patients with 30.1 months of median follow-up. Multivariate analysis revealed that older individuals, poor performance status, tumor proportion score < 1%, liver metastasis, baseline NLR ≥ 5, and ΔNLR ≥ 0 independently correlated significantly with shorter progression-free and overall survival (OS). Patients with high peripheral immune status (defined as NLR <5 and ΔNLR < 0) significantly improved long-term survival (2-year OS rate of 58.3%), whereas those with low peripheral immune status (defined as NLR ≥ 5 and ΔNLR ≥ 0) had extremely poor outcomes (2-year OS rate of 5.6%). Safety profiles did not differ significantly in terms of severe adverse events and treatment-related death rates despite the patients' peripheral immune status (P = 0.46 and 0.63, respectively).

Conclusions: Our study provides real-world evidence regarding clinical prognostic factors for the efficacy of chemoimmunotherapy. The combined assessment of baseline NLR and ΔNLR could facilitate the identification of patients who are likely to achieve a durable response from chemoimmunotherapy.

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来源期刊
Targeted Oncology
Targeted Oncology 医学-肿瘤学
CiteScore
8.40
自引率
3.70%
发文量
64
审稿时长
>12 weeks
期刊介绍: Targeted Oncology addresses physicians and scientists committed to oncology and cancer research by providing a programme of articles on molecularly targeted pharmacotherapy in oncology. The journal includes: Original Research Articles on all aspects of molecularly targeted agents for the treatment of cancer, including immune checkpoint inhibitors and related approaches. Comprehensive narrative Review Articles and shorter Leading Articles discussing relevant clinically established as well as emerging agents and pathways. Current Opinion articles that place interesting areas in perspective. Therapy in Practice articles that provide a guide to the optimum management of a condition and highlight practical, clinically relevant considerations and recommendations. Systematic Reviews that use explicit, systematic methods as outlined by the PRISMA statement. Adis Drug Reviews of the properties and place in therapy of both newer and established targeted drugs in oncology.
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