免疫检查点抑制剂治疗晚期肾细胞癌患者的基线炎症生物标志物与临床结果的关联

IF 4.2 2区 医学 Q2 ONCOLOGY Therapeutic Advances in Medical Oncology Pub Date : 2025-02-12 eCollection Date: 2025-01-01 DOI:10.1177/17588359251316243
Ahmet Yildirim, Mengting Wei, Yuan Liu, Bassel Nazha, Jacqueline T Brown, Bradley C Carthon, Yujin Choi, Lauren Suh, Rohit V Goswamy, Greta R McClintock, Caitlin Hartman, Sarah Caulfield, Jordan Ciuro, Jamie M Goldman, Wayne B Harris, Omer Kucuk, Viraj A Master, Mehmet A Bilen
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引用次数: 0

摘要

背景:免疫检查点抑制剂(ICIs)已成为转移性肾癌的主要治疗方法,在特定的患者亚组中显示出增强的结果和持久的反应。然而,确定治疗结果的可靠预后生物标志物仍然具有挑战性。目的:本研究旨在评估接受ICIs的转移性肾癌患者的基线炎症标志物与总生存期(OS)、无进展生存期(PFS)和临床获益(CB)之间的相关性。CB定义为病情稳定、部分缓解或完全缓解的患者。设计:回顾性、单中心研究。方法:回顾性分析2018年至2023年Emory Winship癌症研究所401例接受ICIs治疗的成年晚期肾癌患者。从基线血液样本中收集改良格拉斯哥预后评分(mGPS)、中性粒细胞与淋巴细胞(NLR)、单核细胞与淋巴细胞(MLR)、血小板与淋巴细胞(PLR)和中性粒细胞与嗜酸性粒细胞比率(NER)。结果:401例患者(中位年龄66岁;男性71%;21%黑人/非裔美国人),中位随访时间为43.0个月(95% CI, 36.6-51.4)。mGPS评分为0分的患者比评分为1分的患者生存期更长(风险比(HR), 0.38;95% ci, 0.23-0.62;p p = 0.001),与mGPS评分为1分的患者相比,PFS更长(HR, 0.66;95% ci, 0.44-0.98;p = 0.039)和2 (HR, 0.44;95% ci, 0.29-0.67;p = 0.032)。低基线MLR与改善OS相关(HR, 0.60;95% ci, 0.44-0.83;p = 0.002)和PFS (HR, 0.73;95% ci, 0.55-0.97;p = 0.031)。同样,低基线PLR与较高的CB可能性相关(优势比(OR), 2.20;95% ci, 1.31-3.69;p = 0.003),低基线NER与改善OS相关(HR, 0.63;95% ci, 0.46-0.87;p = 0.004), PFS (HR, 0.67;95% ci, 0.51-0.88;p = 0.003),较高的CB (OR, 2.04;95% ci, 1.20-3.46;p = 0.008)。结论:较低水平的全身炎症标志物与ICI治疗更有利的临床结果相关。需要前瞻性研究来进一步验证。
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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Association of baseline inflammatory biomarkers and clinical outcomes in patients with advanced renal cell carcinoma treated with immune checkpoint inhibitors.

Background: Immune checkpoint inhibitors (ICIs) have become the mainstay treatment of metastatic kidney cancer, demonstrating enhanced outcomes and durable responses in select patient subgroups. However, identifying reliable prognostic biomarkers for treatment outcomes remains challenging.

Objectives: This study aimed to assess the correlation between baseline inflammatory markers and overall survival (OS), progression-free survival (PFS), and clinical benefit (CB) in metastatic kidney cancer patients receiving ICIs. CB was defined as patients achieving stable disease, partial response, or complete response.

Design: Retrospective, single-center study.

Methods: A retrospective analysis was conducted on 401 adult patients with advanced kidney cancer treated with ICIs at Emory Winship Cancer Institute between 2018 and 2023. Modified Glasgow Prognostic Score (mGPS), neutrophil-to-lymphocyte (NLR), monocyte-to-lymphocyte (MLR), platelet-to-lymphocyte (PLR), and neutrophil-to-eosinophil ratios (NER) were collected from baseline blood samples.

Results: Among 401 patients (median age, 66; 71% male; 21% Black/African American), median follow-up was 43.0 months (95% CI, 36.6-51.4). Patients with mGPS scores of 0 had longer OS than those with a score of 1 (hazard ratio (HR), 0.38; 95% CI, 0.23-0.62; p < 0.001) and 2 (HR, 0.37; 95% CI, 0.20-0.67; p = 0.001), and longer PFS compared to patients with mGPS scores of 1 (HR, 0.66; 95% CI, 0.44-0.98; p = 0.039) and 2 (HR, 0.44; 95% CI, 0.29-0.67; p < 0.001). Low baseline NLR was associated with longer PFS (HR, 0.73; 95% CI, 0.54-0.97; p = 0.032). Low baseline MLR correlated with improved OS (HR, 0.60; 95% CI, 0.44-0.83; p = 0.002) and PFS (HR, 0.73; 95% CI, 0.55-0.97; p = 0.031). Similarly, low baseline PLR was associated with higher CB likelihood (odds ratio (OR), 2.20; 95% CI, 1.31-3.69; p = 0.003), and low baseline NER was linked to improved OS (HR, 0.63; 95% CI, 0.46-0.87; p = 0.004), PFS (HR, 0.67; 95% CI, 0.51-0.88; p = 0.003), and higher CB (OR, 2.04; 95% CI, 1.20-3.46; p = 0.008).

Conclusion: Lower levels of systemic inflammatory markers are associated with more favorable clinical outcomes with ICI treatment. Prospective studies are needed for further validation.

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来源期刊
CiteScore
8.20
自引率
2.00%
发文量
160
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Medical Oncology is an open access, peer-reviewed journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of cancer. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in medical oncology, providing a forum in print and online for publishing the highest quality articles in this area. This journal is a member of the Committee on Publication Ethics (COPE).
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