淋巴细胞/单核细胞比值在不可切除胆道癌接受全身化疗患者中的预后意义。

Cancer diagnosis & prognosis Pub Date : 2025-01-03 eCollection Date: 2025-01-01 DOI:10.21873/cdp.10422
Hideo Suzuki, Akifumi Kuwano, Junro Takahira, Kosuke Tanaka, Masayoshi Yada, Kenta Motomura
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引用次数: 0

摘要

背景/目的:胆道肿瘤(BTC)的发病率,包括胆管癌和胆囊癌,在世界范围内呈上升趋势。大约70%的BTC患者在诊断时已处于疾病晚期,导致生存率较低。最近的临床试验表明,在吉西他滨+顺铂化疗中加入免疫检查点抑制剂,如杜伐单抗或派姆单抗,可显著提高生存率,使三联疗法成为目前BTC一线治疗的标准。对比特币具有预测价值的模型很少。淋巴细胞与单核细胞比值(LMR)是一种相对较新的炎症相关评分和转化生物标志物,对其他癌症患者的生存具有预后价值。本研究评估了LMR对晚期BTC患者的预后价值,并分析了与总生存期(OS)相关的危险因素。患者和方法:这项前瞻性研究纳入了日本Aso Iizuka医院接受吉西他滨化疗的75例晚期BTC患者。LMR预测6个月生存的临界值为3.27。结果:与低LMR患者相比,高LMR患者的OS时间更长(中位分别为32.4个月和8.6个月;p = 0.0069)。多因素分析发现LMR >3.27[危险比(HR)=0.427, p=0.0339]和客观有效率(HR=0.210, p=0.0116)是影响OS的独立因素。结论:尽管存在一些局限性,如单中心设计和小样本量,但本研究的结果表明,LMR在预测接受吉西他滨化疗的BTC患者的生存结局方面具有潜在的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic Significance of Lymphocyte-to-Monocyte Ratio in Patients With Unresectable Biliary Tract Cancer Undergoing Systemic Chemotherapy.

Background/aim: The incidence of biliary tract cancers (BTC), including cholangiocarcinoma and gallbladder cancer, has been increasing worldwide. Approximately 70% of BTC patients have advanced disease at diagnosis, leading to a poor survival rate. Recent clinical trials have demonstrated that the addition of immune checkpoint inhibitors, such as durvalumab or pembrolizumab, to gemcitabine plus cisplatin chemotherapy significantly improves survival rates, making triple therapy the current standard for first-line treatment of BTC. Few models with predictive value exist for BTC. Lymphocyte-to-monocyte ratio (LMR) is a relatively new inflammation-related score and translational biomarker and has prognostic value for survival of patients with other cancers. This study assessed the prognostic value of LMR in patients with advanced BTC and analyzed the risk factors associated with overall survival (OS).

Patients and methods: This prospective study enrolled 75 patients with advanced BTC who were treated with gemcitabine-based chemotherapies at Aso Iizuka Hospital, Japan. The cutoff value of LMR for predicting 6-month survival was 3.27.

Results: OS was longer for patients with high LMR compared with low LMR (median 32.4 months and 8.6 months, respectively; p=0.0069). Multivariate analysis identified LMR >3.27 [hazard ratio (HR)=0.427, p=0.0339] and objective response rate (HR=0.210, p=0.0116) as independent factors associated with OS.

Conclusion: Despite some limitations, such as the single-center design and small sample size, the results of this study suggest a potential role for LMR in predicting survival outcomes for BTC patients treated with gemcitabine-based chemotherapies.

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