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局部晚期鼻咽癌患者中淋巴细胞-单核细胞比值、TIL(肿瘤浸润淋巴细胞)与肿瘤相关巨噬细胞同 3 年无进展生存期的相关性

英文原题:The Association Between Lymphocyte-Monocyte Ratio, Tumor-Infiltrating Lymphocytes, and Tumor-Associated Macrophages with 3-Year Progression-Free Survival in Advanced Local Stage Nasopharyngeal Cancer Patients.

查看英文原题

The Association Between Lymphocyte-Monocyte Ratio, Tumor-Infiltrating Lymphocytes, and Tumor-Associated Macrophages with 3-Year Progression-Free Survival in Advanced Local Stage Nasopharyngeal Cancer Patients.

PubMed 2026/06/21(内容时间) Cancer Invest Q3 · IF 2.2(JCR 2025)

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中文摘要

鼻咽癌(NPC)在印度尼西亚造成沉重疾病负担,亟需可靠预后生物标志物指导治疗决策。本研究考察淋巴细胞-单核细胞比值(LMR)、TIL(肿瘤浸润淋巴细胞)、肿瘤相关巨噬细胞(TAM)与晚期NPC患者3年无进展生存期(PFS)的关系。在一家国家级血液肿瘤转诊门诊建立回顾性队列,纳入2015年1月至2020年确诊患者。通过免疫组化评估TIL和TAM表达,并采用受试者工作特征分析确定LMR、CD8及CD163的截点。采用Kaplan-Meier法、log-rank检验及单变量和多变量Cox比例风险回归。3年PFS中位数为24个月(95% CI:19.44–25.04),3年无事件生存率为46.7%。

LMR较高(>1.82)和CD8⁺ TIL较高(>47.5%)者的3年PFS率(56.3%和59.3%)高于低值组(31.7%和30.4%)。CD163⁺ TAM较高(≥196)与3年PFS较差相关(9.1%比73.8%;p<0.001)。多变量模型中关联仍有统计学意义:LMR校正HR为1.844(p=0.026),CD8为2.222(p=0.008),CD163为5.680(p<0.0001)。在CD163模型中进一步校正年龄、ECOG体能状态、体重指数、治疗类型、性别及分期后,效应估计与单变量结果一致。这些生物标志物可能有助于晚期NPC风险分层。

展开英文摘要原文

Nasopharyngeal cancer (NPC) is a major health burden in Indonesia, and reliable prognostic biomarkers are needed to guide treatment decisions.

This study examined associations between lymphocyte-monocyte ratio (LMR), tumor-infiltrating lymphocytes (TILs), tumor-associated macrophages (TAMs), and 3-year progression-free survival (PFS) in advanced-stage NPC. A retrospective cohort was assembled at a national referral hematology-oncology clinic, including patients diagnosed from January 2015 to 2020. TIL and TAM expression were assessed by immunohistochemistry, and cutoffs for LMR, CD8, and CD163 were derived using receiver operating characteristic analysis. Kaplan-Meier methods with log-rank testing and Cox proportional hazards regression (univariable and multivariable) were applied. Median 3-year PFS was 24 months (95% CI: 19.

44-25. 04), with 46. 7% event-free at 3 years. High LMR (>1. 82) and high CD8+ TIL (>47. 5%) were associated with higher 3-year PFS (56. 3% and 59. 3%) than low groups (31. 7% and 30. 4%). High CD163+ TAM ( 196) was associated with worse 3-year PFS (9. 1% vs 73. 8%; p < 0. 001). In multivariable models, associations remained significant: LMR aHR 1.

844 ( p = 0. 026), CD8 aHR 2. 222 ( p = 0. 008), and CD163 aHR 5. 680 ( p < 0. 0001). After adjustment for age, ECOG, body mass index, treatment type, sex, and stage (CD163 model), effect estimates were consistent with univariable findings. These biomarkers may aid risk stratification in advanced NPC.

论文信息

作者
Dewi NPMP、Rachman A、Lisnawati L、Koesnoe S
第一作者单位
Department of Internal Medicine, Hematology and Oncology Division, Faculty of Medicine, Universitas Indonesia, Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.Indonesia
通讯作者单位
Department of Internal Medicine, Allergy and Immunology Division, Faculty of Medicine, Universitas Indonesia, Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.Indonesia
期刊
Cancer investigation2026 Sep
原文标识
PubMed 42324616 · DOI 10.1080/07357907.2026.2675655