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弥漫性大B细胞淋巴瘤(DLBCL)患者中乳酸脱氢酶(LDH)与绝对淋巴细胞计数比值高预示着肿瘤内免疫反应差和生存期短。

A high LDH to absolute lymphocyte count ratio in patients with DLBCL predicts for a poor intratumoral immune response and inferior survival.

作者信息

Keane Colm, Tobin Joshua, Talaulikar Dipti, Green Michael, Crooks Pauline, Jain Sanjiv, Gandhi Maher

机构信息

University of Queensland Diamantina Institute, Translational Research Institute, University of Queensland, Brisbane, Queensland, Australia.

Princess Alexandra Hospital, Brisbane, Queensland, Australia.

出版信息

Oncotarget. 2018 May 4;9(34):23620-23627. doi: 10.18632/oncotarget.25306.

Abstract

PURPOSE

To test the utility of the circulating Lactate Dehydrogenase (LDH) to absolute lymphocyte count (ALC) ratio (LAR) to predict outcome to conventional first-line chemo-immunotherapy in Diffuse Large B-cell Lymphoma (DLBCL), and investigate its correlation to the tumour immune microenvironment (TME).

EXPERIMENTAL DESIGN

A population based cohort of 210 patients (median age: 64, range 18-90 years) with median follow up 3.8 years was analysed. All patients were treated with R-CHOP, and no immunosuppression related cases were included. Tissue for nanoString gene expression was available in 141.

RESULTS

High (i.e. adverse) LAR was associated with inferior progression free and overall survival (PFS 45% vs. 78%; OS 56% vs 86%, both p<0.001) at 5-years. Patients with a high LAR had a strikingly different TME compared to patients with a low ratio. Low LAR was associated with a good-risk TME immune gene signature (p<0.0001), including high CD8 and lower M2 macrophage infiltration. COO classification was not significantly different between high and low LAR patients. LAR was predictive of outcome independent of cell of origin and the international prognostic index (IPI). In particular, LAR discriminated patients with high IPI (3-5), showing 5-year PFS and OS of 32% vs. 74% (p=0.0006), and 43% vs. 81% (p=0.0003). A combined nanoString based immune score and the LAR allowed better prediction of outcome than either prognosticator alone (p<0.0001).

CONCLUSIONS

The LAR reflects the TME within DLBCL, and is a strong predictor of outcome in DLBCL treated with conventional first-line therapy that is independent of and additive to the IPI. Further studies are required to determine if this easily applicable blood assay can determine patients that might benefit from immune checkpoint blockade.

摘要

目的

检测循环乳酸脱氢酶(LDH)与绝对淋巴细胞计数(ALC)比值(LAR)在预测弥漫性大B细胞淋巴瘤(DLBCL)患者接受传统一线化疗免疫治疗疗效方面的实用性,并研究其与肿瘤免疫微环境(TME)的相关性。

实验设计

分析了一个基于人群的队列,共210例患者(中位年龄:64岁,范围18 - 90岁),中位随访时间为3.8年。所有患者均接受R-CHOP治疗,不包括免疫抑制相关病例。141例患者有可用于纳米孔基因表达分析的组织。

结果

高(即不良)LAR与5年时较差的无进展生存期(PFS 45%对78%;OS 56%对86%,p均<0.001)相关。与低LAR患者相比,高LAR患者的TME明显不同。低LAR与良好风险的TME免疫基因特征相关(p<0.0001),包括高CD8和较低的M2巨噬细胞浸润。高LAR和低LAR患者之间的COO分类无显著差异。LAR可独立于起源细胞和国际预后指数(IPI)预测疗效。特别是,LAR区分了高IPI(3 - 5)患者,其5年PFS和OS分别为32%对74%(p = 0.0006),以及43%对81%(p = 0.0003)。基于纳米孔的免疫评分与LAR联合使用比单独使用任何一种预后指标能更好地预测疗效(p<0.0001)。

结论

LAR反映了DLBCL中的TME,是接受传统一线治疗的DLBCL患者疗效的有力预测指标,独立于IPI且可作为其补充。需要进一步研究以确定这种易于应用的血液检测是否能确定可能从免疫检查点阻断中获益 的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b9/5955090/7e34eb34ff3c/oncotarget-09-23620-g001.jpg

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