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全身炎症反应指数(SIRI)与 CD8⁺ TIL(肿瘤浸润淋巴细胞)对局限性软组织未分化多形性肉瘤患者的预后价值

英文原题:The prognostic value of systemic inflammatory response index (SIRI) and CD8 + tumor-infiltrating lymphocytes for patients with localized undifferentiated pleomorphic sarcoma of soft tissue.

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The prognostic value of systemic inflammatory response index (SIRI) and CD8 + tumor-infiltrating lymphocytes for patients with localized undifferentiated pleomorphic sarcoma of soft tissue.

PubMed 2025/12/15(内容时间) BMC Cancer Q2 · IF 4.1(JCR 2025)

研究概要

在局限性UPS患者中,CD8 + TILs浸润至肿瘤组织可改善高SIRI患者的预后。

研究思路结论见上方概要

炎症血液标志物和TIL(肿瘤浸润淋巴细胞)(TILs)与多种癌症的预后相关。然而,关于它们作为软组织未分化多形性肉瘤(UPS)预后标志物价值的报道有限。我们旨在阐明这些标志物对UPS患者预后的预测价值,重点关注四肢和躯干可切除肿瘤。

本回顾性分析纳入103例四肢和躯干局限性UPS患者的数据。计算中性粒细胞-淋巴细胞比值(NLR)、血小板-淋巴细胞比值(PLR)、淋巴细胞-单核细胞比值(LMR)和全身炎症反应指数(SIRI),并以中位值作为截断值。同时进行CD8 + TIL的免疫组化染色。采用Kaplan-Meier法分析疾病特异性总生存(DOS)率和无远处转移生存(DMFS)率,并采用Cox比例风险模型确定预后因素。

在炎症血液标志物中,SIRI被发现是一个敏感的预后因素,高SIRI与较差的DOS(P = 0.16)和DMFS(P = 0.09)相关。尽管CD8 + TILs与DOS无关(P = 0.67),但高CD8 + TILs与改善的DMFS相关(P = 0.20)。在单变量分析中,只有肿瘤大小 > 10 cm与较差的DMFS显著相关(P = 0.02),而炎症血液标志物和CD8 + TIL显示无相关性。SIRI与CD8 + TILs的联合分析显示,与低CD8 + TILs且高SIRI的患者相比,高SIRI患者中肿瘤组织高CD8 + TILs可改善DMFS(P = 0.04)和DOS(P = 0.15)。

展开英文摘要原文

BACKGROUND: Inflammatory blood markers and tumor-infiltrating lymphocytes (TILs) are associated with the prognosis of various cancers. However, reports on their value as prognostic markers in soft tissue undifferentiated pleomorphic sarcoma (UPS) are limited. We aimed to clarify the predictive value of these markers for the prognosis of patients with UPS, focusing on resectable tumors of the extremities and trunk. METHODS: This retrospective analysis included data from 103 patients with localized UPS in the extremities and trunk. The neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), lymphocyte-monocyte ratio (LMR), and systemic inflammatory response index (SIRI) were calculated, and the median values were determined as cut-off values. Immunohistochemical staining of CD8 + TILs was also performed. Disease-specific overall survival (DOS) and distant metastasis-free survival (DMFS) rates were analyzed using the Kaplan-Meier method, and prognostic factors were identified using the Cox proportional hazards model. RESULTS: Among the inflammatory blood markers, SIRI was found to be a sensitive prognostic factor, and a high SIRI was associated with worse DOS (P = 0.16) and DMFS (P = 0.09). Although CD8 + TILs were not associated with DOS (P = 0.67), high CD8 + TILs correlated with improved DMFS (P = 0.20). Only tumor size > 10 cm was significantly associated with worse DMFS (P = 0.02) in the univariate analysis, while inflammatory blood markers and CD8 + TIL showed no correlation. The combination of SIRI and CD8 + TILs revealed that high CD8 + TILs in tumor tissue could improve DMFS (P = 0.04) and DOS (P = 0.15) in patients with high SIRI compared to those with low CD8 + TILs and high SIRI. CONCLUSIONS: In patients with localized UPS, CD8 + TILs infiltration into the tumor tissue could improve the prognosis of patients with high SIRI.

论文信息

作者
Kobayashi H、Abe H、Ushiku T、Nezu Y、Hiruma T、Iwata S、Kawai A、Mori T
单位
Department of Orthopaedic Surgery, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan. hkobayashi-tky@umin.ac.jp.Japan
期刊
BMC cancer2025 Dec 15
原文标识
PubMed 41398940 · DOI 10.1186/s12885-025-15182-w