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TIL(肿瘤浸润淋巴细胞)对乳腺癌新辅助治疗反应与预后的预测价值:基于中国人群的多中心回顾性研究

英文原题:Predictive value of tumor-infiltrating lymphocytes for neoadjuvant therapy response and prognosis in breast cancer: a multicenter retrospective study based on Chinese population.

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Predictive value of tumor-infiltrating lymphocytes for neoadjuvant therapy response and prognosis in breast cancer: a multicenter retrospective study based on Chinese population.

PubMed 2025/10/15(内容时间) BMC Cancer Q2 · IF 4.1(JCR 2025)

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研究概要

TIL 可作为 pCR 的独立预测因素。

中文摘要

本研究旨在考察TIL(肿瘤浸润淋巴细胞)对乳腺癌患者新辅助治疗应答和长期预后的预测价值及最佳截断值。

纳入2013年1月至2023年12月在上海交通大学医学院附属瑞金医院及福建医科大学附属泉州第一医院确诊并接受新辅助化疗(NAC)的原发性乳腺癌患者。依据国际免疫肿瘤生物标志物工作组指南,在NAC前乳腺肿瘤组织中评估TIL。采用限制性立方样条(RCS)回归分析连续变量TIL与病理完全缓解(pCR)及预后的潜在非线性关系。通过Logistic回归考察TIL与pCR的关联,并用Cox比例风险回归评估其对乳腺癌无复发间期(BCFI)和总生存期(OS)的影响。

共纳入424例患者,中位随访95个月。RCS分析显示,TIL 10%是本队列预测pCR的最佳截断值。147例患者(34.7%)TIL较高(定义为>10%)。TIL较高患者pCR率显著更高(29.3%),而TIL较低者为8.7%(P<.001)。高TIL患者达到pCR的OR为0.29(95% CI 0.16–0.52,P<.001)。此外,多变量分析显示,低TIL患者乳腺癌复发风险显著升高(HR 2.36,95% CI 1.47–3.80,P<.001)。单变量Cox回归显示,低TIL表达显著降低OS(HR 2.22,95% CI 1.17–4.19,P=.014),多变量分析中也呈较差趋势。三阴性乳腺癌(TNBC)患者TIL较高与BCFI和OS改善相关;激素受体阳性、HER2阴性肿瘤中未见显著关联。

TIL可作为pCR的独立预测因子。结果也支持TIL作为TNBC和HER2阳性乳腺癌的长期预后指标,但不适用于HR阳性/HER2阴性亚型。

展开英文摘要原文

This study aims to investigate the predictive value and optimal threshold of tumor-infiltrating lymphocytes (TILs) for neoadjuvant treatment response and long-term prognosis in breast cancer patients.

Patients with primary breast cancer who were diagnosed and received neoadjuvant chemotherapy (NAC) at Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine and Quanzhou First Hospital affiliated to Fujian Medical University between January 2013 and December 2023 were included. The assessment of TILs was performed on pre-NAC breast tumor tissue according to the guidelines of the International Immuno-Oncology Biomarker Working Group. Restricted cubic spline (RCS) regression was used to explore the potential nonlinear relationships between the continuous variable TILs and pathological complete response (pCR) as well as prognosis. Logistic regression was used to examine the association between TILs and pCR, and Cox proportional hazards regression assessed the effects on breast cancer-free interval (BCFI) and overall survival (OS).

In this study, a total of 424 patients were included in the analysis. Median follow-up time was 95 months. RCS analysis indicated that a TILs threshold of 10% is the optimal cutoff for predicting pCR in this cohort. Among the participants, 147 patients (34.7%) exhibited high TIL expression, defined as > 10%. Notably, the pCR rate was significantly higher in patients with Elevated TIL levels, achieving 29.3% compared to only 8.7% in those with lower TIL levels (p < 0.001). The odds ratio (OR) for achieving pCR in patients with high TILs was 0.29, with a 95% confidence interval (CI) of 0.16 to 0.52 (p < 0.001). Furthermore, multivariate analysis revealed that patients with low TIL levels are at a substantially increased risk of breast cancer recurrence, with a hazard ratio (HR) of 2.36 (95% CI: 1.47 3.80, p < 0.001). Univariate Cox regression analysis showed that low TIL expression significantly compromised OS (HR: 2.22, 95% CI: 1.17 4.19, p = 0.014), while a trend towards worse in multivariate analysis. In addition, high TIL levels were associated with improved BCFI and OS in triple-negative breast cancer (TNBC) patients; however, no significant relationship was observed in hormone receptor-positive, HER2-negative tumors.

TILs could serve as an independent predictor of pCR. Our results also support TILs as long-term prognostic predictors for TNBC and HER2-positive breast cancers, but not for HR + HER2- subtype.

论文信息

作者
Li L、Yang P、Hong C、Chen D、Lian W
第一作者单位
Department of Breast Surgery, Affiliated Quanzhou First Hospital of Fujian Medical University, Quanzhou, Fujian, 362000, P.R. China.China
通讯作者单位
Department of Breast Surgery, Affiliated Quanzhou First Hospital of Fujian Medical University, Quanzhou, Fujian, 362000, P.R. China. weibinlian@fjmu.edu.cn.China
文献类型
多中心研究
期刊
BMC cancer2025 Oct 15
原文标识
PubMed 41094431 · DOI 10.1186/s12885-025-15022-x