1 Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, VIC, Australia.
2 Gustave Roussy, Université Paris-Saclay, Villejuif, France.
J Clin Oncol. 2019 Mar 1;37(7):559-569. doi: 10.1200/JCO.18.01010. Epub 2019 Jan 16.
The aim of the current study was to conduct a pooled analysis of studies that have investigated the prognostic value of tumor-infiltrating lymphocytes (TILs) in early-stage triple negative breast cancer (TNBC).
Participating studies had evaluated the percentage infiltration of stromally located TILs (sTILs) that were quantified in the same manner in patient diagnostic samples of early-stage TNBC treated with anthracycline-based chemotherapy with or without taxanes. Cox proportional hazards regression models stratified by trial were used for invasive disease-free survival (iDFS; primary end point), distant disease-free survival (D-DFS), and overall survival (OS), fitting sTILs as a continuous variable adjusted for clinicopathologic factors.
We collected individual data from 2,148 patients from nine studies. Average age was 50 years (range, 22 to 85 years), and 33% of patients were node negative. The average value of sTILs was 23% (standard deviation, 20%), and 77% of patients had 1% or more sTILs. sTILs were significantly lower with older age ( P = .001), larger tumor size ( P = .01), more nodal involvement ( P = .02), and lower histologic grade ( P = .001). A total of 736 iDFS and 548 D-DFS events and 533 deaths were observed. In the multivariable model, sTILs added significant independent prognostic information for all end points (likelihood ratio χ, 48.9 iDFS; P < .001; χ, 55.8 D-DFS; P < .001; χ, 48.5 OS; P < .001). Each 10% increment in sTILs corresponded to an iDFS hazard ratio of 0.87 (95% CI, 0.83 to 0.91) for iDFS, 0.83 (95% CI, 0.79 to 0.88) for D-DFS, and 0.84 (95% CI, 0.79 to 0.89) for OS. In node-negative patients with sTILs ≥ 30%, 3-year iDFS was 92% (95% CI, 89% to 98%), D-DFS was 97% (95% CI, 95% to 99%), and OS was 99% (95% CI, 97% to 100%).
This pooled data analysis confirms the strong prognostic role of sTILs in early-stage TNBC and excellent survival of patients with high sTILs after adjuvant chemotherapy and supports the integration of sTILs in a clinicopathologic prognostic model for patients with TNBC. This model can be found at www.tilsinbreastcancer.org .
本研究旨在对评估肿瘤浸润淋巴细胞(TILs)在早期三阴性乳腺癌(TNBC)中的预后价值的研究进行汇总分析。
参与研究评估了早期接受蒽环类化疗联合或不联合紫杉烷的 TNBC 患者诊断样本中间质 TILs(sTILs)百分比浸润情况。采用按试验分层的 Cox 比例风险回归模型,对无侵袭性疾病生存(iDFS;主要终点)、远处无病生存(D-DFS)和总生存(OS)进行分析,sTILs 作为连续变量进行调整,以适应临床病理因素。
我们从 9 项研究中收集了 2148 名患者的个体数据。平均年龄为 50 岁(范围,2285 岁),33%的患者为淋巴结阴性。sTILs 的平均值为 23%(标准差,20%),77%的患者 sTILs 占比≥1%。sTILs 与年龄较大(P=0.001)、肿瘤较大(P=0.01)、淋巴结受累较多(P=0.02)和组织学分级较低(P=0.001)显著相关。共观察到 736 例 iDFS 事件、548 例 D-DFS 事件和 533 例死亡事件。在多变量模型中,sTILs 为所有终点提供了显著的独立预后信息(似然比χ²,48.9 iDFS;P<0.001;χ²,55.8 D-DFS;P<0.001;χ²,48.5 OS;P<0.001)。sTILs 每增加 10%,iDFS 的风险比为 0.87(95%CI,0.830.91),D-DFS 的风险比为 0.83(95%CI,0.790.88),OS 的风险比为 0.84(95%CI,0.790.89)。在 sTILs≥30%的淋巴结阴性患者中,3 年 iDFS 为 92%(95%CI,89%98%),D-DFS 为 97%(95%CI,95%99%),OS 为 99%(95%CI,97%~100%)。
这项汇总数据分析证实了 sTILs 在早期 TNBC 中的强烈预后作用,以及接受辅助化疗后高 sTILs 患者的良好生存,并支持将 sTILs 纳入 TNBC 患者的临床病理预后模型中。该模型可在 www.tilsinbreastcancer.org 找到。