Cao Bo, Zhang Ziran, Wang Chaoxian, Lv Xiang
Department of Breast Diseases, Jiaxing Maternity and Child Health Care Hospital, Affiliated Women and Children's Hospital of Jiaxing University, Jiaxing, Zhejiang 314000, P.R. China.
Oncol Lett. 2023 Aug 24;26(4):441. doi: 10.3892/ol.2023.14028. eCollection 2023 Oct.
Further adjuvant chemotherapy treatment can provide benefits to certain patients with triple-negative breast cancer (TNBC) that fail to achieve pathological complete response (pCR) after the administration of a neoadjuvant chemotherapy (NAC) regimen. However, biomarkers suitable for identifying patients likely to experience poor prognostic outcomes after undergoing additional adjuvant chemotherapy are currently lacking. Accordingly, the present meta-analysis was conducted to explore the relationship between tumor-infiltrating lymphocytes (TILs) or TIL subtypes (CD4 or CD8) in residual tumor (RT) tissue following NAC and TNBC patient prognosis. Relevant studies published through March 2023 were identified in Pubmed, The Cochrane Library, Embase and Web of Science databases. After excluding irrelevant studies, data were extracted from the remaining reports, while study quality was analyzed with the Newcastle-Ottawa Scale. Subsequent analyses were performed with Stata 14.0 and Review Manager 5.3. In total, seven relevant studies incorporating 1,202 patients were identified, all of which were retrospective cohort studies. Pooled analyses demonstrated that those patients exhibiting higher levels of RT TIL infiltration following NAC exhibited significantly improved recurrence-free, metastasis-free and event-free survival (RFS/MFS/EFS) compared with patients with lower RT TIL infiltration levels, together with an improved distant recurrence-free interval (DRFI) [hazard ratio (HR)=0.52; 95% confidence interval (CI)=0.39-0.69; P<0.00001]. In addition, patients exhibiting high RT TIL infiltration exhibited improved overall survival (OS) and breast cancer-specific survival (BCSS; HR=0.49; 95% CI=0.38-0.65; P<0.00001). Additional subgroup analyses revealed that patients with higher TIL infiltration levels or TIL subtype (CD4 or CD8) infiltration exhibited improved RFS/MFS/EFS/DRFI as compared with patients with lower levels of overall TIL or TIL subtype (CD4 or CD8) infiltration in RT tissue (HR=0.35, 95% CI=0.20-0.59, P<0.0001; HR=0.49, 95% CI=0.33-0.71, P=0.0002). Consistently, the OS/BCSS of patients exhibiting high levels of overall TIL or TIL subtype (CD4 or CD8) infiltration was increased compared with patients with lower levels of such infiltration (HR=0.33, 95% CI=0.19-0.59, P=0.0002; HR=0.55, 95% CI=0.41-0.76, P=0.0002). These data thus demonstrate that levels of overall TIL infiltration or infiltration by CD4 or CD8 TILs in RT following NAC can be used as a biomarker to reliably predict prognostic outcomes in patients with TNBC, in addition to highlighting possible targets that may guide the further immunotherapeutic management of these patients.
对于某些在接受新辅助化疗(NAC)方案后未达到病理完全缓解(pCR)的三阴性乳腺癌(TNBC)患者,进一步的辅助化疗可能有益。然而,目前缺乏适用于识别在接受额外辅助化疗后可能预后不良的患者的生物标志物。因此,本荟萃分析旨在探讨NAC后残留肿瘤(RT)组织中的肿瘤浸润淋巴细胞(TILs)或TIL亚型(CD4或CD8)与TNBC患者预后之间的关系。通过在Pubmed、Cochrane图书馆、Embase和Web of Science数据库中检索截至2023年3月发表的相关研究。在排除不相关研究后,从其余报告中提取数据,同时使用纽卡斯尔-渥太华量表分析研究质量。随后使用Stata 14.0和Review Manager 5.3进行分析。总共确定了7项纳入1202例患者的相关研究,所有这些研究均为回顾性队列研究。汇总分析表明,与RT TIL浸润水平较低的患者相比,NAC后RT TIL浸润水平较高的患者的无复发生存期、无转移生存期和无事件生存期(RFS/MFS/EFS)显著改善,同时远处无复发生存期(DRFI)也有所改善[风险比(HR)=0.52;95%置信区间(CI)=0.39-0.69;P<0.00001]。此外,RT TIL浸润水平高的患者的总生存期(OS)和乳腺癌特异性生存期(BCSS)有所改善(HR=0.49;95%CI=0.38-0.65;P<0.00001)。进一步的亚组分析显示,与RT组织中总体TIL或TIL亚型(CD4或CD8)浸润水平较低的患者相比,TIL浸润水平较高或TIL亚型(CD4或CD8)浸润的患者的RFS/MFS/EFS/DRFI有所改善(HR=0.35,95%CI=0.20-0.59,P<0.0001;HR=0.49,95%CI=0.33-0.71,P=0.0002)。同样,与浸润水平较低的患者相比,总体TIL或TIL亚型(CD4或CD8)浸润水平较高的患者的OS/BCSS有所增加(HR=0.33,95%CI=0.19-0.59,P=0.0002;HR=0.55,95%CI=0.41-0.76,P=0.0002)。因此,这些数据表明,NAC后RT中总体TIL浸润水平或CD4或CD8 TIL浸润水平可用作生物标志物,以可靠地预测TNBC患者的预后,此外还突出了可能指导这些患者进一步免疫治疗管理的潜在靶点。