Schlam I, Loi S, Salgado R, Swain S M
Department of Medical Oncology, Dana Farber Cancer Institute, Boston, USA; Harvard Medical School, Boston, USA. Electronic address: https://twitter.com/ilanaschlam.
Peter Mac Callum Cancer Centre, Melbourne, Victoria, Australia. Electronic address: https://twitter.com/LoiSher.
ESMO Open. 2025 Feb;10(2):104120. doi: 10.1016/j.esmoop.2024.104120. Epub 2025 Jan 17.
In this review, we evaluate the role of stromal tumor-infiltrating lymphocytes (sTILs) as a biomarker in human epidermal growth factor receptor 2 (HER2)-positive breast cancer, exploring the prognostic and predictive potential in various treatment settings.
Data from multiple clinical trials in the early and metastatic settings, focusing on TILs' correlation with pathologic complete response (pCR), progression-free survival (PFS), and overall survival across early and metastatic HER2-positive breast cancer were summarized. This review also discusses TILs' assessment methods, interobserver variability, and emerging technologies to assess TILs.
TILs have been identified as a highly reproducible biomarker that predicts pCR in patients receiving neoadjuvant therapy and serves as a prognostic indicator for long-term outcomes in several breast cancer subtypes, including HER2-positive. Studies indicate that higher TIL levels correlate with better recurrence-free survival rates. Despite these findings, there is no consensus on the optimal TIL threshold for clinical decision making, and further research is required on how to incorporate TILs into routine clinical practice.
TILs represent a promising biomarker in HER2-positive breast cancer, particularly in early disease settings. This assessment could guide treatment de-escalation or intensification, tailoring therapies to individual patient profiles. Due to their prognostic importance, TILs can be added to pathology reports. However, further validation in clinical trials is essential for the widespread adoption of TILs in clinical practice.
在本综述中,我们评估基质肿瘤浸润淋巴细胞(sTILs)作为人表皮生长因子受体2(HER2)阳性乳腺癌生物标志物的作用,探讨其在各种治疗环境中的预后和预测潜力。
总结了早期和转移性环境中多项临床试验的数据,重点关注TILs与病理完全缓解(pCR)、无进展生存期(PFS)以及早期和转移性HER2阳性乳腺癌总生存期的相关性。本综述还讨论了TILs的评估方法、观察者间的变异性以及评估TILs的新兴技术。
TTILsTILs已被确定为一种高度可重复的生物标志物,可预测接受新辅助治疗患者的pCR,并作为包括HER2阳性在内的几种乳腺癌亚型长期预后的指标。研究表明,较高的TIL水平与更好的无复发生存率相关。尽管有这些发现,但对于临床决策的最佳TIL阈值尚无共识,关于如何将TILs纳入常规临床实践还需要进一步研究。
TILs是HER2阳性乳腺癌中一种有前景的生物标志物,尤其是在早期疾病环境中。这种评估可以指导治疗的降级或强化,根据个体患者情况量身定制治疗方案。由于其预后重要性,TILs可以添加到病理报告中。然而,在临床试验中进行进一步验证对于TILs在临床实践中的广泛应用至关重要。