Luen Stephen J, Savas Peter, Fox Stephen B, Salgado Roberto, Loi Sherene
Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Vic, Australia.
Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Pathology. 2017 Feb;49(2):141-155. doi: 10.1016/j.pathol.2016.10.010. Epub 2016 Dec 31.
Breast cancer has not previously been considered a highly immunogenic cancer. Observations of tumour-infiltrating lymphocytes (TILs) in and around neoplastic cells in tumour samples, and associations with improved pathological complete response and clinical survival end points have changed our perspective on this. Lymphocytic infiltrates have long been observed in breast cancer; however, more recently, retrospective analysis of prospectively collected tissue samples from clinical trials has demonstrated the potential role of host immunosurveillance in influencing the biology of breast cancer. This association appears to be strongest in triple negative and HER2 positive breast cancer subtypes. Contrastingly, the association in luminal tumours is less clear, and is potentially limited by substantial tumoural heterogeneity. Several methodologies have been employed to quantify, and describe the composition of TILs, each with its own advantages and disadvantages. The results of these analyses have been generally consistent, and valuable efforts are currently underway to standardise the evaluation of TILs toward a universal approach. More technical methods of TIL characterisation remain important in the research setting. The evaluation of TILs becomes increasingly relevant with the emerging role of immunotherapy in breast cancer. Early phase trials of checkpoint blockade show promising results; however, it is likely that some patients will require combination treatments to maximise therapeutic benefits. Equally, some patients may not derive any benefit from immunotherapies. This underscores the importance of the development of relevant predictive biomarkers. As a key representative of the immune interaction between host and tumour, lymphocytic infiltrates are ideally placed for continued research into the determinants of immunogenicity, and response to immunotherapeutic approaches. In this review, we will discuss the current methodologies of evaluation, and the clinical relevance of TILs. Additionally, we discuss the emerging role of immunotherapy in breast cancer, and the future of TIL characterisation in this context.
乳腺癌以前并未被视为具有高度免疫原性的癌症。对肿瘤样本中肿瘤细胞内及周围的肿瘤浸润淋巴细胞(TILs)的观察,以及其与病理完全缓解和临床生存终点改善之间的关联,改变了我们对此的看法。乳腺癌中淋巴细胞浸润现象早已被观察到;然而,最近对临床试验中前瞻性收集的组织样本进行的回顾性分析表明,宿主免疫监视在影响乳腺癌生物学行为方面具有潜在作用。这种关联在三阴性和HER2阳性乳腺癌亚型中似乎最为明显。相比之下,管腔型肿瘤中的关联尚不清楚,可能受到肿瘤显著异质性的限制。已经采用了几种方法来量化和描述TILs的组成,每种方法都有其自身的优缺点。这些分析结果总体上是一致的,目前正在进行有价值的努力,以使TILs的评估朝着通用方法标准化。在研究环境中,TILs更具技术性的表征方法仍然很重要。随着免疫疗法在乳腺癌中发挥越来越重要的作用,TILs的评估变得越来越重要。检查点阻断的早期试验显示出有希望的结果;然而,可能有些患者需要联合治疗以最大化治疗益处。同样,有些患者可能无法从免疫疗法中获得任何益处。这凸显了开发相关预测生物标志物的重要性。作为宿主与肿瘤之间免疫相互作用的关键代表,淋巴细胞浸润非常适合继续研究免疫原性的决定因素以及对免疫治疗方法的反应。在本综述中,我们将讨论当前的评估方法以及TILs的临床相关性。此外,我们还将讨论免疫疗法在乳腺癌中的新兴作用以及在此背景下TILs表征的未来。