Fatima Shadma, Ma Yafeng, Safrachi Azadeh, Haider Sana, Spring Kevin J, Vafaee Fatemeh, Scott Kieran F, Roberts Tara L, Becker Therese M, de Souza Paul
Department of Medical Oncology, Ingham Institute of Applied Medical Research, Liverpool, NSW 2170, Australia.
School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2031, Australia.
Cancers (Basel). 2022 Mar 25;14(7):1669. doi: 10.3390/cancers14071669.
Immunotherapy (IO), involving the use of immune checkpoint inhibition, achieves improved response-rates and significant disease-free survival for some cancer patients. Despite these beneficial effects, there is poor predictability of response and substantial rates of innate or acquired resistance, resulting in heterogeneous responses among patients. In addition, patients can develop life-threatening adverse events, and while these generally occur in patients that also show a tumor response, these outcomes are not always congruent. Therefore, predicting a response to IO is of paramount importance. Traditionally, tumor tissue analysis has been used for this purpose. However, minimally invasive liquid biopsies that monitor changes in blood or other bodily fluid markers are emerging as a promising cost-effective alternative. Traditional biomarkers have limitations mainly due to difficulty in repeatedly obtaining tumor tissue confounded also by the spatial and temporal heterogeneity of tumours. Liquid biopsy has the potential to circumvent tumor heterogeneity and to help identifying patients who may respond to IO, to monitor the treatment dynamically, as well as to unravel the mechanisms of relapse. We present here a review of the current status of molecular markers for the prediction and monitoring of IO response, focusing on the detection of these markers in liquid biopsies. With the emerging improvements in the field of liquid biopsy, this approach has the capacity to identify IO-eligible patients and provide clinically relevant information to assist with their ongoing disease management.
免疫疗法(IO),包括使用免疫检查点抑制剂,可为一些癌症患者提高缓解率并显著延长无病生存期。尽管有这些有益效果,但反应的可预测性较差,且存在较高的先天性或获得性耐药率,导致患者之间的反应存在异质性。此外,患者可能会出现危及生命的不良事件,虽然这些事件通常发生在也显示出肿瘤反应的患者中,但这些结果并不总是一致的。因此,预测对IO的反应至关重要。传统上,肿瘤组织分析一直用于此目的。然而,监测血液或其他体液标志物变化的微创液体活检正成为一种有前景的、具有成本效益的替代方法。传统生物标志物存在局限性,主要是由于难以反复获取肿瘤组织,同时肿瘤的空间和时间异质性也会造成干扰。液体活检有可能规避肿瘤异质性,有助于识别可能对IO有反应的患者,动态监测治疗情况,并揭示复发机制。我们在此对用于预测和监测IO反应的分子标志物的现状进行综述,重点关注在液体活检中检测这些标志物。随着液体活检领域的不断改进,这种方法有能力识别适合IO治疗的患者,并提供临床相关信息以协助其进行持续的疾病管理。