Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
J Med Imaging Radiat Oncol. 2022 Jun;66(4):575-591. doi: 10.1111/1754-9485.13426. Epub 2022 May 17.
Immunotherapies have revolutionised cancer management. Despite their success, durable responses are limited to a subset of patients. Prediction of immunotherapy response in patients has proven to be difficult due to a lack of robust biomarkers. Routinely collected imaging may offer an additional information source to personalise patient treatment, with advantages over tissue-based biomarkers. Quantitative image analysis or radiomics, which involves the high-throughput extraction of imaging features, has the potential to non-invasively predict cancer histology, outcomes and prognosis. This review evaluates the value of radiomics in patients undergoing immunotherapy, with a summary provided of the performance of radiomics models in predicting immunotherapy response and toxicity, as well as immune correlates. Much of the literature focussed on clinical endpoints and correlates to tissue biomarkers, particularly in lung cancer, while few studies investigated association with immune-related adverse events. Strengths of the studies included more frequent use of clinical trial datasets, homogenous patient cohorts and high-quality diagnostic scans. Limitations of the studies include heterogeneity in study methodology, lack of well-defined homogenous imaging datasets, limited open publishing of imaging datasets, coding and parameters used for radiomics signature development and limited use of external validation datasets. Future research should address the above limitations, as well as further explore the relationship between radiomics and immune-related adverse effects and less well-studied biological correlates such tumour mutational burden, and incorporate known clinical prognostic scores into radiomics models.
免疫疗法已经彻底改变了癌症的治疗方式。尽管免疫疗法取得了成功,但持久的疗效仅局限于一部分患者。由于缺乏可靠的生物标志物,预测患者对免疫疗法的反应一直很困难。常规采集的影像学资料可能为患者的个体化治疗提供额外的信息来源,其具有优于组织生物标志物的优势。定量图像分析或放射组学涉及高通量提取影像学特征,具有非侵入性预测癌症组织学、结果和预后的潜力。这篇综述评估了放射组学在接受免疫治疗的患者中的价值,总结了放射组学模型在预测免疫治疗反应和毒性以及免疫相关性方面的表现。大部分文献侧重于临床终点和与组织生物标志物的相关性,尤其是在肺癌中,而很少有研究探讨与免疫相关的不良事件的相关性。研究的优势在于更多地使用临床试验数据集、同质的患者队列和高质量的诊断扫描。研究的局限性包括研究方法的异质性、缺乏明确的同质影像学数据集、影像学数据集的公开出版有限、用于放射组学特征开发的编码和参数有限以及外部验证数据集的使用有限。未来的研究应该解决上述局限性,进一步探索放射组学与免疫相关的不良反应以及研究较少的生物学相关性(如肿瘤突变负荷)之间的关系,并将已知的临床预后评分纳入放射组学模型。