Mensali Nadia, Inderberg Else Marit
Translational Research Unit, Department of Cellular Therapy, Oslo University Hospital, 0379 Oslo, Norway.
Cancers (Basel). 2022 Apr 12;14(8):1940. doi: 10.3390/cancers14081940.
Immunotherapy has shown clinical benefits in several solid malignancies-in particular, melanoma and non-small cell lung cancer. However, in other solid tumours such as glioblastoma (GBM), the response to immunotherapy has been more variable, and except for anti-PD-1 for patients with microsatellite instable (MSI)+ cancers, no immunotherapy is currently approved for GBM patients. GBM is the most common and most aggressive brain cancer with a very poor prognosis and a median overall survival of 15 months. A few prognostic biomarkers have been identified and are used to some extent, but apart from MSI, no biomarkers are used for patient stratification for treatments other than the standard of care, which was established 15 years ago. Around 25% of new treatments investigated in GBM are immunotherapies. Recent studies indicate that the use of integrated and validated immune correlates predicting the response and guiding treatments could improve the efficacy of immunotherapy in GBM. In this review, we will give an overview of the current status of immunotherapy and biomarkers in use in GBM with the main challenges of treatment in this disease. We will also discuss emerging biomarkers that could be used in future immunotherapy strategies for patient stratification and potentially improved treatment efficacy.
免疫疗法已在多种实体恶性肿瘤中显示出临床益处,尤其是黑色素瘤和非小细胞肺癌。然而,在其他实体瘤如胶质母细胞瘤(GBM)中,免疫疗法的反应则更为多变,除了用于微卫星不稳定(MSI)+癌症患者的抗PD-1疗法外,目前尚无免疫疗法被批准用于GBM患者。GBM是最常见、侵袭性最强的脑癌,预后极差,中位总生存期为15个月。已经确定了一些预后生物标志物并在一定程度上得到应用,但除了MSI外,没有生物标志物用于除15年前确立的标准治疗之外的其他治疗的患者分层。在GBM中研究的新疗法约有25%是免疫疗法。最近的研究表明,使用综合且经过验证的免疫相关指标来预测反应并指导治疗,可能会提高GBM免疫疗法的疗效。在本综述中,我们将概述GBM中免疫疗法和生物标志物的现状以及该疾病治疗的主要挑战。我们还将讨论可用于未来免疫治疗策略中患者分层并可能提高治疗疗效的新兴生物标志物。