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接受检查点抑制剂治疗的实体瘤患者选择的临床特征和影像预测结果。

Clinical characteristics of patient selection and imaging predictors of outcome in solid tumors treated with checkpoint-inhibitors.

机构信息

Medical Oncology, Humanitas Clinical and Research Hospital, Rozzano, Italy.

Nuclear Medicine, Humanitas Clinical and Research Hospital, Rozzano, Italy.

出版信息

Eur J Nucl Med Mol Imaging. 2017 Dec;44(13):2310-2325. doi: 10.1007/s00259-017-3802-5. Epub 2017 Aug 16.

Abstract

The rapidly evolving knowledge on tumor immunology and the continuous implementation of immunotherapy in cancer have recently led to the FDA and EMA approval of several checkpoint inhibitors as immunotherapic agents in clinical practice. Anti-CTLA-4, anti-PD-1, and anti-PDL-1 antibodies are becoming standard of care in advanced melanoma, as well as in relapsed or metastatic lung and kidney cancer, demonstrating higher and longer response compared to standard chemotherapy. These encouraging results have fostered the evaluation of these antibodies either alone or in combination with other therapies in several dozen clinical trials for the treatment of multiple tumor types. However, not all patients respond to immune checkpoint inhibitors, hence, specific biomarkers are necessary to guide and monitor therapy. The utility of PD-L1 expression as a biomarker has varied in different clinical trials, but, to date, no consensus has been reached on whether PD-L1 expression is an ideal marker for response and patient selection; approximately 20-25% of patients will respond to immunotherapy with checkpoint inhibitors despite a negative PD-L1 staining. On the other hand, major issues concern the evaluation of objective response in patients treated with immunotherapy. Pure morphological criteria as commonly used in solid tumors (i.e. RECIST) are not sufficient because change in size is not an early and reliable marker of tumor response to biological therapies. Thus, the scientific community has required a continuous adaptation of immune-related response criteria (irRC) to overcome the problem. In this context, metabolic information and antibody-based imaging with positron emission tomography (PET) have been investigated, providing a powerful approach for an optimal stratification of patients at staging and during the evaluation of the response to therapy. In the present review we provide an overview on the clinical characteristics of patient selection when using imaging predictors of outcome in solid tumors treated with checkpoint-inhibitors.

摘要

肿瘤免疫学领域的知识不断发展,免疫疗法在癌症治疗中的应用不断推进,最近已促使美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准了几种检查点抑制剂作为免疫治疗药物在临床实践中应用。抗 CTLA-4、抗 PD-1 和抗 PD-L1 抗体已成为晚期黑色素瘤以及复发性或转移性肺癌和肾癌的标准治疗方法,与标准化疗相比,这些药物具有更高的应答率和更长的应答持续时间。这些令人鼓舞的结果促使人们在数十项临床试验中评估这些抗体单独或与其他疗法联合用于治疗多种肿瘤类型。然而,并非所有患者对免疫检查点抑制剂均有应答,因此需要特定的生物标志物来指导和监测治疗。不同临床试验中 PD-L1 表达作为生物标志物的实用性存在差异,但迄今为止,尚未就 PD-L1 表达是否是预测应答和选择患者的理想标志物达成共识;尽管 PD-L1 染色阴性,约 20-25%的患者会对免疫检查点抑制剂治疗有应答。另一方面,主要问题涉及接受免疫治疗的患者的客观应答评估。在实体瘤中常用的纯形态学标准(即 RECIST)并不充分,因为大小的变化不是生物治疗的肿瘤应答的早期和可靠标志物。因此,科学界需要不断调整免疫相关反应标准(irRC)以克服这一问题。在这种情况下,代谢信息和基于抗体的正电子发射断层扫描(PET)成像已被研究,为在分期和评估治疗应答时对患者进行最佳分层提供了有力方法。在本综述中,我们概述了在使用成像预测标志物评估接受检查点抑制剂治疗的实体瘤患者的临床特征时的患者选择特点。

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