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在靶向治疗药物和免疫治疗时代,使用氟代脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG PET/CT)进行黑色素瘤疗效评估的优势与挑战

The Advantages and Challenges of Using FDG PET/CT for Response Assessment in Melanoma in the Era of Targeted Agents and Immunotherapy.

作者信息

Wong Annie N M, McArthur Grant A, Hofman Michael S, Hicks Rodney J

机构信息

Cancer Medicine, The Peter MacCallum Cancer Centre, Melbourne, Australia.

The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Australia.

出版信息

Eur J Nucl Med Mol Imaging. 2017 Aug;44(Suppl 1):67-77. doi: 10.1007/s00259-017-3691-7. Epub 2017 Apr 7.

Abstract

The treatment of melanoma has been revolutionised in recent years by advances in the understanding of the genomic landscape of this disease, which has led to the development of new targeted therapeutic agents, and the ability to therapeutically manipulate the immune system through inhibition of cancer cell-T-cell interactions that prevent an adaptive immune response. While these therapeutic interventions have dramatically improved the prospects of survival for patients with advanced melanoma, they bring significant complexity to the interpretation of therapeutic response because their mechanisms and temporal profile of response vary considerably. In this review, we discuss the mode of action of these emerging therapies and their toxicities to provide a framework for the use of FDG PET/CT in therapeutic response assessment. We propose that the greatest utility of PET in assessment of response to agents that abrogate signalling related to BRAF mutation is for early assessment of resistance, while in anti-CTLA4 therapy, immunological flare can compromise early assessment of response but can identify potentially life-threatening autoimmune reactions. For anti-PD1/PDL1 therapy, the role of FDG PET/CT is more akin to its use in other solid malignancies undergoing treatment with conventional chemotherapy. However, further research is required to optimise the timing of scans and response criteria in this disease.

摘要

近年来,对黑色素瘤基因组格局认识的进展彻底改变了该疾病的治疗方式,这促成了新型靶向治疗药物的研发,以及通过抑制阻止适应性免疫反应的癌细胞与T细胞相互作用来对免疫系统进行治疗性调控的能力。虽然这些治疗干预措施显著改善了晚期黑色素瘤患者的生存前景,但它们给治疗反应的解读带来了极大的复杂性,因为其作用机制和反应的时间特征差异很大。在本综述中,我们讨论这些新兴疗法的作用方式及其毒性,以提供一个在治疗反应评估中使用FDG PET/CT的框架。我们提出,PET在评估针对与BRAF突变相关信号传导的药物反应时的最大效用在于早期评估耐药性,而在抗CTLA4治疗中,免疫反应增强可能会影响反应的早期评估,但可识别潜在的危及生命的自身免疫反应。对于抗PD1/PDL1治疗,FDG PET/CT的作用更类似于其在接受传统化疗的其他实体恶性肿瘤中的应用。然而,需要进一步研究以优化该疾病扫描的时间和反应标准。

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