抗血管生成和免疫肿瘤药物在转移性肾细胞癌(mRCC)中的成像反应:现状和未来挑战。

Laure Fournier, Alexandre Bellucci, Yann Vano, Mehdi Bouaboula, Constance Thibault, Reza Elaidi, Stephane Oudard, Charles Cuenod
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引用次数: 8

摘要

本报告旨在回顾抗血管生成和免疫肿瘤治疗下mRCC治疗评估的标准,并讨论成像师未来面临的挑战。RECIST标准似乎只能部分反映抗血管生成药物在mRCC中的临床获益。提出了新的分析方法来更好地评估对这些药物的反应,包括新的尺寸标准阈值(-10%),衰减(Choi和修改的Choi标准),功能成像技术(灌注CT,超声或MRI)和新的PET放射性示踪剂。进展成像是成像仪未来面临的主要挑战之一。是肿瘤的进展而不是反应会引发治疗的改变,因此应该通过成像技术来识别肿瘤的进展,以指导肿瘤学家选择最合适的时间来改变治疗。然而,人们对肿瘤进展的动力学知之甚少,还需要积累大量的数据来理解它。最后,随着免疫疗法的发展,观察到闪光或伪进展现象。需要进行研究,以确定影像学是否可以区分应继续治疗的假进展患者,或必须改变治疗的真进展患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Imaging Response of Antiangiogenic and Immune-Oncology Drugs in Metastatic Renal Cell Carcinoma (mRCC): Current Status and Future Challenges.

Imaging Response of Antiangiogenic and Immune-Oncology Drugs in Metastatic Renal Cell Carcinoma (mRCC): Current Status and Future Challenges.

Imaging Response of Antiangiogenic and Immune-Oncology Drugs in Metastatic Renal Cell Carcinoma (mRCC): Current Status and Future Challenges.

Imaging Response of Antiangiogenic and Immune-Oncology Drugs in Metastatic Renal Cell Carcinoma (mRCC): Current Status and Future Challenges.

This report aims to review criteria which have been proposed for treatment evaluation in mRCC under anti-angiogenic and immune-oncologic therapies and discuss future challenges for imagers. RECIST criteria seem to only partially reflect the clinical benefit derived from anti-angiogenic drugs in mRCC. New methods of analysis propose to better evaluate response to these drugs, including a new threshold for size criteria (-10%), attenuation (Choi and modified Choi criteria), functional imaging techniques (perfusion CT, ultrasound or MRI), and new PET radiotracers. Imaging of progression is one of the main future challenges facing imagers. It is progression and not response that will trigger changes in therapy, therefore it is tumour progression that should be identified by imaging techniques to guide the oncologist on the most appropriate time to change therapy. Yet little is known on dynamics of tumour progression, and much data still needs to be accrued to understand it. Finally, as immunotherapies develop, flare or pseudo-progression phenomena are observed. Studies need to be performed to determine whether imaging can distinguish between patients undergoing pseudo-progression for which therapy should be continued, or true progression for which the treatment must be changed.

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