Fred Hutchinson Cancer Research Center, Seattle, WA 98019, USA.
Magn Reson Imaging. 2012 Nov;30(9):1301-12. doi: 10.1016/j.mri.2012.06.009. Epub 2012 Aug 13.
Quantitative imaging using computed tomography, magnetic resonance imaging and positron emission tomography modalities will play an increasingly important role in the design of oncology trials addressing molecularly targeted, personalized therapies. The advent of molecularly targeted therapies, exemplified by antiangiogenic drugs, creates new complexities in the assessment of response. The Quantitative Imaging Network addresses the need for imaging modalities which can accurately and reproducibly measure not just change in tumor size but changes in relevant metabolic parameters, modulation of relevant signaling pathways, drug delivery to tumor and differentiation of apoptotic cell death from other changes in tumor volume. This article provides an overview of the applications of quantitative imaging to phase 0 through phase 3 oncology trials. We describe the use of a range of quantitative imaging modalities in specific tumor types including malignant gliomas, lung cancer, head and neck cancer, lymphoma, breast cancer, prostate cancer and sarcoma. In the concluding section, we discuss potential constraints on clinical trials using quantitative imaging, including complexity of trial conduct, impact on subject recruitment, incremental costs and institutional barriers. Strategies for overcoming these constraints are presented.
使用计算机断层扫描、磁共振成像和正电子发射断层扫描等定量成像技术在设计针对分子靶向、个性化治疗的肿瘤学试验中将发挥越来越重要的作用。分子靶向治疗的出现,以抗血管生成药物为例,在评估反应方面带来了新的复杂性。定量成像网络满足了对成像方式的需求,这些方式不仅可以准确和可重复地测量肿瘤大小的变化,还可以测量相关代谢参数的变化、相关信号通路的调节、药物向肿瘤的输送以及细胞凋亡死亡与肿瘤体积其他变化的区分。本文概述了定量成像在 0 期至 3 期肿瘤学试验中的应用。我们描述了一系列定量成像方式在特定肿瘤类型中的应用,包括恶性胶质瘤、肺癌、头颈部癌、淋巴瘤、乳腺癌、前列腺癌和肉瘤。在结论部分,我们讨论了使用定量成像进行临床试验的潜在限制,包括试验实施的复杂性、对受试者招募的影响、增量成本和机构障碍。还提出了克服这些限制的策略。