Yahyanejad Sanaz, van Hoof Stefan J, Theys Jan, Barbeau Lydie M O, Granton Patrick V, Paesmans Kim, Verhaegen Frank, Vooijs Marc
Department of Radiotherapy (MAASTRO)/GROW - School for Developmental Biology & Oncology, Maastricht University, The Netherlands.
Department of Oncology, London Health Sciences Center, Canada.
Radiother Oncol. 2015 Sep;116(3):467-72. doi: 10.1016/j.radonc.2015.06.020. Epub 2015 Jul 7.
Glioblastoma multiforme is the most common malignant brain tumor. Standard treatment including surgery, radiotherapy and chemotherapy with temozolomide is not curative. There is a great need for in vitro and in vivo models closely mimicking clinical practice to ensure better translation of novel preclinical findings.
A 3D spheroid model was established using the U87MG cell line. The efficacy of temozolomide, RT and combinations was assessed using growth delay assays. Orthotopic glioblastoma tumors were established, different radiation doses delivered based on micro-CT based treatment planning (SmART-plan) and dose volume histograms (DVH) were determined. Tumor growth was monitored using bioluminescent imaging.
3D spheroid cultures showed a dose-dependent growth delay upon single and combination treatments. Precise uniform radiation was achieved in all in vivo treatment groups at all doses tested, and DVHs showed accurate dose coverage in the planning target volume which resulted in tumor growth delay.
We demonstrate that 3D spheroid technology can be reliably used for treatment efficacy evaluation and that mimicking a clinical setting is also possible in small animals. Both these in vitro and in vivo techniques can be combined for clinically relevant testing of novel drugs combined with radiation.
多形性胶质母细胞瘤是最常见的恶性脑肿瘤。包括手术、放疗及替莫唑胺化疗在内的标准治疗无法治愈该病。迫切需要能紧密模拟临床实践的体外和体内模型,以确保更好地转化新的临床前研究结果。
使用U87MG细胞系建立3D球体模型。通过生长延迟试验评估替莫唑胺、放疗及联合治疗的疗效。建立原位胶质母细胞瘤肿瘤模型,基于微型计算机断层扫描(micro-CT)的治疗计划(智能计划)给予不同辐射剂量,并确定剂量体积直方图(DVH)。使用生物发光成像监测肿瘤生长。
3D球体培养在单一治疗及联合治疗后均显示出剂量依赖性生长延迟。在所有测试剂量下,所有体内治疗组均实现了精确均匀的辐射,且DVH显示在计划靶体积中有准确的剂量覆盖,这导致了肿瘤生长延迟。
我们证明3D球体技术可可靠地用于治疗疗效评估,并且在小动物中模拟临床环境也是可行的。这两种体外和体内技术可结合用于新药联合放疗的临床相关测试。