Corroyer-Dulmont Aurélien, Pérès Elodie A, Gérault Aurélie N, Savina Ariel, Bouquet Fanny, Divoux Didier, Toutain Jérôme, Ibazizène Méziane, MacKenzie Eric T, Barré Louisa, Bernaudin Myriam, Petit Edwige, Valable Samuel
CNRS, UMR 6301 ISTCT, CERVOxy and LDM-TEP groups. GIP CYCERON, Bd H Becquerel, BP 5229, 14074, Caen Cedex, France.
CEA, DSV/I2BM, UMR 6301 ISTCT, CERVOxy and LDM-TEP groups. GIP CYCERON, Bd Henri Becquerel, BP 5229, 14074, Caen Cedex, France.
Eur J Nucl Med Mol Imaging. 2016 Apr;43(4):682-94. doi: 10.1007/s00259-015-3225-0. Epub 2015 Nov 5.
The primary objective of this study was to compare the ability of PET and MRI biomarkers to predict treatment efficacy in a preclinical model of recurrent glioblastoma multiforme.
MRI (anatomical, diffusion, vasculature and oxygenation) and PET ([(18)F]FDG and [(18)F]FLT) parameters were obtained 3 days after the end of treatment and compared with late tumour growth and survival.
Early after tumour recurrence, no effect of treatment with temozolomide combined with bevacizumab was observed on tumour volume as assessed by T2-W MRI. At later times, the treatment decreased tumour volume and increased survival. Interestingly, at the earlier time, temozolomide + bevacizumab decreased [(18)F]FLT uptake, cerebral blood volume and oedema. [(18)F]FLT uptake, oedema and cerebral blood volume were correlated with overall survival but [(18)F]FLT uptake had the highest specificity and sensitivity for the early prediction of treatment efficacy.
The present investigation in a preclinical model of glioblastoma recurrence underscores the importance of multimodal imaging in the assessment of oedema, tumour vascular status and cell proliferation. Finally, [(18)F]FLT holds the greatest promise for the early assessment of treatment efficacy. These findings may translate clinically in that individualized treatment for recurrent glioma could be prescribed for patients selected after PET/MRI examinations.
本研究的主要目的是比较PET和MRI生物标志物在多形性胶质母细胞瘤复发临床前模型中预测治疗效果的能力。
在治疗结束后3天获得MRI(解剖、扩散、血管和氧合)及PET([(18)F]FDG和[(18)F]FLT)参数,并与肿瘤晚期生长和生存期进行比较。
肿瘤复发早期,通过T2加权MRI评估,未观察到替莫唑胺联合贝伐单抗治疗对肿瘤体积有影响。在后期,该治疗减小了肿瘤体积并延长了生存期。有趣的是,在早期,替莫唑胺+贝伐单抗降低了[(18)F]FLT摄取、脑血容量和水肿。[(18)F]FLT摄取、水肿和脑血容量与总生存期相关,但[(18)F]FLT摄取对治疗效果的早期预测具有最高的特异性和敏感性。
目前在胶质母细胞瘤复发临床前模型中的研究强调了多模态成像在评估水肿、肿瘤血管状态和细胞增殖方面的重要性。最后,[(18)F]FLT在治疗效果的早期评估方面最具前景。这些发现可能具有临床意义,即对于经PET/MRI检查后选定的患者,可以开出复发性胶质瘤的个体化治疗方案。