Supiot Stéphane, Rousseau Caroline, Dore Mélanie, Cheze-Le-Rest Catherine, Kandel-Aznar Christine, Potiron Vincent, Guerif Stéphane, Paris François, Ferrer Ludovic, Campion Loïc, Meingan Philippe, Delpon Gregory, Hatt Mathieu, Visvikis Dimitris
Institut de Cancérologie de l'Ouest, Bld Jacques Monod, 44805 Nantes-Saint Herblain, France.
Centre de Recherche en Cancérologie Immunologie Nantes/Angers (CRCNA, UMR 1232 INSERM), Institut de Recherche en Santé de l'Université de Nantes, 44007 Nantes CEDEX 1, France.
Oncotarget. 2018 Jan 13;9(11):10005-10015. doi: 10.18632/oncotarget.24234. eCollection 2018 Feb 9.
Hypoxia is a major factor in prostate cancer aggressiveness and radioresistance. Predicting which patients might be bad candidates for radiotherapy may help better personalize treatment decisions in intermediate-risk prostate cancer patients. We assessed spatial distribution of F-Misonidazole (FMISO) PET/CT uptake in the prostate prior to radiotherapy treatment.
Intermediate-risk prostate cancer patients about to receive high-dose (>74 Gy) radiotherapy to the prostate without hormonal treatment were prospectively recruited between 9/2012 and 10/2014. Prior to radiotherapy, all patients underwent a FMISO PET/CT as well as a MRI and F-choline-PET. F-choline and FMISO-positive volumes were semi-automatically determined using the fuzzy locally adaptive Bayesian (FLAB) method. In FMISO-positive patients, a dynamic analysis of early tumor uptake was performed. Group differences were assessed using the Wilcoxon signed rank test. Parameters were correlated using Spearman rank correlation.
Of 27 patients (median age 76) recruited to the study, 7 and 9 patients were considered positive at 2.5h and 3.5h FMISO PET/CT respectively. Median SUV and SUV tumor to muscle (T/M) ratio were respectively 3.4 and 3.6 at 2.5h, and 3.2 and 4.4 at 3.5h. The median FMISO-positive volume was 1.1 ml.
This is the first study regarding hypoxia imaging using FMISO in prostate cancer showing that a small FMISO-positive volume was detected in one third of intermediate-risk prostate cancer patients.
缺氧是前列腺癌侵袭性和放射抗性的主要因素。预测哪些患者可能不适合放疗,有助于更好地为中危前列腺癌患者制定个性化治疗决策。我们评估了放疗前前列腺中F-米索硝唑(FMISO)PET/CT摄取的空间分布。
2012年9月至2014年10月前瞻性招募了即将接受前列腺高剂量(>74 Gy)放疗且未接受激素治疗的中危前列腺癌患者。放疗前,所有患者均接受了FMISO PET/CT、MRI和F-胆碱PET检查。使用模糊局部自适应贝叶斯(FLAB)方法半自动确定F-胆碱和FMISO阳性体积。对FMISO阳性患者进行早期肿瘤摄取的动态分析。使用Wilcoxon符号秩检验评估组间差异。使用Spearman秩相关分析参数之间的相关性。
纳入该研究的27例患者(中位年龄76岁)中,分别有7例和9例在FMISO PET/CT检查2.5小时和3.5小时时被认为呈阳性。2.5小时时的SUV中位数和肿瘤与肌肉(T/M)SUV比值分别为3.4和3.6,3.5小时时分别为3.2和4.4。FMISO阳性体积中位数为1.1 ml。
这是第一项关于在前列腺癌中使用FMISO进行缺氧成像的研究,表明在三分之一的中危前列腺癌患者中检测到较小的FMISO阳性体积。