Dagher Samir A, Johnson Jason M, Mohamed Rania M M, Ansari Shehbaz, Mawlawi Osama, Liu Ho-Ling, Wintermark Max, Schellingerhout Dawid, Flynt Lesley, Yeboa Debra N, Weinberg Jeffrey S, Ferguson Sherise D, Gule-Monroe Maria K
Department of Neuroradiology, The University of Texas MD Anderson Cancer Center, 1400 Pressler Street, Houston, TX, 77030, USA.
Department of Radiology and Biomedical Imaging, Yale University, New Haven, CT, USA.
J Neurooncol. 2025 Jul 1. doi: 10.1007/s11060-025-05146-2.
Recent evidence supports incorporating 18 F-Fluciclovine PET for glioblastoma treatment planning and monitoring, as it better captures tumor infiltration compared to conventional MRI. However, the relationship between PET- and MRI-defined tumor volumes remains unclear, particularly in the post-treatment setting. This study prospectively compares tumor volumes on MRI and PET at multiple timepoints throughout the treatment course and evaluates volumetric changes with therapy.
We prospectively enrolled 8 adults with IDH-wildtype glioblastoma treated with surgery and chemoradiation between September 2019 and 2021. Participants underwent paired 18 F-Fluciclovine PET/CT and conventional MRI at four timepoints: preoperatively, pre-radiation, and at one- and six-months post-radiation. Biological tumor volume (BTV) from PET, FLAIR, and post-contrast T1volumes (T1CV) were segmented. Volumetric changes were compared using the Friedman test.
Participants (5 males, median age 63 years [IQR 54,66]) showed significantly larger BTVs compared to T1CV at diagnosis (median BTV = 27.2mL vs. T1CV = 13.3mL, adjusted P =.03), pre-radiation (BTV = 25.2mL vs. T1CV = 6.9mL, adjusted P =.03), and at one-month post-radiation (BTV = 27.3mL vs. T1CV = 12.1mL, P =.04). BTVs closely approximated yet were slightly smaller than their corresponding FLAIR volumes at all timepoints. After surgery, the median decrease in BTV (-4.4%) was significantly smaller than T1CV (-66.5%, P =.046), with a similar nonsignificant trend observed post-radiation (P =.50).
Glioblastoma BTVs consistently exceed post-contrast T1 volumes and closely approximate FLAIR abnormalities throughout treatment. BTVs decline more gradually post-treatment, indicating persistent hypermetabolic tumor burden. Thus, 18 F-Fluciclovine PET can serve as an adjunct to conventional MRI in glioblastoma treatment planning and monitoring.
最近有证据支持将18F-氟代脱氧胸苷正电子发射断层扫描(18F-Fluciclovine PET)用于胶质母细胞瘤的治疗计划制定和监测,因为与传统磁共振成像(MRI)相比,它能更好地显示肿瘤浸润情况。然而,PET和MRI所定义的肿瘤体积之间的关系仍不明确,尤其是在治疗后的情况下。本研究前瞻性地比较了整个治疗过程中多个时间点的MRI和PET上的肿瘤体积,并评估了治疗引起的体积变化。
我们前瞻性地纳入了8例在2019年9月至2021年期间接受手术及放化疗的异柠檬酸脱氢酶(IDH)野生型胶质母细胞瘤成年患者。参与者在四个时间点接受了18F-氟代脱氧胸苷PET/CT和传统MRI检查:术前、放疗前、放疗后1个月和6个月。对PET、液体衰减反转恢复序列(FLAIR)和增强后T1加权像上的肿瘤体积(T1CV)进行分割。使用Friedman检验比较体积变化。
参与者(5名男性;中位年龄63岁[四分位间距54,66])在诊断时(中位BTV = 27.2mL vs. T1CV = 13.3mL,校正P = 0.03)、放疗前(BTV = 25.2mL vs. T1CV = 6.9mL,校正P = 0.03)和放疗后1个月(BTV = 27.3mL vs. T1CV = 12.1mL,P = 0.04)时,BTV均显著大于T1CV。在所有时间点,BTV均与相应的FLAIR体积相近但略小。手术后,BTV中位数下降幅度(-4.4%)显著小于T1CV(-66.5%,P = 0.046),放疗后也观察到类似的无显著差异趋势(P = 0.50)。
胶质母细胞瘤的BTV在整个治疗过程中始终超过增强后T1加权像上的体积,并与FLAIR异常情况相近。治疗后BTV下降更为缓慢,表明存在持续的高代谢肿瘤负荷。因此,18F-氟代脱氧胸苷PET可作为传统MRI的辅助手段用于胶质母细胞瘤的治疗计划制定和监测。