Cho Linda P, Kim Chun K, Viswanathan Akila N
Department of Radiation Oncology, Brigham and Women's Hospital, Boston, MA, United States; Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Brigham and Women's Hospital, Boston, MA, United States; Harvard Medical School, Boston, MA, United States.
Gynecol Oncol Rep. 2015 Nov 2;14:34-7. doi: 10.1016/j.gore.2015.10.003. eCollection 2015 Nov.
The role of F-18-fluorothymidine (FLT) PET-CT imaging in the evaluation of gynecologic cancers has not been established. We sought to evaluate (FLT) PET-CT imaging in gynecologic cancers by comparing standard uptake values (SUVs) of FLT with F-18-fluorodeoxyglucose (FDG) PET in the primary tumor at diagnosis, and assess FLT uptake immediately following concurrent chemoradiotherapy (chemoRT).
In this pilot study, patients treated for cervical (5) or vaginal (1) cancer underwent FLT-PET and FDG-PET scanning at diagnosis (FLT1 and FDG1). Five patients (4 cervical and 1 vaginal) also underwent FLT-PET within 1-3 weeks after chemoRT before brachytherapy (FLT2). Wilcoxon rank-sum test was used to compare the FLT1 and FDG1 parameters.
Median age at diagnosis was 61-years (range, 33-72). Cervical cancers were staged as IB2 (n = 1, 20%), IIB (n = 1, 20%), IIIB (n = 1, 20%) and IVA (n = 2, 40%) and the single vaginal cancer was staged IIIB. The most common histology was squamous cell carcinoma (n = 3, 50%) followed by adenocarcinoma (n = 2, 33%) and clear-cell adenosquamous carcinoma (n = 1, 17%). Median tumor SUVmax at diagnosis was 7.8 on FLT1-PET (3.9-14.2) versus 11.6 (5.9-23.2) on FDG1-PET (p = 0.15). Tumor SUVmax of FLT declined 54%-100% after chemoRT.
The tumor SUV of FLT at diagnosis was lower than that of FDG-PET. FLT uptake was markedly decreased after chemoRT. Results indicate that there may not be a significant effect of inflammation on FLT uptake in gynecologic cancers. FLT may be a useful tool when assessing the effects of chemoRT on gynecologic malignancies and planning for postchemoRT brachytherapy treatments.
18F-氟胸苷(FLT)PET-CT成像在妇科癌症评估中的作用尚未明确。我们试图通过比较诊断时原发性肿瘤中FLT的标准摄取值(SUV)与18F-氟脱氧葡萄糖(FDG)PET,来评估FLT PET-CT成像在妇科癌症中的应用,并评估同步放化疗(chemoRT)后立即进行的FLT摄取情况。
在这项前瞻性研究中,接受宫颈癌(5例)或阴道癌(1例)治疗的患者在诊断时接受了FLT-PET和FDG-PET扫描(FLT1和FDG1)。5例患者(4例宫颈癌和1例阴道癌)在chemoRT后1-3周内、近距离放疗前也接受了FLT-PET检查(FLT2)。采用Wilcoxon秩和检验比较FLT1和FDG1参数。
诊断时的中位年龄为61岁(范围33-72岁)。宫颈癌分期为IB2期(n = 1,20%)、IIB期(n = 1,20%)、IIIB期(n = 1,20%)和IVA期(n = 2,40%),单一阴道癌分期为IIIB期。最常见的组织学类型是鳞状细胞癌(n = 3,50%),其次是腺癌(n = 2,33%)和透明细胞腺鳞癌(n = 1,17%)。诊断时肿瘤的中位SUVmax在FLT1-PET上为7.8(3.9-14.2),而在FDG1-PET上为11.6(5.9-23.2)(p = 0.15)。chemoRT后FLT的肿瘤SUVmax下降了54%-100%。
诊断时FLT的肿瘤SUV低于FDG-PET。chemoRT后FLT摄取明显降低。结果表明,炎症对妇科癌症中FLT摄取可能没有显著影响。在评估chemoRT对妇科恶性肿瘤的疗效以及规划chemoRT后近距离放疗治疗时,FLT可能是一种有用的工具。