Tokac Recep Halit, Tokac Ekin Cemre Bayram, Yararbas Ulkem, Aykut Ayca, Durmaz Asude, Akin Haluk, Argon Aziz Murat
Department of Nuclear Medicine, Ege University Faculty of Medicine, Izmir, Turkey.
Department of Medical Genetics, Ege University Faculty of Medicine, Izmir, Turkey.
Cancer Med. 2025 Aug;14(16):e71049. doi: 10.1002/cam4.71049.
This study investigated the relationship between circulating tumor DNA (ctDNA) parameters and metabolic parameters from FDG PET/CT in advanced breast cancer (ABC) patients.
In this retrospective single-center study, 47 ABC patients who underwent both liquid biopsy and FDG PET/CT were analyzed.
Results showed that 27 patients (57.4%) had detectable ctDNA. Patients with detectable ctDNA demonstrated significantly higher whole-body metabolic tumor volume (WB-MTV) (p = 0.002) and whole-body total lesion glycolysis (WB-TLG) (p = 0.006) compared to those without ctDNA, while no significant difference was found in SUVmax or SUVmean. A moderate correlation was observed between variant allele frequency (VAF) values and metabolic parameters: maximum VAF correlated with SUVmax, WB-MTV, and WB-TLG (r = 0.407, p = 0.005; r = 0.457, p = 0.001; r = 0.415, p = 0.004, respectively). Mean VAF correlated with SUVmax, WB-MTV, and WB-TLG (r = 0.406, p = 0.005; r = 0.446, p = 0.002; r = 0.404, p = 0.005, respectively). The total VAF correlated with SUVmax, WB-MTV, and WB-TLG (r = 0.394, p = 0.006; r = 0.465, p = 0.001; r = 0.430, p = 0.003, respectively). When excluding patients without detectable ctDNA, the correlation between VAF values and WB-MTV, WB-TLG disappeared, while the correlation with SUVmax persisted. Total alteration number in ctDNA showed a moderate correlation with WB-MTV and WB-TLG (r = 0.563, p < 0.001; r = 0.459, p = 0.001, respectively). Correlation with WB-MTV remained significant when excluding patients without detectable ctDNA (r = 0.500, p = 0.008).
These findings suggest that metabolic tumor burden correlates with ctDNA detection and characteristics, potentially offering complementary information for disease monitoring, treatment selection, and response assessment in ABC. The combined use of these parameters may improve prognostic evaluation and guide personalized treatment strategies.
本研究调查了晚期乳腺癌(ABC)患者循环肿瘤DNA(ctDNA)参数与FDG PET/CT代谢参数之间的关系。
在这项回顾性单中心研究中,分析了47例同时接受液体活检和FDG PET/CT检查的ABC患者。
结果显示,27例患者(57.4%)可检测到ctDNA。与未检测到ctDNA的患者相比,检测到ctDNA的患者全身代谢肿瘤体积(WB-MTV)(p = 0.002)和全身总病变糖酵解(WB-TLG)(p = 0.006)显著更高,而SUVmax或SUVmean无显著差异。观察到变异等位基因频率(VAF)值与代谢参数之间存在中度相关性:最大VAF与SUVmax、WB-MTV和WB-TLG相关(r分别为0.407,p = 0.005;r = 0.457,p = 0.001;r = 0.415,p = 0.004)。平均VAF与SUVmax、WB-MTV和WB-TLG相关(r分别为0.406,p = 0.005;r = 0.446,p = 0.002;r = 0.404,p = 0.005)。总VAF与SUVmax、WB-MTV和WB-TLG相关(r分别为0.394,p = 0.006;r = 0.465,p = 0.001;r = 0.430,p = 0.003)。当排除未检测到ctDNA的患者时,VAF值与WB-MTV、WB-TLG之间的相关性消失,而与SUVmax的相关性仍然存在。ctDNA中的总改变数与WB-MTV和WB-TLG显示出中度相关性(r分别为0.563,p < 0.001;r = 0.459,p = 0.001)。排除未检测到ctDNA的患者后,与WB-MTV的相关性仍然显著(r = 0.500,p = 0.008)。
这些发现表明,代谢肿瘤负荷与ctDNA检测及特征相关,可能为ABC的疾病监测、治疗选择和反应评估提供补充信息。联合使用这些参数可能会改善预后评估并指导个性化治疗策略。