Chen Xiaoshan, Liu Yunuan, Zhao Xinming, Jing Fenglian, Wang Bin, Chen Xiaolin, Pang Xiao, Zhang Jingmian, Wang Jianfang, Zhang Zhaoqi, Han Jingya, Wang Mengjiao
Department of Nuclear Medicine, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Hebei Provincial Key Laboratory of Tumor Microenvironment and Drug Resistance, Shijiazhuang, China.
Cancer Biother Radiopharm. 2025 Mar;40(2):130-138. doi: 10.1089/cbr.2024.0182. Epub 2024 Oct 28.
We investigated the clinical practicability of same-day Ga-radiolabeled fibroblast activation protein inhibitors (Ga-FAPI)-first and F-fluorodeoxyglucose (F-FDG) imaging and compared it with same-day F-FDG-first or 2-day procedures in diagnosing gastrointestinal cancers. Sixty-five patients with confirmed gastrointestinal cancers were divided into same-day Ga-FAPI-first group (Group A), same-day F-FDG-first group (Group B), and 2-day group (Group C). Low-dose CT and low injection activity were performed on Ga-FAPI positron emission tomography/computed tomography (PET/CT). Interval times, radiation dose, diagnostic performance, and detectability were assessed among groups. Additionally, the uptake, tumor-to-liver ratio (TLR), diagnostic efficacy, and TNM stage were compared between the two modalities. The total waiting time for Group C was significantly longer than that for Group A or B (both < 0.001). The total dose-length product and effective dose decreased in all groups. There were comparable detectability and diagnostic performance among groups (all > 0.05). The within-group analysis in Group B indicated that Ga-FAPI PET/CT had higher uptake in the primary and recurrent lesions than F-FDG without differences in TLR, due to higher liver background on Ga-FAPI PET than Group A or C (both < 0.001).Ga-FAPI PET/CT possessed higher accuracy than F-FDG and changed staging in 14 patients (14/65, 21.54%). The same-day Ga-FAPI-first and F-FDG imaging reduced examination waiting time without increased radiation dose, simultaneously achieving excellent diagnostic performance and improving clinical staging in diagnosing gastrointestinal cancers.
我们研究了同一天进行镓(Ga)标记的成纤维细胞活化蛋白抑制剂(Ga-FAPI)先行和氟代脱氧葡萄糖(F-FDG)成像的临床实用性,并将其与同一天F-FDG先行或两天程序在诊断胃肠道癌症方面进行了比较。65例确诊为胃肠道癌症的患者被分为同一天Ga-FAPI先行组(A组)、同一天F-FDG先行组(B组)和两天程序组(C组)。对Ga-FAPI正电子发射断层扫描/计算机断层扫描(PET/CT)进行低剂量CT和低注射活度操作。评估各组之间的间隔时间、辐射剂量、诊断性能和可检测性。此外,还比较了两种模式之间的摄取、肿瘤与肝脏比值(TLR)、诊断效能和TNM分期。C组的总等待时间明显长于A组或B组(均P<0.001)。所有组的总剂量长度乘积和有效剂量均降低。各组之间的可检测性和诊断性能相当(均P>0.05)。B组的组内分析表明,由于Ga-FAPI PET上的肝脏背景高于A组或C组(均P<0.001),Ga-FAPI PET/CT在原发性和复发性病变中的摄取高于F-FDG,TLR无差异。Ga-FAPI PET/CT比F-FDG具有更高的准确性,并使14例患者(14/65,21.54%)的分期发生了改变。同一天Ga-FAPI先行和F-FDG成像减少了检查等待时间,且未增加辐射剂量,同时在诊断胃肠道癌症方面实现了优异的诊断性能并改善了临床分期。