Wang Weichen, Huang Mingxing, Tian Rong, Shen Guohua
Department of Nuclear Medicine, West China Hospital, Sichuan University, 37 Guoxue Alley, Chengdu 610041, Sichuan, China.
AJR Am J Roentgenol. 2025 Aug;225(2):e2532708. doi: 10.2214/AJR.25.32708. Epub 2025 May 14.
. Numerous studies have shown the superiority of PET/CT performed with the use of chemokine-targeted tracer Ga-boclatixafortide (Ga-PentixaFor, Pentixapharm) compared with FDG PET/CT for oncologic evaluation, although outcomes have varied across tumor types. . This study aimed to conduct a head-to-head comparison of Ga-PentixaFor PET/CT and FDG PET/CT for detecting hematologic malignancies and solid tumors. . The PubMed and Embase databases were searched through March 4, 2024, for studies reporting a head-to-head comparison of the detection performance of Ga-PentixaFor PET/CT versus FDG PET/CT in patients with cancer. Data were extracted from studies on a patient basis for each test in terms of the detection rate, SUV, and target-to-background ratio (TBR). The two tests were compared separately for hematologic malignancies and solid tumors. . The meta-analysis included 28 studies (15 studies of hematologic malignancies and 13 of solid cancers), with a total of 493 patients who underwent both tests. For hematologic malignancies, Ga-PentixaFor PET/CT, compared with FDG PET/CT, showed a significantly higher detection rate overall (relative risk [RR] = 1.19, < .001) and for bone marrow involvement (RR = 1.69, < .001), but it showed no significant difference for extramedullary involvement (RR = 1.10, = .88); Ga-PentixaFor PET/CT, compared with FDG PET/CT, showed a significantly higher SUV overall (mean difference [MD] = 2.26, < .001) for bone marrow involvement (MD = 4.75, < .001) and for extramedullary involvement (MD = 5.88, < .001), as well as a significantly higher TBR (MD = 1.28, = .03). For solid tumors, Ga-PentixaFor PET/CT, compared with FDG PET/CT, showed a significantly lower detection rate overall (RR = 0.73, = .005) but no significant difference for primary lesions (RR = 0.83, = .11), lymph node metastases (RR = 0.86, = .04), or distant metastases (RR = 0.64, = .13); Ga-PentixaFor PET/CT, compared with FDG PET/CT, showed a significantly lower SUV (MD = -8.79, < .001) and TBR (MD = -3.35, < .001). . In a head-to-head comparison of diagnostic performance, Ga-PentixaFor PET/CT outperformed FDG PET/CT for hematologic malignancies, whereas FDG PET/CT outperformed Ga-PentixaFor PET/CT for solid tumors. . The findings of this study can help guide the selection of optimal imaging strategies in patients with cancer.
多项研究表明,与氟代脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG PET/CT)相比,使用趋化因子靶向示踪剂镓-博克拉替沙肽(镓-喷替沙福,Pentixapharm)进行的PET/CT在肿瘤评估方面具有优势,尽管不同肿瘤类型的结果有所不同。本研究旨在对镓-喷替沙福PET/CT和FDG PET/CT在检测血液系统恶性肿瘤和实体瘤方面进行直接比较。通过检索截至2024年3月4日的PubMed和Embase数据库,查找报告镓-喷替沙福PET/CT与FDG PET/CT在癌症患者中检测性能直接比较的研究。从各项研究中按患者提取每次检查的检测率、标准化摄取值(SUV)和靶本比(TBR)数据。分别对血液系统恶性肿瘤和实体瘤进行两种检查的比较。荟萃分析纳入了28项研究(15项血液系统恶性肿瘤研究和13项实体癌研究),共有493例患者接受了两种检查。对于血液系统恶性肿瘤,与FDG PET/CT相比,镓-喷替沙福PET/CT总体检测率显著更高(相对危险度[RR]=1.19,P<.001),骨髓受累检测率也显著更高(RR=1.69,P<.001),但髓外受累方面无显著差异(RR=1.10,P=.88);与FDG PET/CT相比,镓-喷替沙福PET/CT骨髓受累(平均差值[MD]=4.75,P<.001)和髓外受累(MD=5.88,P<.001)的SUV总体显著更高,TBR也显著更高(MD=1.28,P=.03)。对于实体瘤,与FDG PET/CT相比,镓-喷替沙福PET/CT总体检测率显著更低(RR=0.73,P=.005),但原发灶(RR=0.83,P=.11)、淋巴结转移(RR=0.86,P=.04)或远处转移(RR=0.64,P=.13)方面无显著差异;与FDG PET/CT相比,镓-喷替沙福PET/CT的SUV(MD=-8.79,P<.001)和TBR(MD=-3.35,P<.001)显著更低。在诊断性能的直接比较中,镓-喷替沙福PET/CT在血液系统恶性肿瘤方面优于FDG PET/CT,而FDG PET/CT在实体瘤方面优于镓-喷替沙福PET/CT。本研究结果有助于指导癌症患者最佳成像策略的选择。