Veenstra Emile B, Ruiter Simeon J S, de Haas Robbert J, de Jong Koert P, Erba Paola A, Dierckx Rudi A J O, Noordzij Walter
Department of Nuclear Medicine and Molecular Imaging, Medical Imaging Center, University of Groningen, University Medical Center Groningen, P.O. Box 30.001, 9700 RB, Groningen, The Netherlands.
Department of Hepato-Pancreato-Biliary Surgery and Liver Transplantation, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
EJNMMI Res. 2023 Aug 29;13(1):77. doi: 10.1186/s13550-023-01024-y.
Early detection of recurrent or progressive HCC remains the strongest prognostic factor for survival. Dual tracer PET/CT imaging with [C]CH and [F]FDG can further increase detection rates as both tracers entail different metabolic pathways involved in HCC development. We investigated dual-tracer PET/CT in clinical decision making in patients suspected of recurrent or progressive HCC. All HCC patients who underwent both [C]CH and [F]FDG PET/CT in our institute from February 2018 to December 2021 were included. Both tracer PET/CT were within 4 weeks of each other with at least 6-month follow-up. Patients underwent dual tracer PET/CT because of unexplained and suspicious CT/MRI or sudden rise of serum tumour markers. A detected lesion was considered critical when the finding had prognostic consequences leading to treatment changes.
Nineteen patients who underwent [C]CH and [F]FDG PET/CT were included of which all but six patients were previously treated for HCC. Dual-tracer critical finding detection rate was 95%, with [F]FDG 68%, and [C]CH 84%. Intrahepatic HCC recurrence finding rate was 65% for both tracers. [F]FDG found more ablation site recurrences (4/5) compared to [C]CH (2/5). Only [C]CH found two needle tract metastases. Both tracers found 75% of the positive lymph nodes. Two new primary tumours were found, one by [F]FDG and both by [C]CH.
Our study favours a dual-tracer approach in HCC staging in high-risk patients or when conventional imaging is non-conclusive.
复发性或进展性肝癌的早期检测仍然是生存的最强预后因素。采用[C]CH和[F]FDG的双示踪剂PET/CT成像可进一步提高检测率,因为这两种示踪剂涉及肝癌发展过程中不同的代谢途径。我们研究了双示踪剂PET/CT在疑似复发性或进展性肝癌患者临床决策中的应用。纳入了2018年2月至2021年12月在我院接受[C]CH和[F]FDG PET/CT检查的所有肝癌患者。两种示踪剂PET/CT检查间隔在4周内,且随访至少6个月。患者因无法解释的可疑CT/MRI或血清肿瘤标志物突然升高而接受双示踪剂PET/CT检查。当检测到的病变具有导致治疗改变的预后后果时,该病变被视为关键病变。
纳入了19例接受[C]CH和[F]FDG PET/CT检查的患者,其中除6例患者外,其余均曾接受过肝癌治疗。双示踪剂关键病变检测率为95%,[F]FDG为68%,[C]CH为84%。两种示踪剂对肝内肝癌复发的检出率均为65%。与[C]CH(2/5)相比,[F]FDG发现更多消融部位复发(4/5)。仅[C]CH发现两例针道转移。两种示踪剂均发现75%的阳性淋巴结。发现两例新发原发性肿瘤,一例由[F]FDG发现,两例均由[C]CH发现。
我们的研究支持在高危患者或传统成像结果不明确时采用双示踪剂方法进行肝癌分期。