Author/Authors :
Zhang, Panpan Department of Gastrointestinal Oncology - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China , Yu, Jiangyuan Department of Nuclear Medicine - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China , Li, Jie Department of Gastrointestinal Oncology - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China , Shen, Lin Department of Gastrointestinal Oncology - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China , Li, Nan Department of Nuclear Medicine - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China , Zhu, Hua Department of Nuclear Medicine - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China , Zhai, Shizhen Department of Nuclear Medicine - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China , Zhang, Yan Department of Nuclear Medicine - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China , Yang, Zhi Department of Nuclear Medicine - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China , Lu, Ming Department of Gastrointestinal Oncology - Key Laboratory of Carcinogenesis and Translational Research - Ministry of Education - Peking University School of Oncology - Beijing Cancer Hospital and Institute - Beijing, China
Abstract :
To evaluate the clinical and prognostic value of PET/CT with combination of 68Ga-DOTATATE and 18F-FDG
in gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs). Method. 83 patients of GEP-NENs who underwent 68GaDOTATATE and 18F-FDG PET/CT were enrolled between June 2013 and December 2016. Well-diferentiated (WD) NETs are
divided into group A (Ki-67 < 10%) and group B (Ki-67 ≥ 10%), and poorly diferentiated (PD) NECs are defined as group
C. The relationship between PET/CT results and clinicopathological characteristics was retrospectively investigated. Result. For
groups A/B/C, the sensitivities of 68Ga-DOTATATE and 18F-FDG were 78.8%/83.3%/37.5% and 52.0%/72.2%/100.0%. A negative
correlation between Ki-67 and SUVmax of 68Ga-DOTATATE (R = −0.415; p ≤ 0.001) was observed, while a positive correlation was
noted between Ki-67 and SUVmax of 18F-FDG (R = 0.683; p ≤ 0.001). 62.5% (5/8) of patients showed signifcantly more lesions
in the bone if 68Ga-DOTATATE was used, and 22.7% (5/22) of patients showed more lymph node metastases if 18F-FDG was
used. Conclusions. The sensitivity of dual tracers was correlated with cell diferentiation, and a correlation between Ki-67 and both
SUVmax of PET-CTs could be observed. 68Ga-DOTATATE is suggested for WD-NET and 18F-FDG is probably suitable for patients
with Ki-67 ≥ 10%.
Keywords :
PET/CT , 18F-FDG , 68Ga-DOTATATE , GEP-NEN