Comparison of the Impact of 68Ga-DOTATATE and 18F-FDG PET/CT on Clinical Management in Patients with Neuroendocrine Tumors.

Panagiotidis, Emmanouil; Alshammari, Alshaima; Michopoulou, Sofia; Skoura, Evangelia; Naik, Keval; Maragkoudakis, Emmanouil; Mohmaduvesh, Mullan; Al-Harbi, Mohammed et al. · J Nucl Med · 2017

retrospective_cohort · Level III

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Abstract

This study aimed to assess the clinical impact of <sup>68</sup>Ga-DOTATATE and <sup>18</sup>F-FDG with respect to the management plan and to evaluate the prognostic value of both tracers. A total of 104 patients (55 male and 49 female; median age, 58 y; range, 20-90 y) with histologically proven neuroendocrine tumors (NETs) underwent both <sup>68</sup>Ga-DOTATATE and <sup>18</sup>F-FDG PET/CT. Twenty-eight patients (26.9%) had poorly differentiated tumors, and 76 (73.1%) had well-differentiated tumors. PET/CT results and SUVs were compared with prognostic factors such as histologic grade (G1, G2, or G3, for low-grade [well differentiated], intermediate-grade [moderately differentiated], and high-grade [poorly differentiated], respectively), chromogranin A, and proliferation index (Ki-67). The <sup>68</sup>Ga-DOTATATE and <sup>18</sup>F-FDG PET/CT findings were discordant in 65 patients (62.5%) and concordant in 39 patients (37.5%). The results changed the therapeutic plan in 84 patients (80.8%). In 22 patients (21.1%), decision making was based on the <sup>18</sup>F-FDG findings; in 32 (30.8%), on the findings with both radiotracers; and in 50 (48.1%), on the <sup>68</sup>Ga-DOTATATE findings. The most frequent management decision based on <sup>18</sup>F-FDG was initiation of chemotherapy (10 patients, 47.6%). The most common treatment decision due to <sup>68</sup>Ga-DOTATATE was initiation of peptide receptor radionuclide therapy (14 patients, 27.4%). In 11 (39.2%) of 28 patients with poorly differentiated NETs, the management decision was based on only the <sup>18</sup>F-FDG results. For <sup>68</sup>Ga-DOTATATE, SUV<sub>max</sub> was higher for G1 tumors and lower for G3 tumors (P = 0.012). However, no significant differences in <sup>18</sup>F-FDG-derived SUVs were observed between different grades (P = 0.38). The Mann-Whitney test showed significant differences in <sup>68</sup>Ga-DOTATATE SUV<sub>max</sub> between tumors with a Ki-67 of less than 5% and tumors with a Ki-67 of more than 5% (P = 0.004), without significance differences in <sup>18</sup>F-FDG SUV<sub>max</sub> Log-rank analysis showed statistically significant differences in survival for patients with bone metastasis versus soft-tissue or no metastasis for both <sup>18</sup>F-FDG (P = 0.037) and <sup>68</sup>Ga-DOTATATE (P = 0.047). Overall survival declined rapidly with increasing grade (P = 0.001), at an estimated 91 mo for G1, 59 mo for G2, and 48 mo for G3. <sup>18</sup>F-FDG PET/CT had no clinical impact on G1 NETs and a moderate impact on G2 NETs. However, in poorly differentiated NETs, <sup>18</sup>F-FDG PET/CT plays a significant clinical role in combination with <sup>68</sup>Ga-DOTATATE. <sup>68</sup>Ga DOTATATE SUV<sub>max</sub> relates to grade and Ki-67 and can be used prognostically.

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