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The Combined Interpretation of 68Ga-DOTATATE PET/CT and 18F-FDG PET/CT in Metastatic Gastroenteropancreatic Neuroendocrine Tumors: A Classification System With Prognostic Impact.
Hayes, Aimee R; Furtado O'Mahony, Luke; Quigley, Ann-Marie; Gnanasegaran, Gopinath; Caplin, Martyn E; Navalkissoor, Shaunak; Toumpanakis, Christos.
Afiliación
  • Hayes AR; From the Neuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital.
  • Furtado O'Mahony L; Medical School, University College London.
  • Caplin ME; From the Neuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital.
  • Toumpanakis C; From the Neuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital.
Clin Nucl Med ; 47(1): 26-35, 2022 Jan 01.
Article en En | MEDLINE | ID: mdl-34874347
ABSTRACT

PURPOSE:

Gastroenteropancreatic neuroendocrine neoplasms (GEP NEN) are widely heterogeneous in their biological behavior, and predicting prognosis and optimal treatment strategies can be challenging. 68Ga-DOTATATE PET/CT is a sensitive imaging modality for well-differentiated NEN and indicates a favorable prognosis, whereas 18F-FDG PET/CT avidity indicates disease that is potentially more aggressive. There has been emerging interest in the combined interpretation of 68Ga-DOTATATE and 18F-FDG PET and its prognostic significance. We aimed to assess the prognostic utility of a classification system that incorporates the complex findings of 68Ga-DOTATATE and 18F-FDG PET interpreted side-by-side in patients with metastatic GEP NEN.

METHODS:

We defined 3 68Ga-DOTATATE/18F-FDG "dual-tracer PET" groups D1 (68Ga-DOTATATE positive/18F-FDG negative), D2 (68Ga-DOTATATE positive/18F-FDG positive), and D3 (68Ga-DOTATATE negative/18F-FDG positive). We retrospectively assessed the association between the dual-tracer PET classification and progression-free and overall survival (OS) using Kaplan-Meier analysis. Univariate and multivariate analyses were performed using the Cox proportional hazards model.

RESULTS:

Eighty-seven patients with metastatic GEP NEN and contemporaneous 68Ga-DOTATATE and 18F-FDG PET were included. The dual-tracer PET classification was an independent predictor of OS (multivariate P = 0.016) and also predicted progression-free survival (univariate P = 0.030). Other independent predictors of OS included chromogranin A and World Health Organization (WHO) grade. WHO grade was not associated with OS from the time of dual-tracer PET but was an independent predictor of OS from the date of histological diagnosis (multivariate P = 0.003).

CONCLUSION:

Our study demonstrates that a classification system combining the complex findings of 68Ga-DOTATATE and 18F-FDG PET is correlated with prognosis. Further research is needed to prospectively validate these findings and to explore whether dual-tracer PET scores may also be able to predict response to treatment.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Asunto principal: Compuestos Organometálicos / Tumores Neuroendocrinos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Nucl Med Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Asunto principal: Compuestos Organometálicos / Tumores Neuroendocrinos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Nucl Med Año: 2022 Tipo del documento: Article