68Ga-DOTATATE PET/CT in the Initial Staging of Well-Differentiated Gastroenteropancreatic and Non-Gastroenteropancreatic Neuroendocrine Tumors: Results of a Prospective Registry
<b>Background and Objectives:</b> At diagnosis, the initial staging of well-differentiated neuroendocrine tumors (WD NETs) aids in treatment planning. The somatostatin receptor (SSTR)-PET has been recommended for staging of WD NETs although limited data are available on its impact on non-gastroeneteropancreatic (GEP) NETs. The main purpose of this study was to compare the stage migration after the addition of SSTR-PET to the workup of patients at the initial staging of GEP NETs to those with non-GEP NETs, and its potential impact on patient management. <b>Methods:</b> This prospective study included patients with WD NETs at initial staging. Demographic data, results of conventional and SSTR-PET staging, and SUVmax were recorded. Three panels of experts assessed the potential impact of SSTR-PET to management. <b>Results:</b> There were 482 patients, including 376 with gastroenteropancreatic (GEP) NETs and 106 non-GEP NETs with a median SUVmax of 34.7 [Q1, Q3: 22.8, 59.1]) and 19.0 [Q1, Q3: 7.9, 39.8]), respectively; <i>p</i> < 0.001. The discordant M-stage was recorded in 111/473 patients (23.5%). PET suggested a higher stage in 78/369 GEP NETs (21.1%), including the detection of extrahepatic metastatic disease in 42/114 (36.8%) patients with liver metastases only on CI. For non-GEP NETs, PET suggested a higher stage in 10/104 (9.6%) and CI suggested a higher stage in 15/104 (14.4%), with CI detecting liver metastases more frequently. The potential impact to management for patients with discordant M-stage was scored as moderate to high between 57/101 (56.4%) and 79/101 (78.2%) of patients. <b>Conclusions:</b> One in five patients are upstaged following SSTR-PET, more frequently with GEP NETs than others. SSTR-PET identifies extrahepatic metastatic disease in >1/3 of patients with presumed liver-only metastases on CI. Stage migration following SSTR-PET may result in frequent moderate or significant management change.
Authors
- Rebecca Wong (ORCID: https://orcid.org/0000-0001-7210-3330)
- Patrick Veit‐Haibach (ORCID: https://orcid.org/0000-0002-8607-2667)
- Ricarda Hinzpeter (ORCID: https://orcid.org/0000-0002-4707-3042)
- Amit Singnurkar (ORCID: https://orcid.org/0000-0002-1731-9507)
- Daryl Gray (ORCID: https://orcid.org/0000-0001-9773-4075)
- Roshini Kulanthaivelu (ORCID: https://orcid.org/0000-0002-2279-8346)
- Sten Myrehaug (ORCID: https://orcid.org/0000-0002-5765-1969)
- Ur Metser (ORCID: https://orcid.org/0000-0003-3726-8994)
- Julia Duder
- Shereen Ezzat
- Xuan Li (ORCID: https://orcid.org/0000-0001-5781-1662)
- Simron Singh (ORCID: https://orcid.org/0000-0002-5179-7043)
Institutions
- Western University (CA)
- Mount Sinai Hospital (CA)
- Sunnybrook Health Science Centre (CA)
- University Health Network (CA)
- University of Toronto (CA)
- London Health Sciences Centre (CA)
- Women's College Hospital (CA)
- Health Sciences Centre (CA)
- Princess Margaret Cancer Centre (CA)
- Victoria Hospital (CA)
Publication Details
- Journal
- Cancers
- Published
- 2025-01-27
- DOI
- https://doi.org/10.3390/cancers17030434
- Primary Topic
- Neuroendocrine Tumor Research Advances
- Type
- article
- Field-Weighted Citation Impact
- 0.00