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Head-to-Head Comparison of SSTR Antagonist 68GaGa-DATA5m-LM4 with SSTR Agonist 68GaGa-DOTANOC PET/CT in Patients with Well Differentiated Gastroenteropancreatic Neuroendocrine Tumors: A Prospective Imaging Study
by
Yadav, Madhav P.
, Viswanathan, Rahul
, Ballal, Sanjana
, Satapathy, Swayamjeet
, Agarwal, Shipra
, Tripathi, Madhavi
, Moon, Euy Sung
, Roesch, Frank
, Bal, Chandrasekhar
, Sheokand, Parvind
in
[68Ga]Ga-DATA5m-LM4
/ [68Ga]Ga-DOTANOC
/ Biodistribution
/ Kidneys
/ Ligands
/ Lymphatic system
/ Medical imaging
/ Metastasis
/ NETs
/ Neuroendocrine tumors
/ Patients
/ PET/CT
/ SSTR antagonist
2024
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Head-to-Head Comparison of SSTR Antagonist 68GaGa-DATA5m-LM4 with SSTR Agonist 68GaGa-DOTANOC PET/CT in Patients with Well Differentiated Gastroenteropancreatic Neuroendocrine Tumors: A Prospective Imaging Study
by
Yadav, Madhav P.
, Viswanathan, Rahul
, Ballal, Sanjana
, Satapathy, Swayamjeet
, Agarwal, Shipra
, Tripathi, Madhavi
, Moon, Euy Sung
, Roesch, Frank
, Bal, Chandrasekhar
, Sheokand, Parvind
in
[68Ga]Ga-DATA5m-LM4
/ [68Ga]Ga-DOTANOC
/ Biodistribution
/ Kidneys
/ Ligands
/ Lymphatic system
/ Medical imaging
/ Metastasis
/ NETs
/ Neuroendocrine tumors
/ Patients
/ PET/CT
/ SSTR antagonist
2024
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Head-to-Head Comparison of SSTR Antagonist 68GaGa-DATA5m-LM4 with SSTR Agonist 68GaGa-DOTANOC PET/CT in Patients with Well Differentiated Gastroenteropancreatic Neuroendocrine Tumors: A Prospective Imaging Study
by
Yadav, Madhav P.
, Viswanathan, Rahul
, Ballal, Sanjana
, Satapathy, Swayamjeet
, Agarwal, Shipra
, Tripathi, Madhavi
, Moon, Euy Sung
, Roesch, Frank
, Bal, Chandrasekhar
, Sheokand, Parvind
in
[68Ga]Ga-DATA5m-LM4
/ [68Ga]Ga-DOTANOC
/ Biodistribution
/ Kidneys
/ Ligands
/ Lymphatic system
/ Medical imaging
/ Metastasis
/ NETs
/ Neuroendocrine tumors
/ Patients
/ PET/CT
/ SSTR antagonist
2024
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Head-to-Head Comparison of SSTR Antagonist 68GaGa-DATA5m-LM4 with SSTR Agonist 68GaGa-DOTANOC PET/CT in Patients with Well Differentiated Gastroenteropancreatic Neuroendocrine Tumors: A Prospective Imaging Study
Journal Article
Head-to-Head Comparison of SSTR Antagonist 68GaGa-DATA5m-LM4 with SSTR Agonist 68GaGa-DOTANOC PET/CT in Patients with Well Differentiated Gastroenteropancreatic Neuroendocrine Tumors: A Prospective Imaging Study
2024
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Overview
Neuroendocrine tumors (NETs) are slow-growing tumors that express high levels of somatostatin receptors (SSTRs). Recent studies have shown the superiority of radiolabeled SSTR antagonists in theranostics compared to agonists. In this prospective study, we compared the diagnostic efficacy between [68Ga]Ga-DOTANOC and [68Ga]Ga-DATA5m-LM4 in the detection of primary and metastatic lesions in patients with well differentiated gastroenteropancreatic (GEP) NETs. Histologically proven GEP-NET patients underwent [68Ga]Ga-DOTANOC & [68Ga]Ga-DATA5m-LM4 PET/CT scans, which were analyzed. The qualitative analysis involved the visual judgment of radiotracer uptake validated by the morphological findings using CT, which was considered as the reference standard. Quantitative comparisons were presented as the standardized uptake value (SUV) corrected for lean body mass: SULpeak, SULavg, and tumor-to-background ratios (TBR). In total, 490 lesions were confirmed via diagnostic CT. The lesion-based sensitivity of [68Ga]Ga-DATA5m-LM4 PET/CT was 94.28% (462/490) and 83.46% (409/490) for [68Ga]Ga-DOTANOC PET/CT (p < 0.0001). [68Ga]Ga-DATA5m-LM4 had statistical significance over [68Ga]Ga-DOTANOC in liver metastases [100% vs. 89.4%; p < 0.0001 (292 vs. 253 283 lesions on CT)] and bone metastases [100% vs. 82.9%; p = 0.005 (45 vs. 34 41 lesions on CT)]. Statistical significance was also noted for the TBR SULpeak of the primary and liver lesions. [68Ga]Ga-DATA5m-LM4 showed better sensitivity and a higher target-to-background ratio than [68Ga]Ga-DOTANOC PET/CT. [68Ga]Ga-DATA5m-LM4 PET/CT can be used to quantify the extent of skeletal and liver metastases for better planning of SSTR agonist- or antagonist-based therapy.
Publisher
MDPI AG,MDPI
Subject
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