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Comparison of integrin αvβ3 expression with 68Ga-NODAGA-RGD PET/CT and glucose metabolism with 18F-FDG PET/CT in esophageal or gastroesophageal junction cancers
Background The primary aims of this study were to compare in patients with esophageal or esophagogastric junction cancers the potential of 68 Ga-NODAGA-RGD PET/CT with that of 18 F-FDG PET/CT regarding tumoral uptake and distribution, as well as histopathologic examination. Methods Ten 68 Ga-NODAGA-...
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Published in: | European journal of hybrid imaging 2023-02, Vol.7 (1), p.3-3, Article 3 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Background
The primary aims of this study were to compare in patients with esophageal or esophagogastric junction cancers the potential of
68
Ga-NODAGA-RGD PET/CT with that of
18
F-FDG PET/CT regarding tumoral uptake and distribution, as well as histopathologic examination.
Methods
Ten
68
Ga-NODAGA-RGD and ten
18
F-FDG PET/CT were performed in nine prospectively included participants (1 woman; aged 58 ± 8.4 y, range 40–69 y). Maximum SUV (SUV
max
) and metabolic tumor volumes (MTV) were calculated. The Mann–Whitney U test and Spearman correlation analysis (
ρ
) were used.
Results
68
Ga-NODAGA-RGD PET/CT detected positive uptake in 10 primary sites (8 for primary tumors and 2 for local relapse suspicion), 6 lymph nodes and 3 skeletal sites.
18
F-FDG PET/CT detected positive uptake in the same sites but also in 16 additional lymph nodes and 1 adrenal gland. On a lesion-based analysis, SUV
max
of
18
F-FDG was significantly higher than those of
68
Ga-NODAGA-RGD (4.9 [3.7–11.3] vs. 3.2 [2.6–4.2] g/mL,
p
= 0.014). Only one participant showed a higher SUV
max
in an osseous metastasis with
68
Ga-NODAGA-RGD as compared to
18
F-FDG (6.6 vs. 3.9 g/mL). Correlation analysis showed positive correlation between
18
F-FDG and
68
Ga-NODAGA-RGD PET parameters (
ρ
= 0.56,
p
= 0.012 for SUV
max
,
ρ
= 0.78,
p
|
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ISSN: | 2510-3636 2510-3636 |
DOI: | 10.1186/s41824-023-00162-9 |