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. 2021 Mar;35(3):281-290.
doi: 10.1007/s12149-021-01580-0. Epub 2021 Jan 31.

[18F]FDG PET/MRI in rectal cancer

Affiliations

[18F]FDG PET/MRI in rectal cancer

Filippo Crimì et al. Ann Nucl Med. 2021 Mar.

Abstract

We conducted a systematic literature review on the use of [18F]FDG PET/MRI for staging/restaging rectal cancer patients with PubMed, Scopus, and Web of Science, based on the PRISMA criteria. Three authors screened all titles and abstracts and examined the full texts of all the identified relevant articles. Studies containing aggregated or duplicated data, review articles, case reports, editorials, and letters were excluded. Ten reports met the inclusion criteria. Four studies examined T staging and one focused on local recurrences after surgery; the reported sensitivity (94-100%), specificity (73-94%), and accuracy (92-100%) varied only slightly from one study to another. The sensitivity, specificity, and accuracy of [18F]FDG PET/MRI for N staging were 90-93%, 92-94%, and 42-92%. [18F]FDG PET/MRI detected malignant nodes better than MRI, resulting in treatment change. For M staging, [18F]FDG PET/MRI outperformed [18F]FDG PET/CT and CT in detecting liver metastases, whereas it performed worse for lung metastases. The results of this review suggest that [18F]FDG PET/MRI should be used for rectal cancer restaging after chemoradiotherapy and to select patients for rectum-sparing approaches thanks to its accuracy in T and N staging. For M staging, it should be associated at least with a chest CT scan to rule out lung metastases.

Keywords: PET/MRI; Rectal cancer; [18F]FDG.

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Conflict of interest statement

The authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
The literature review flowchart
Fig. 2
Fig. 2
PET/MR images of a histologically-proven T2 rectal cancer after pCRT. a T2-weighted paraxial image showing an irregular thickening of the right rectal wall (arrow), with no signs of extramural invasion; b paraxial contrast-enhanced volumetric interpolated breath-hold examination (VIBE) with irregular enhancement of the same lesion (arrow); c axial b1000 diffusion-weighted imaging (DWI) showing signal restriction of the mass (arrow); d paraxial PET/MR fused image with hypermetabolism of the rectal tumour (arrow)
Fig. 3
Fig. 3
PET/MR images of a malignant mesorectal lymph node after pCRT. a T2-weighted paracoronal image showing rounded lymph node with short axis of 6 mm, irregular margins and internal signal heterogeneity (arrow); b paracoronal contrast-enhanced VIBE showing the same lymph node (arrow) with internal signs of necrosis; c axial b1000 diffusion-weighted imaging (DWI) identifying the lymph node (arrow); d paracoronal PET/MR fused image with slight hypermetabolism of the small lymph node (arrow)
Fig. 4
Fig. 4
PET/MR images of a small liver metastasis. a T2-weighted axial image showing small area of slight hyperintensity in S8 (arrow); b axial VIBE with a small hypointense lesion of 7 mm in S8 (arrow); c axial b1000 diffusion-weighted imaging (DWI) confirming the signal restriction of the mass (arrow); d axial PET/MR fused image with hypermetabolism of the liver lesion (arrow)

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