Skip to main content
NCBI home page
Radiology and Oncology logoLink to Radiology and Oncology
. 2013 Jul 30;47(3):206–218. doi: 10.2478/raon-2013-0007

Comparison between whole-body MRI and Fluorine-18-Fluorodeoxyglucose PET or PET/CT in oncology: a systematic review

Mario Ciliberto 1,*, Fabio Maggi 1, Giorgio Treglia 2,*,✉, Federico Padovano 1, Lucio Calandriello 1, Alessandro Giordano 2, Lorenzo Bonomo 1
PMCID: PMC3794875  PMID: 24133384

Abstract

Background

The aim of the article is to systematically review published data about the comparison between positron emission tomography (PET) or PET/computed tomography (PET/CT) using Fluorine-18-Fluorodeoxyglucose (FDG) and whole-body magnetic resonance imaging (WB-MRI) in patients with different tumours.

Methods

A comprehensive literature search of studies published in PubMed/MEDLINE, Scopus and Embase databases through April 2012 and regarding the comparison between FDG-PET or PET/CT and WB-MRI in patients with various tumours was carried out.

Results

Forty-four articles comprising 2287 patients were retrieved in full-text version, included and discussed in this systematic review. Several articles evaluated mixed tumours with both diagnostic methods. Concerning the specific tumour types, more evidence exists for lymphomas, bone tumours, head and neck tumours and lung tumours, whereas there is less evidence for other tumour types.

Conclusions

Overall, based on the literature findings, WB-MRI seems to be a valid alternative method compared to PET/CT in oncology. Further larger prospective studies and in particular cost-effectiveness analysis comparing these two whole-body imaging techniques are needed to better assess the role of WB-MRI compared to FDG-PET or PET/CT in specific tumour types.

Keywords: positron emission tomography, PET/CT, fluorodeoxyglucose, whole-body magnetic resonance imaging, diffusion-weighted imaging, oncology

Introduction

Accurate staging and thorough tumour surveillance are essential in patients with a neoplastic disease to assess prognosis and to decide the most appropriate therapeutic options. Imaging plays a key role in these evaluation steps: multi-slice computed tomography (CT) and, recently, positron emission tomography/CT (PET/CT) are widely used in order to get an integrated diagnostic approach to cancer as a systemic disease.1 In particular, the use of Fluorine-18-Fluorodeoxyglucose (FDG) tracer made, up to now, PET contribution to oncologic imaging matchless by any other functional imaging modality.2 However, this technique uses ionizing radiations and has some limitations for what concerns spatial and contrast resolution; false positive and false negative results of FDG-PET are well known, too.

Magnetic resonance imaging (MRI), with its lack of ionizing radiation, high soft tissue contrast and good spatial resolution, is a useful application for tumour detection and staging of malignancies and could overcome the limits of FDG-PET/CT.3

In recent years, significant improvements in hardware and important innovations in sequence design and image acquisition have allowed a whole-body imaging with MRI in a suitable acquisition time without impairment of spatial resolution.4 Furthermore, the introduction of diffusion-weighted MRI (DWI) has increased the potential for the detection of malignancies throughout the body.5 Whole body MRI (WB-MRI) has then emerged as an excellent candidate for staging and surveillance of patients with neoplastic disease and many authors have compared FDG-PET/CT and WB-MRI in oncology.

Our article aims to systematically review the current evidence on the comparison between PET or PET/CT using FDG and WB-MRI in patients with different tumours.

Methods

A comprehensive literature search of studies published in PubMed/MEDLINE, Scopus and Embase databases was carried out to find relevant peer-reviewed articles on the comparison of FDG-PET or PET/CT and WB-MRI in patients with different tumours.

A search algorithm based on a combination of the terms: a) “PET” OR “positron emission tomography” AND b) “whole body MR” OR “whole-body MR” OR “whole body magnetic resonance” OR “whole-body magnetic resonance” OR “whole body MRI” OR “whole-body MRI” was used. No beginning date limit was used and the search was updated until April 2012.

All the studies which compared FDG-PET or PET/CT and WB-MRI in oncology were considered eligible for inclusion in this systematic review.

The exclusion criteria were: a) articles not within the field of interest of this review; b) review articles, editorials or letters, comments, conference proceedings; c) case reports or small case series (less than seven patients included); d) articles not in English, Spanish, French or German language; e) possible data overlap (in this case the most complete article was included).

Two researchers (MC and GT) reviewed the titles and the abstracts of the retrieved articles, applying the inclusion and exclusion criteria mentioned above. The full-text version of the retrieved articles was reviewed to confirm their eligibility for inclusion. Disagreements were resolved in a consensus meeting.

For each included study, information was collected concerning basic study (authors, journal, year of publication, country of origin, type of study), patient characteristics (number of patients, mean age, gender and type of tumours evaluated), methodological aspects about PET imaging (device used, injected activity, time between tracer injection and image acquisition, PET acquisition protocol, image analysis), methodological aspects about WB-MRI (field strength, sequences used, slice thickness, contrast media, diffusion-weighted imaging, apparent diffusion coefficient, acquisition time) and reference standard used.

Results

Literature search

The comprehensive literature search revealed 688 articles. Reviewing titles and abstracts, 644 articles were excluded applying the criteria mentioned above: 564 studies were excluded because not within the range of interest of this review; 69 articles were excluded because review articles, editorials or letters, comments, conference proceedings; 4 articles were excluded because case reports or small case series (less than seven patients included)6–9; 2 articles were excluded because not in English, Spanish, French or German language10,11; 5 articles were excluded for possible data overlap.12–16

Lastly, forty-four articles comprising 2287 patients were retrieved in full-text version and included in this systematic review (Figure 1).17–60 No additional studies were found screening the references of these articles.6–16 The characteristics of the included studies are presented in Tables 1–3.

FIGURE 1.

FIGURE 1.

Open in a new tab

Flow chart of the search for eligible studies on the comparison of FDG-PET or PET/CT and WB-MRI in oncology.

TABLE 1.

Basic studies and patient characteristics

Authors Year Country Study type No. of patients Mean Age % Male Type of tumors
Antoch et al.17 2003 Germany Prospective 98 58 64% Mixed
Schmidt et al.18 2005 Germany Prospective 41 56 44% Mixed
Komori et al.19 2007 Japan NR 16 66 70% Mixed
Li et al.20[18] 2007 China NR 30 48 37% Mixed
Brauck et al.21 2008 Germany Prospective 11 53 63% Mixed
Yang et al.22 2008 China NR 56 57 71% Mixed
Stecco et al.23 2009 Italy Prospective 29 NR NR Mixed
Krohmer et al.24 2010 Germany Prospective 24 11 NR Mixed
Fischer et al.25 2011 Switzerland Prospective 66 60 66% Mixed
Schmidt et al.26 2012 Germany Retrospective 135 61 45% Mixed
Cafagna et al.27 2012 Italy Retrospective 38 60 47% Mixed
Manenti et al.28 2012 Italy Retrospective 45 66 53% Mixed
Punwani et al.29 2010 England NR 31 13 58% Lymphoma
van Ufford et al.30 2011 Netherlands Prospective 22 49 68% Lymphoma
Abdulqadhr et al.31 2011 Sweden Prospective 31 47 64% Lymphoma
Gu et al.32 2011 China NR 17 50 65% Lymphoma
Lin et al.33 2011 France Prospective 15 48 60% Lymphoma
Wu et al.34 2011 Finland Prospective 8 54 50% Lymphoma
Chen et al.35 2012 China Prospective 10 45 40% Lymphoma
Shortt et al.36 2009 Ireland NR 24 67 46% Multiple Mieloma
Daldrup-Link et al.37 2001 Germany NR 39 13 69% Bone
Schmidt et al.38 2007 Germany Prospective 30 58 60% Bone
Ribrag et al.39 2008 France Prospective 47 50 50% Bone
Kumar et al.40 2008 India NR 26 NR NR Bone
Takenaka et al.41 2009 Japan Prospective 115 72 57% Bone
Heusner et al.42 2011 Germany Prospective 109 57 60% Bone
Ng et al.43 2010 Taiwan Prospective 179 47 75% Head and neck
O‘Neill et al.44 2010 Ireland Prospective 15 59 66% Head and neck
Ng et al.45 2011 Taiwan Prospective 79 52 88% Head and neck
Chan et al.46 2011 Taiwan Prospective 103 53 94% Head and neck
Eiber et al.47 2012 Germany Prospective 20 56 80% Head and neck
Plathow et al.48 2008 Germany NR 52 62 69% Lung
Ohno et al.49 2008 Japan Prospective 203 72 53% Lung
Yi et al.50 2008 Korea Prospective 165 61 72% Lung
Chen et al.51 2010 China NR 56 51 62% Lung
Pfannenberg et al.52 2007 Germany Prospective 64 58 41% Melanoma
Laurent et al.53 2010 France Prospective 35 NR NR Melanoma
Dellestable et al.54 2011 France Prospective 40 57 50% Melanoma
Schmidt et al.55 2008 Germany NR 33 55 0% Breast
Heusner et al.56 2010 Germany Prospective 20 54 0% Breast
Squillaci et al.57 2008 Italy NR 20 56 60% Colorectal
Schmidt et al.58 2009 Germany Retrospective 24 62 NR Colorectal
Giraudet et al.59 2007 France Prospective 55 56 62% Neuroendocrine tumors
Takano et al.60 2008 Japan Prospective 11 40 55% Neuroendocrine tumors
Open in a new tab

NR = not reported

TABLE 3.

Diagnostic performance of PET and WB-MRI in the included studies

Authors Sensitivity (%) Specificity (%) Accuracy(%)
PET MRI PET MRI PET MRI
Pt Les Pt Les Pt Les Pt Les Pt Les Pt Les
Antoch et al.17 NR NR NR NR NR NR NR NR NR NR NR NR
Schmidt et al.18 NR RS NR 89 NR RS NR 86 NR RS NR 88
Komori et al.19 NR NR NR NR NR NR NR NR NR NR NR NR
Li et al.20 NR NR NR NR NR NR NR NR NR NR NR NR
Brauck et al.21 NR NR NR NR NR NR NR NR NR NR NR NR
Yang et al.22 NR NR NR NR NR NR NR NR NR NR NR NR
Stecco et al.23 NR RS NR 87–89 NR RS NR 98–99 NR RS NR 97–99
Krohmer et al.24 NR RS NR 96 NR NR NR NR NR NR NR NR
Fischer et al.25 RS RS 85(WB-MRI), 88(DWI) 57(WB-MRI), 64(DWI) RS NR 81(WB-MRI), 69(DWI) NR RS NR 84(WB-MRI), 83(DWI) NR
Schmidt et al.26 94 NR 91 NR 97 NR 88 NR 96 NR 89 NR
Cafagna et al.27 NR NR NR NR NR NR NR NR NR NR NR NR
Manenti et al.28 NR RS NR 96(WB-MRI), 94(DWI) NR RS NR 100(WB-MRI), 100(DWI) NR RS NR 97(WB-MRI), 96(DWI)
Punwani et al.29 NR 100 (nodal) 96(extranodal) NR 98(nodal) 91(extranodal) NR 100(nodal) 100(extranodal) NR 99 (nodal) 99 (extranodal) NR 100 (nodal) 100(extranodal) NR 99 (nodal) 99(extranodal)
van Ufford et al.30 NR NR NR NR NR NR NR NR NR NR NR NR
Abdulqadhr et al.31 NR NR NR NR NR NR NR NR NR NR NR NR
Gu et al.32 NR RS NR 89(WB-MRI), 97(DWI) NR NR NR NR NR NR NR NR
Lin et al.33 NR NR NR NR NR NR NR NR NR NR NR NR
Wu et al.34 NR NR NR NR NR NR NR NR NR NR NR NR
Chen et al.35 NR NR NR NR NR NR NR NR NR NR NR NR
Shortt et al.36 NR 59 NR 68 NR 75 NR 83 NR 65 NR 74
Daldrup-Link et al.37 86 90 76 82 89 NR 100 NR 87 NR 87 NR
Schmidt et al.38 NR 98(N-stage), 82(M-stage) NR 80(N-stage), 96(M-stage) NR 83(N-stage), 82(M-stage) NR 75(N-stage), 82(M-stage) NR 96(TNM) NR 91(TNM)
Ribrag et al.39 100(bone lesions), 29 (bone marrow) 96(bone lesions), 95(bone marrow) 100(bone lesions), 100(bone marrow) 83(bone lesions), 90(bone marrow) NR NR NR NR NR NR NR NR
Kumar et al.40 NR 90 NR 97 NR 100 NR 99 NR 98 NR 99
Takenaka et al.41 96 97 64(WB-MRI), 96(DWI) 73(WB-MRI), 95(DWI) 86 95 90(WB-MRI) 79(DWI) 96(WB-MRI), 94(DWI) 88 95 84(WB-MRI), 83(DWI) 95(WB-MRI), 94(DWI)
Heusner et al.42 45 NR 64 NR 99 NR 94 NR 94 NR 91 NR
Ng et al.43 87 87 91 89 90 96 91 97 89 95 91 96
O‘Neill et al.44 NR NR NR NR NR NR NR NR NR NR NR NR
Ng et al.45 72 71 55 64 94 96 90 96 86 92 76 91
Chan et al.46 NR 81 NR 62 NR 99 NR 99 NR 99 NR 98
Eiber et al.47 NR NR NR NR NR NR NR NR NR NR NR NR
Plathow et al.48 92(T-stage), 96(N-stage), 100(M-stage) NR 100(T-stage), 88(N-stage), 100(M-stage) NR 100(T-stage), 100(N-stage), 100(M-stage) NR 100(T-stage), 96(N-stage), 100(M-stage) NR NR NR NR NR
Ohno et al.49 62–70 NR 56–60(WB-MRI), 57–67(DWI) NR 94 NR 92(WB-MRI), 88(DWI) NR 88–90 NR 86(WB-MRI), 82-84(DWI) NR
Yi et al.50 48 NR 52 NR 96 NR 94 NR 86 NR 86 NR
Chen et al.51 NR 98 NR 91 NR 98 NR 92 NR 97 NR 91
Pfannenberg et al.52 NR 90 NR 80 NR 77 NR 76 NR 87 NR 79
Laurent et al.53 NR 73 NR 83 NR 93 NR 98 NR NR NR NR
Dellestable et al.54 NR 74 NR 83 NR 89 NR 96 NR 74 NR 81
Schmidt et al.55 NR 91 NR 90 NR 90 NR 86 NR 91 NR 91
Heusner et al.56 75–100 94 66–100 91 94–100 99 0–100 72 93–100 98 30–100 76
Squillaci et al.57 NR NR NR NR NR NR NR NR NR NR NR NR
Schmidt et al.58 NR 86 NR 72 NR 96 NR 93 NR 91 NR 83
Giraudet et al.59 NR NR NR NR NR NR NR NR NR NR NR NR
Takano et al.60 NR NR NR NR NR NR NR NR NR NR NR NR
Open in a new tab

NR = not reported; Pt = per patient-based analysis; Les = per lesion-based analysis; DWI = diffusion weighted imaging; WB-MRI = whole body magnetic resonance imaging

Mixed tumours were evaluated in 12 articles17–28, lymphomas in 729–35; bone tumours in 736–42; head and neck tumours in 543–47; lung tumours in 448–51; melanoma in 352–54; breast cancer in 255,56; colorectal tumours in 257,58; neuroendocrine tumours in 2.59,60

Literature data discussion

Mixed tumours

First of all, Antoch et al.17 performing both FDG-PET/CT and WB-MRI in 98 patients with different malignancies, recommended the use of FDG-PET/CT as first-line whole-body imaging modality for tumour staging. In fact, the overall TNM stage was correctly determined in 75 cases with PET/CT (77%) and in 53 with WB-MRI (54%). Compared with WB-MRI, PET/CT had a direct impact on patient management in 12 patients. WB-MRI findings changed the therapy regimen in 2 patients compared with PET/CT.17

In 2005, Schmidt et al.18 evaluating 41 patients with mixed tumours using both methods found that WB-MRI was highly sensitive in detecting distant metastases (sensitivity was 96% for WB-MRI and 82% for FDG-PET/CT; specificity was 82% for both methods), whereas PET/CT was superior in lymph node staging (sensitivity was 98% for PET/CT and 80% for WB-MRI; specificity was 83% for PET/CT and 75% for WB-MRI). Accuracy for correct TNM staging was 96% for PET/CT and 91% for WB-MRI.18

In 2007 Komori et al.19 comparing FDG-PET/CT and DWI WB-MRI in 16 patients with malignant tumours reported that DWI WB-MRI may be useful in detecting malignancies, even if differentiating malignant and benign tumours may be difficult with this method. Twenty-five (92.6%) of the 27 malignant lesions were detected by DWI WBMRI whereas 22 malignant tumours (81.5%) were detected by FDG-PET/CT.19

Also Li et al.20 reported that DWI WB-MRI is a feasible imaging method in oncology, providing comparable results to PET imaging in 30 oncologic patients evaluated.

Brauck et al.21 evaluated a WB-MRI protocol by using unenhanced T2-weighted and contrast-enhanced T1-weighted real-time sequences during continuous table movement in 11 patients with FDG-PET/CT positive for metastases. Seventy-three of 75 metastases detected by PET/CT were correctly diagnosed by using WB-MRI, demonstrating the feasibility of this method in detecting metastases.21

In 2008, Yang et al.22 evaluated 56 patients with different tumours demonstrating the valuable role of DWI WB-MRI in tumour detection. Twelve patients underwent also FDG-PET. Among the diagnostic imaging methods DWI WB-MRI showed the highest sensitivity and specificity in detecting bone metastases. Among the twelve results compared with PET, eight were identical (concordance of 66.7%), one was found to be false-positive at MRI, two were found false-negative at MRI, one case was false-negative at PET and true-positive at MRI.22

In 2009, Stecco et al.23 compared FDG-PET/CT and DWI WB-MRI in staging 29 oncologic patients. Using FDG-PET/CT as reference standard, DWI WB-MRI interpreted by two readers had a sensitivity of 87–89%, a specificity of 98–99%, and an accuracy of 98–99%. These authors underlined the usefulness of DWI WB-MRI in cancer screening, staging, restaging and follow-up.23

Krohmer et al.24 evaluated 24 paediatric tumours with WB-MRI and FDG-PET, showing that WBMRI had high sensitivity for the detection of malignant disease. Overall 190 lesions were detected by WB-MRI and 155 lesions were found by FDG-PET. In patients with suspected bone lesions, WB-MRI should be considered for initial disease evaluation prior to specific and regional imaging methods to reduce the overall number of imaging examinations and radiation exposure.24

In 2011, Fischer et al.25 prospectively evaluated the diagnostic accuracy of WB-MRI with and without DWI compared with PET/CT (as reference standard) in 66 oncologic patients. PET/CT revealed 374 malignant lesions in 48/64 (75%) patients. Detection rates of WB-MRI with and without DWI were 84% and 64%, respectively. The detection rate was significantly higher with side-by-side analysis and fused image analysis compared with WB-MRI alone.25

Recently, Schmidt et al.26 demonstrated that both FDG-PET/CT and WB-MRI were efficient diagnostic triage methods in 135 patients planned for radioembolisation of liver metastases. Overall, FDG-PET/CT showed a higher diagnostic accuracy compared to WB-MRI. Both modalities, combined, exhibited high sensitivity for the diagnosis of extra-hepatic tumour manifestations. Patient-based sensitivity for detection of extra-hepatic disease was 94% for PET/CT and 91% for WB-MRI. Overall, by combining both modalities, the specificity for inclusion to radioembolisation therapy was 99%.26

Cafagna et al.27 evaluating 38 cancer patients demonstrated that DWI WB-MRI may be used in detecting tumours but is less effective in characterizing lymph nodal and bone lesions compared to FDG-PET/CT. The qualitative analysis of DWI WB-MRI and FDG-PET/CT showed that two patients were negative at both techniques. DWI WB-MRI was positive in 36 patients, 34 of whom were positive and two negative at FDG-PET/CT, respectively. A significant discordance was found between the two methods (255 lesions were identified by DWI WB-MRI and 184 by FDG-PET/CT).27

Lastly, Manenti et al.28 reported that DWI WB-MRI should be considered as alternative tool to conventional whole-body methods for tumour staging in cancer patients. Evaluating 45 patients using both methods, detection rates of malignancy did not differ between DWI WB-MRI and FDG-PET/CT.28

Lymphomas

Staging

Punwani et al.29 evaluated 31 subjects with lymphoma using both WB-MRI and enhanced FDG-PET/CT (used as reference standard) demonstrating that WB-MRI can accurately depict nodal and extranodal disease and may provide an alternative non-ionizing imaging method for initial staging. WB-MRI and enhanced PET/CT showed a good agreement for nodal and extranodal staging. The sensitivity and specificity of WB-MRI were 98% and 99%, respectively, for nodal disease; 91% and 99%, respectively, for extranodal disease.29

van Ufford et al.30 compared DWI WB-MRI with FDG-PET/CT in the staging of 22 patients with newly diagnosed lymphoma. These authors found a moderate overall agreement between DWI WB-MRI and FDG-PET/CT. Ann Arbor staging, according to DWI WB-MRI findings, was concordant with that of FDG PET/CT findings in 77% (17/22) of patients. In the care of patients with newly diagnosed lymphoma, staging with DWI WB-MRI did not result in underestimation of stage relative to the results with FDG-PET/CT. In a minority of patients, reliance on DWI WB-MRI led to clinically important overstaging relative to the results with FDG-PET/CT.30

Recently, Abdulqadhr et al.31 compared DWI WB-MRI with FDG-PET/CT in the staging of 31 lymphoma patients (8 with Hodgkin’s lymphoma and 23 with non-Hodgkin’s lymphomas). The staging was the same for DWI WB-MRI and FDG-PET/CT in 28 (90.3%) patients and different in three (9.7%). No Hodgkin lymphoma or aggressive non-Hodgkin’s lymphoma patients had different staging using both methods. Three indolent lymphocytic lymphomas had higher staging with DWI WB-MRI when compared with FDG-PET/CT.31

Gu et al.32 evaluated the diagnostic performance of WB-MRI with or without DWI in the detection of 17 patients with newly diagnosed lymphomas, using FDG-PET/CT as the reference standard. The addition of DWI to conventional WB-MRI improved diagnostic accuracy for lymphomas. These authors suggested that WB-MRI could be useful as an alternative method to FDG-PET/CT in the management of lymphomas.32

Treatment response assessment

Lin et al.33 assessed post-treatment changes in 15 patients with diffuse large B-cell lymphomas on DWI WB-MRI using PET/CT as the reference standard. After chemotherapy, among 85 examined lymph nodal regions, residual nodes were present in 62 (73%) regions on DWI WB-MRI. Of these 62 regions, 26 had persistent lymph nodes with longest transverse diameter > 10mm (MRI size criteria for positivity). Only 6 of these 26 regions were considered positive on PET/CT. DWI with ADC mapping showed a significant increase in ADC values of residual masses persisting after treatment and were helpful to assess the treatment response in patients with diffuse large B-cell lymphomas.33

Wu et al.34 evaluated the feasibility of DWI WB-MRI in the early chemotherapeutic response assessment of 8 patients with large B-cell lymphomas. These authors found that the results of WB-MRI with or without DWI were comparable with those of FDG-PET/CT.34

Recently, Chen et al.35 reported that DWI WB-MRI, combined with the dynamic changes of ADC value, was a valid alternative method compared to FDG PET/CT in assessing treatment response to chemotherapy in 10 patients with non-Hodgkin’s lymphoma.35

Bone tumours

Primary tumours

Shortt et al.36 found that WB-MRI performed better than FDG-PET/CT in the assessment of disease activity in 24 patients with multiple myeloma. FDG-PET/CT had a sensitivity of 59%, specificity of 75%, and accuracy of 65%. WB-MRI had a sensitivity of 68%, specificity of 83% and accuracy of 74%. In 62% of cases, FDG-PET/CT and WB-MRI findings were concordant. When PET and WB-MRI findings were concordant and positive, specificity was 100%.36

Bone metastases

Daldrup-Link et al.37 compared the diagnostic accuracy of WB-MRI and FDG-PET for the detection of bone metastases in 39 children. Sensitivity for the detection of bone metastases were 90% for FDG-PET and 82% for WB-MRI.37

In 2007, Schmidt et al.38 prospectively compared the diagnostic accuracy of WB-MRI and FDG-PET/CT for the detection of bone metastases in 30 patients with different oncologic diseases. WB-MRI showed a sensitivity, specificity and accuracy of 94%, 76% and 91%, respectively. PET/CT achieved a sensitivity, specificity and accuracy of 78%, 80% and 78%, respectively. Cut-off size for the detection of malignant bone lesions was 2 mm for WB-MRI and 5 mm for PET/CT.38

In 2008, Ribrag et al.39 suggested that non-invasive morphological procedures (WB-MRI and FDG-PET/CT) could be superior to bone marrow biopsy for bone marrow assessment in aggressive lymphomas. Both WB-MRI and PET/CT detected bone marrow lesions in the 9/43 patients, but two patients with multiple lesions had more lesions detected by PET/CT compared to MRI.39

Kumar et al.40 compared WB-MRI and FDG-PET/CT for the detection of bone marrow metastases in 26 children with small-cell neoplasms. WB-MRI showed a sensitivity, specificity and accuracy of 97.5%, 99.4%, and 99% respectively. FDG-PET/CT showed a sensitivity, specificity and accuracy of 90.0%, 100%, and 98%. Both WB-MRI and FDG-PET/CT showed excellent agreement with the final diagnosis.40

In 2009, Takenaka et al.41 prospectively compared WB-MRI (with and without DWI) and FDG-PET/CT in the detection of bone metastases in 115 patients with non-small cell lung cancer. These authors suggested that DWI WB-MRI can be used for bone metastases assessment in patients with non-small cell lung cancer being more accurate than bone scintigraphy and FDG-PET/CT.41

Recently, Heusner et al.42 found that FDG-PET/CT and WB-MRI were equally suitable for the detection of bone metastases in 109 patients with non-small cell lung cancer and malignant melanoma. The sensitivity, specificity, and accuracy for the detection of bone metastases was 45%, 99%, and 94% with FDG-PET/CT and 64%, 94%, and 91% with WB-MRI.42

Head and neck tumours

In 2010, Ng et al.43 prospectively compared WB-MRI and FDG-PET/CT for the detection of residual/recurrent nasopharyngeal carcinoma in 179 patients. On a per patient-based analysis, sensitivity and specificity of WB-MRI were similar to those of FDG-PET/CT (90.9% vs. 87.3%, and 91.1% vs. 90.3%, respectively). A combined interpretation of both methods increased the sensitivity to 94.5%.43

In the same year, O’Neill et al.44 compared WB-MRI and FDG-PET/CT for the staging of 15 patients with head and neck tumours. This study found radiological staging discordance between the two imaging modalities: T-staging showed a 74% of concordance, N-staging a 80% of concordance and M-stage a 100% of concordance.44

Recently, Ng et al.45 compared WB-MRI and FDG-PET/CT in 79 treated oropharyngeal or hypopharyngeal squamous cell carcinoma. PET/CT showed a trend towards higher diagnostic accuracy than WB-MRI in detecting residual/recurrent tumours or second primary tumours. The combined use of PET/CT and WB-MRI provided more added value to WB-MRI alone than to PET/CT alone. Sensitivity and specificity of FDG-PET/CT on a patient-based analysis were 72% and 94%. Sensitivity and specificity of WB-MRI on a patient-based analysis were 55% and 90%.45

The same group prospectively compared the diagnostic value of FDG-PET/CT and WB-MRI for the assessment of distant metastases and second primary cancers in 103 patients with untreated oropharyngeal or hypopharyngeal squamous cell carcinoma. Again, FDG-PET/CT showed a consistent trend toward higher sensitivity compared to WB-MRI for the detection of distant metastases and secondary primary cancers in these patients.46

Lastly, Eiber et al.47 reported that a combination of FDG-PET/CT and WB-MRI increased the diagnostic accuracy in the staging of 20 patients with head and neck tumours.47

Lung cancer

In 2008, Plathow et al.48 evaluated and compared FDG-PET/CT with WB-MRI in the correct staging of 52 patients with advanced non-small cell lung cancer (NSCLC). In the correct staging of advanced NSCLC, PET/CT had advantages in N-staging, whereas WB-MRI had certain advantages in T-staging. WB-MRI correctly T-staged all patients. PET/CT did not correctly stage chest wall infiltration in 4 cases (sensitivity: 92.3%; specificity: 100%). PET/CT correctly N-staged 51 patients (sensitivity: 96.1%; specificity: 100%). WB-MRI showed a significant tendency to understage N-status (sensitivity: 88.5%; specificity: 96.1%). In 2 patients, distant metastases were detected by both techniques.48

In the same year, Ohno et al.49 prospectively compared WB-MRI with and without DWI and FDG-PET/CT for M-stage assessment in 203 NSCLC patients. These authors found that DWI WB-MRI can be used for M-stage assessment in NSCLC patients with accuracy as good as that of PET/CT. The area under the ROC curve was 0.89 for FDG-PET/CT, 0.85 for DWI WB-MRI and 0.81 for WB-MRI without DWI, excluding brain metastases (due to the low accuracy of FDG-PET/CT in detecting brain metastases).49

Yi et al.51 prospectively compared the diagnostic accuracy of FDG-PET/CT and WB-MRI for TNM stage of 165 patients with NSCLC. WB-MRI was more useful for detecting brain and hepatic metastases, whereas PET/CT was more useful for detecting lymph node and soft-tissue metastases. Primary tumours (n=123 patients) were correctly staged in 101 (82%) patients at PET/CT and in 106 (86%) patients at WB-MRI. N stages (n=150 patients) were correctly determined in 105 (70%) patients at PET/CT and in 102 (68%) patients at WB-MRI. Thirty-one (20%) of 154 patients had metastatic lesions. Accuracy for detecting metastases was comparable between PET/CT and WB-MRI (86%). WB-MRI was more useful for detecting brain and hepatic metastases, whereas PET/CT was more useful for detecting lymph node and soft-tissue metastases.50

Chen et al.51 compared the diagnostic accuracy of DWI WB-MRI and FDG-PET/CT for assessment of 56 NSCLC patients. DWI WB-MRI was a feasible imaging method for the assessment of lymph nodal and metastatic spread with high accuracy, but it was limited in the evaluation of neck lymph nodal metastases and small metastatic lung nodules. Primary tumours were correctly detected in 56 (100%) patients by both PET/CT and DWI WB-MRI. Sensitivity, specificity and accuracy for lymph nodal metastases were 91%, 90% and 90% with DWI WB-MRI and 98%, 97% and 97% with PET/CT, respectively. Sensitivity, specificity and accuracy for other metastases were 90%, 95% and 92% with DWI WB-MRI and 98%, 100% and 98% with PET/CT.51

Melanoma

Pfannenberg et al.52 compared the diagnostic accuracy and impact on patient management of FDG-PET/CT and WB-MRI in staging of 64 patients with advanced melanoma. The overall accuracy of PET/CT was 86.7% compared to 78.8% for WB-MRI. PET/CT was significantly more accurate in N-staging and in detecting skin and subcutaneous metastases, whereas WB-MRI was more sensitive in detecting liver, bone and brain metastases. WB-MRI was less sensitive but more specific than PET/CT in classifying pulmonary lesions.52

Laurent et al.53 compared WB-MRI (with and without DWI) and FDG-PET/CT for staging of 35 patients with advanced melanoma. The sensitivity and specificity for WB-MRI without DWI were 82% and 97%, respectively, while for PET/CT were 72.8% and 92.7%, respectively. DWI allowed the detection of 14 supplementary malignant lesions (20%) in comparison with standard MRI protocol.51 In particular WB-MRI has been shown to be the most accurate method for detecting metastases in the liver, bone, subcutaneous and intra-peritoneal sites.53

Recently, Dellestable et al.54 found that DWI WB-MRI was superior compared to FDG-PET/CT in the staging of 40 patients with melanoma. Sensitivity and specificity were 74% and 89% for FDG-PET/CT, 83% and 96% for DWI WB-MRI. The sensitivity of MRI was distinctly superior compared to that of PET/CT for both hepatic and pulmonary lesions.54

Breast cancer

Schmidt et al.55 compared the diagnostic accuracy of WB-MRI and FDG-PET/CT for the detection of tumour recurrence in 33 patients with breast cancer. WB-MRI and PET/CT were both useful for the detection of tumour recurrence. WB-MRI was highly sensitive to detect distant metastatic disease. PET/CT was more sensitive in detecting lymph node involvement. Overall sensitivity was 91% for PET/CT and 90% for WB-MRI. Overall specificity was 90% for FDG-PET/CT and 86% for WB-MRI.55

Heusner et al.56 prospectively compared the diagnostic value of DWI WB-MRI and FDG-PET/CT for breast cancer staging in 20 patients. DWI resulted a sensitive but unspecific method for the detection of locoregional or metastatic breast cancer. These authors suggested that DWI WB-MRI is not alternative to FDG-PET/CT in staging breast cancer. The sensitivity, specificity, and accuracy for FDG-PET/CT were 94%, 99%, and 98%, respectively, whereas for DWI WB-MRI were 91%, 72%, and 76%, respectively.56

Colorectal cancer

Squillaci et al.57 assessed the accuracy of WB-MRI in comparison with FDG-PET/CT in staging 20 patients with colorectal carcinoma. These authors found that WB-MRI was a feasible method for staging colorectal cancer but could not substitute PET/CT. Lymph-nodal metastases were detected in 10/20 cases at WB-MRI and in 15/20 at PET/CT. M-stage was evaluated for liver metastases (27 lesions detected in 15 patients with WB/MRI; 23 lesions detected in 15 patients with PET/CT), lung metastases (19 lesions detected in 5 patients with WB-MRI, 25 lesions detected in 7 patients with PET/CT), and bone (9 lesions detected in 3 patients with both methods).57

Schmidt et al.58 assessed the diagnostic accuracy of WB-MRI compared with FDG-PET/CT in the follow-up of 24 patients suffering from colorectal cancer. Malignant foci were detected in 71% of patients with both methods. Lymph nodal metastases were better detected using PET/CT (sensitivity was 93% for PET/CT and 63% for WB-MRI), whereas distant metastases were depicted equally well by both investigations (sensitivity was 80% for PET/CT and 78% for WB-MRI). Overall sensitivity, specificity and diagnostic accuracy was 86%, 96% and 91% for PET/CT, and 72%, 93% and 83% for WB-MRI.58

Neuroendocrine tumours

Giraudet et al.59 comparing FDG-PET/CT and WB-MRI in 50 patients with suspected recurrent medullary thyroid carcinoma found a superior diagnostic accuracy of WB-MRI compared to FDG-PET/CT.59

Takano et al.60 found that DWI WB-MRI had a higher detection rate of metastatic lesions in 11 patients with paraganglioma when compared with metaiodobenzylguanidine scintigraphy or FDG-PET, particularly for lymph nodal and liver metastases. The limitations of DWI WB-MRI were possible false-positive findings and lower detectability of mediastinal lymph nodes and lung metastases.60

General remarks and conclusions

On the basis of our systematic review, we found several articles in which mixed tumour types were evaluated using both imaging methods.17–28 For what concerns the specific tumour types, more evidence exists for lymphomas29–35, bone tumours36–42, head and neck tumours43–47 and lung tumours48–51, whereas there is less evidence for other tumour types.

Overall, based on the literature findings, WB-MRI seems to be a valid alternative method compared to PET/CT in oncology. Nevertheless, it should be considered that the studies included in this systematic review were highly heterogeneous not only about the patient population evaluated (Table 1), but also for those technical aspects related to PET imaging and WB-MRI (Table 2). In particular, DWI, when performed, seemed to provide an added value to WB-MRI compared to FDG-PET/CT, increasing the sensitivity (due to a better lesion to background contrast).

TABLE 2.

Technical aspects of the included studies

Authors Device activity Injected Time between tracer injection and image acquisition (min) PET acquisition protocol Image analysis Field strenght (T) Sequences used Slice thickness Contrast media administration DWI ADC Acquisition time (min) Reference standard
Antoch et al.17 PET/CT 350 MBq 60 Static acquisition (3–5min per bed position) Qualitative 1.5 T1w(chest, abdomen), T2w(chest, abdomen), T1w(chest, abdomen)after CM, T2w(chest, abdomen)after CM 7mm Yes No No 26 Histology and/or follow up
Schmidt et al.18 PET/CT 200 MBq 60 Static acquisition (3min per bed position) Qualitative, semi-quantitative 1.5 STIR(WB), HASTE(chest), T1w(WB), 3D-VIBE(abdomen, pelvis)after CM 5mm Yes No No 55 Histology and PET/CT
Komori et al.19 PET/CT 3.7 MBq/kg 60 Static acquisition Qualitative, semi-quantitative 1.5 DW-EPI(WB) 6mm No Yes (Bvalue0-1000mm2/s) Yes 9 Histology and/or follow up
Li et al.20 PET NR NR Static aquisition Qualitative, semi-quantitative 1.5 DW-EPI-STIR(WB) 7mm No Yes (Bvalue0-800mm2/s) Yes 30 Follow up
Brauck et al.21 PET/CT 300–340 MBq 60 Static aquisition Qualitative 1.5 T1wSSFP(WB), T1wSSFP(WB) after CM, T2wSSFP(WB) 5mm Yes No No 6 PET/CT
Yang et al.22 PET NR NR Static acquisition Qualitative 1.5 DW-EPI-STIR(WB) 7mm No Yes (Bvalue0-400-600mm2/s) No 17–21 Follow up
Stecco et al.23 PET/CT 3.5 MBq/kg 60 Static acquisition Qualitative, semi-quantitative 1.5 DW-EPI-STIR(WB) 5mm No Yes (Bvalue0-500-1000mm2/s) No 20 PET/CT
Krohmer et al.24 PET NR NR Static aquisition Qualitative 1.5 T2w-STIR(WB), T1wTSE(WB) 6–8mm No No No 45 Follow up
Fischer et al.25 PET/CT 350 MBq 60 Static acquisition Qualitative 1.5 DW-EPI-FS(WB), T2wFIESTA(WB) 7mm No Yes (Bvalue0-700mm2/s) Yes 40 PET/CT
Schmidt et al.26 PET/CT 294 MBq 60 Static acquisition Qualitative, semi-quantitative 1.5 STIR(WB), HASTE(abdomen), HASTE(lung), STIR-lung, T2w-FS-TSE(liver), T1wTSE(WB), T1wTSE(spine), STIR(spine), VIBE(liver), T1-FS- GE(pelvis), T1wTSE(brain), T2wTSE(brain) 3–5mm Yes No No 51 Follow up
Cafagna et al.27 PET/CT 370–550 MBq 60 Static acquisition (3min per bed position) Qualitative, semi- quantitative 1.5 TSE(WB), DW-EPI-STIR(WB) 5mm No Yes (B-value0-500-1000mm2/s) Yes 51 Follow up
Manenti et al.28 PET/CT NR NR Static acquisition (4min per bed position) Qualitative 3.0 T1wTFE(WB), T2wTFE(WB), THRIVE- FFE(WB), DW-EPI-STIR(WB) 4–6mm Yes Yes (B-value0-1000mm2/s) No 35 Histology and/or follow up
Punwani et al.29 PET/CT 370 MBq 60 Static acquisition Qualitative, semi-quantitative 1.5 STIR-RARE(WB) 7mm No No No 25–30 PET/CT
van Ufford et al.30 PET/CT 3 MBq/kg 60 Static acquisition (3min per bed position) Qualitative 1.5 T1wTSE(WB), T1wSTIR(WB), DW-EPI(head, neck), DW-EPI-FS(chest, abdomen, pelvis) 6mm No Yes (Bvalue0-1000mm2/s) No 55 Follow up
Abdulqadhr et al.31 PET/CT 5 MBq/kg 60 Static acquisition (3min per bed position) Qualitative 1.5 T1wTSE(WB), T2wSTIR- FS, DWIBS(WB), T2wTSE, T1wGE(chest, abdomen) 6mm No Yes (Bvalue0-1000mm2/s) No 50 Histology and/or follow up
Gu et al.32 PET/CT 4.8 MBq/kg 60 Static acquisition (4min per bed position) Qualitative 3.0 T2wSPAIR-FS, DW-EPI-STIR 5mm No Yes (B-value0-1000mm2/sec) No 48 PET/CT
Lin et al.33 PET/CT 5 MBq/kg 60 Static acquisition (2min per bed position) Qualitative, semi-quantitative 1.5 DW-EPI-FS(WB) 5mm No Yes (Bvalue50-400-800mm2/s) Yes 30–45 PET/CT
Wu et al.34 PET/CT 370 MBq 60 Static acquisition (3min per bed position) Qualitative, semi-quantitative 3.0 T1wTSE(WB), T2wIR(WB), T1wGEVIBE(neck, abdomen), T1wGE-VIBE(neck, abdomen)after CM, T2wTSE(neck, abdomen), T2wTSE-FS(abdomen), DW-EPI(WB) 1–5mm Yes Yes (Bvalue0-800mm2/s) Yes 27 Follow up
Chen et al.35 PET and PET/CT NR NR NR NR 1.5 DW-EPI-STIR, FSE 6–7mm No Yes (B-value0-800mm2/s) Yes 43 Histology
Shortt et al.36 PET/CT 250–440 MBq 90 Static acquisition Qualitative, semi-quantitative 1.5 STIR(WB), T1wTSE(WB) 8mm No No No 20 Histology
Daldrup-Link et al.37 PET 3.7 MBq/kg 60 Static acquisition (4-6min per bed position) Qualitative 1.5 T1wSE, T2wSTIR-FS 4–6mm No No No 45–60 Histology and/or follow up
Schmidt et al.38 PET/CT 202–372 MBq 60 Static acquisition (3min per bed position) Qualitative, semi-quantitative 1.5 STIR(WB), HASTE-STIR(lung), T2wSE(liver), T1wSE(WB), T1w+STIR(spine), 3D-VIBE(liver)after CM, T1wGE-FS(abdomen)after CM, T1w+T2w(skull) 5mm Yes No No 55 Histology and/or follow up
Ribrag et al.39 PET/CT 539 MBq 46–184 Static acquisition (7–8min per bed position) Qualitative, semi-quantitative 1.5 STIR(WB), T1wSE(WB) 8mm No No No 20 Histology
Kumar et al.40 PET/CT 5.2 MBq/kg 45 Static acquisition Qualitative 1.5 SE-STIR(WB) NR No No No 40–60 Histology and/or follow up
Takenaka et al.41 PET/CT 3.3 MBq/kg 60 Static acquisition (2min per bed position) Qualitative, semi-quantitative 1.5 T1wGE(WB), T1wGE(WB)after CM, Opposed-phase T1 GE(WB), STIR- TSE(WB), DW-EPI-STIR(WB) 8mm Yes Yes (Bvalue0-1000mm2/s) No 75 Follow up
Heusner et al.42 PET/CT 260 MBq 60 Static acquisition (4–6min per bed position) Qualitative, semi-quantitative 1.5 T1wGE(chest, abdomen), T2wHASTE(chest, abdomen), T1wVIBE(abdomen)after CM, T1wVIBE(head, chest pelvis) after CM 3–7mm Yes No No NR Follow up
Ng et al.43 PET/CT 370 MBq 50–70 Static acquisition (3min per bed position) Qualitative 3.0 T2wTSE-FS(head, neck, T1wTSE(head, neck), T1wTSE(spine), STIR(spine)T1wTSE-WB, STIR-WB, T2wHASTE(chest, abdomen), T1wVIBE(abdomen), T1wVIBE(abdomen in artery, portal, equilibrium phase) after CM, T1wVIBE(chest, pelvis) after CM, T1wTSE-FS after CM 3–5mm Yes No No 37 Histology and/or follow up
O‘Neill et al.44 PET/CT NR NR NR Qualitative 1.5 NR NR NR No No 20 NR
Ng et al.45 PET/CT 370 MBq 50–70 Static acquisition (3min per bed position) Qualitative 3.0 T2wTSE-FS(head, neck), T1wTSE(head, neck), T1wTSE(spine), STIR(spine), T1wTSE(WB), STIR(WB), T2wHASTE(chest, abdomen), T1wVIBE(abdomen), T1wVIBE(abdomen)after CM, T1wVIBE(chest, pelvis)after CM, T1wTSE-FS after CM 3–5mm Yes No No 37 Histology and/or follow up
Chan et al.46 PET/CT 370 MBq 50–70 Static acquisition (2min per bed position) Qualitative, semi-quantitative 3.0 T2wTSE-FS(head, neck), T1wTSE(head, neck), T1wTSE(spine), STIR(spine)T1wTSE(WB), STIR(WB), T2wHASTE(chest, liver), T1wVIBE(abdomen), T1wVIBE(abdomen)after CM, T1wVIBE(chest, pelvis)after CM, T1wTSE-FS after CM 3–5mm Yes No No 50 Histology and/or follow up
Eiber et al.47 PET/CT 350–500 MBq 90 Static acquisition (2min per bed position) Qualitative 3.0 Dixon VIBE T1w(WB), T2 STIR(neck), T1 TSE(neck), T1 TSE after CM(neck), T1 TSE FS after CM(neck), VIBE T1w dynamic(liver), VIBE T1w after CM(lungs) 2.6–5mm Yes No No 23 Histology and/or follow up
Plathow et al.48 PET/CT 360–400 MBq 55–65 Static acquisition (3min per bed position) Qualitative 1.5 STIR(chest), VIBE-FS NR NR No No 60 Histology and/or follow up
Ohno et al.49 PET/CT 3.3 MBq/kg 60 Static acquisition (2min per bed position) Qualitative 1.5 T1wGE(WB), T1wGE(WB)after CM, Opposed-phase T1wGE(WB), STIR-TSE(WB, DW-EPI-STIR(WB) NR Yes Yes (Bvalue0-1000mm2/s) No 75 Histology and/or follow up
Yi et al.50 PET/CT 370 MBq 45 Static acquisition Qualitative 3.0 T2wTSE-FS(WB), T1wTFE(WB) after CM 4–8mm Yes No No 40 Histology and/or follow up
Chen et al.51 PET/CT 3.3 MBq/kg 60 Static acquisition Qualitative 1.5 DW-EPI(WB) 6mm No Yes (Bvalue0-1000mm2/s) No 12 Histology and/or follow up
Pfannenberg et al.52 PET/CT 370 MBq 55–65 Static acquisition (3min per bed position) Qualitative, semi-quantitative 1.5 NR NR NR No No NR Histology and/or follow up
Laurent et al.53 PET/CT 5.5 MBq/kg 60 Static acquisition (3–4 min per bed position Qualitative 1.5 2D-STIR(WB), 3D-T1w(WB)after CM, DW-EPI(WB) 7–8mm Yes Yes (Bvalue0-600mm2/s) No 60 Histology and/or follow up
Dellestable et al.54 PET/CT 5.5 MBq/kg 60 Static acquisition Qualitative, semi-quantitative 1.5 T2wSTIR(WB), T1(WB), DWI(WB), T1w3D-GE(WB)after CM NR Yes Yes (Bvalue NR) No 60 Histology and/or follow up
Schmidt et al.55 PET/CT 200 MBq 60 Static acqusition Qualitative, semi-quantitative 1.5–3.0 STIR(WB), HASTE(abdomen), HASTE(lung), STIR(lung), T2w-SE FS(liver), T1wTSE(WB), T1wTSE(spine), STIR(spine), Dyn. VIBE(liver)after CM, Static VIBE(lung, breast)after CM, T1wGE- FS(pelvis)after CM, T1wSE(brain) after CM, T1wGE(brain), T2wSE(brain)after CM NR Yes No No 43–52 Histology and/or follow up
Heusner et al.56 PET/CT 300 MBq 60 Static acquisition(4min per bed position) Qualitative, semi-quantitative 1.5 DW-EPI(WB), HASTE-FS(spine), DW-EPI(spine), T2wSPAIR(WB), T1wFLASH(WB), T2wHASTE(WB), T1wVIBE(WB)after CM 3–6mm Yes Yes (Bvalue50-600-800mm2/s) Yes NR Histology and/or follow up
Squillaci et al.57 PET/CT 370 MBq 45–60 Static acquisition (4min per bed position) Qualitative, semi-quantitative 3.0 T1wFFE(WB), T2wTSE(WB), T2wTSE- STIR(WB), THRIVE-SPAIR(WB), T1wFFE(WB)after CM 4–6mm Yes No No 47–55 Histology and/or clinical/imaging follow up
Schmidt et al.58 PET/CT 197–390 MBq 60 Static acquisition Qualitative, semi-quantitative 1.5–3.0 STIR(WB), T1wTSE(WB), HASTE(lung), STIR(lung), T2wTSE-FS(liver), STIR(spine), T1wTSE(spine), VIBE(liver)after CM, T1wTSE(brain) after CM, T2wTSE(brain)after CM, T1wGE-FS(abdomen)after CM 1.5–6mm Yes No No 42–51 Follow up
Giraudet et al.59 PET/CT 5 MBq/kg 60 Static acquisition Qualitative, semi-quantitative 1.5 T2wFSE(liver), dynamic contrast-enhanced MRI, T1-weighted sequences with fast multiplanar spoiled gradient-recalled echo imaging, STIR(WB), T1wSE(WB) 7mm No No No NR Follow up
Takano et al.60 PET 5 MBq/kg 50 Static acquisition (8min per bed position) Qualitative 1.5 T1wGE(WB), T2wFSE(WB), DW-EPI-STIR(WB) 4mm No Yes (Bvalue 0-1000mm2/s) No NR Histology and/or follow up
Open in a new tab

NR = not reported; CM = contrast media; DWIBS = diffusion weighted imaging with background body signal suppression; WB = whole-body

A possible limitation of some studies evaluated in this systematic review is the reference standard used. In fact, in some articles the diagnostic performance of WB-MRI was assessed considering PET or PET/CT as a reference standard. This is a possible source of bias, because FDG-PET or PET/CT has its own limitations, mainly due to the possibility of false-positive or false-negative results, which could affect the diagnostic accuracy calculated for WB-MRI (Table 3).

Possible advantages of WB-MRI compared to FDG-PET or PET/CT are: the lack of ionizing radiation, the higher soft-tissue contrast, the higher spatial resolution, the better assessment of non FDG-avid tumour types or sites of physiological FDG uptake. On the other hand, it should be considered that WB-MRI has a longer examination time compared to PET/CT and more variable acquisition protocols.

Both these imaging techniques still show limited worldwide availability if compared to other conventional imaging methods.

Referring to the costs, Plathow et al.61, performing a cost-analysis study, demonstrated that both whole-body imaging techniques allow substantial reduction of health care costs in many tumour types. On the basis of a simple full cost analysis, total costs of whole-body PET/CT were higher than those of whole-body MRI by a factor of about 2.0.61

Further larger prospective studies and in particular cost-effectiveness analysis comparing these two whole-body imaging techniques is needed to better assess the role of WB-MRI compared to FDG-PET or PET/CT in specific tumour types. Furthermore, emerging hybrid PET/MRI devices will increase the number of studies comparing PET to WB-MRI.

References

  • 1.Hodolic M. Role of F-18-choline PET/CT in evaluation of patients with prostate carcinoma. Radiol Oncol. 2011;45:17–21. doi: 10.2478/v10019-010-0050-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Basu S, Alavi A. Unparalleled contribution of 18F-FDG PET to medicine over 3 decades. J Nucl Med. 2008;49:17N–21N. 37N. [PubMed] [Google Scholar]
  • 3.Wang X, Xu M, Liang H, Xu LS. Comparison of CT and MRI in diagnosis of cerebrospinal leak induced by multiple fractures of skull base. Radiol Oncol. 2011;45:91–6. doi: 10.2478/v10019-011-0007-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Schmidt GP, Reiser MF, Baur-Melnyk A. Whole-body MRI for the staging and follow-up of patients with metastasis. Eur J Radiol. 2009;70:393–400. doi: 10.1016/j.ejrad.2009.03.045. [DOI] [PubMed] [Google Scholar]
  • 5.Lambregts DM, Maas M, Cappendijk VC, Prompers LM, Mottaghy FM, Beets GL, et al. Whole-body diffusion-weighted magnetic resonance imaging: Current evidence in oncology and potential role in colorectal cancer staging. Eur J Cancer. 2011;47:2107–16. doi: 10.1016/j.ejca.2011.05.013. [DOI] [PubMed] [Google Scholar]
  • 6.Thomson V, Pialat JB, Gay F, Coulon A, Voloch A, Granier A, et al. Whole-body MRI for metastases screening: a preliminary study using 3D VIBE sequences with automatic subtraction between noncontrast and contrast enhanced images. Am J Clin Oncol. 2008;31:285–92. doi: 10.1097/COC.0b013e31815e3ff4. [DOI] [PubMed] [Google Scholar]
  • 7.Mürtz P, Krautmacher C, Träber F, Gieseke J, Schild HH, Willinek WA. Diffusion-weighted whole-body MR imaging with background body signal suppression: a feasibility study at 3.0 Tesla. Eur Radiol. 2007;17:3031–7. doi: 10.1007/s00330-007-0717-8. [DOI] [PubMed] [Google Scholar]
  • 8.Seemann MD, Meisetschlaeger G, Gaa J, Rummeny EJ. Assessment of the extent of metastases of gastrointestinal carcinoid tumors using whole-body PET, CT, MRI, PET/CT and PET/MRI. Eur J Med Res. 2006;11:58–65. [PubMed] [Google Scholar]
  • 9.Furth C, Amthauer H, Denecke T, Ruf J, Henze G, Gutberlet M. Impact of whole-body MRI and FDG-PET on staging and assessment of therapy response in a patient with Ewing sarcoma. Pediatr Blood Cancer. 2006;47:607–11. doi: 10.1002/pbc.20662. [DOI] [PubMed] [Google Scholar]
  • 10.Yan RZ, Yang C, Zhang Q, Gu XM. [Whole-body diffusion weighted imaging manifestation of oral squamous cell carcinoma with metastatic lymph nodes]. [Chinese] Zhonghua Kou Qiang Yi Xue Za Zhi. 2009;44:144–6. [PubMed] [Google Scholar]
  • 11.Wang JW, Zhao S, Liu Y, Li J, Xu LM. [Preliminary study on the validity of whole body diffusion-weighted imaging for the detection of malignant lesions]. [Chinese] Zhonghua Kou Qiang Yi Xue Za Zhi. 2010;32:304–8. [PubMed] [Google Scholar]
  • 12.Lin C, Luciani A, Itti E, El-Gnaoui T, Vignaud A, Beaussart P, et al. Whole-body diffusion-weighted magnetic resonance imaging with apparent diffusion coefficient mapping for staging patients with diffuse large B-cell lymphoma. Eur Radiol. 2010;20:2027–38. doi: 10.1007/s00330-010-1758-y. [DOI] [PubMed] [Google Scholar]
  • 13.Schmidt GP, Baur-Melnyk A, Tiling R, Hahn K, Reiser MF, Schoenberg SO. [Comparison of high resolution whole-body MRI using parallel imaging and PET-CT. First experiences with a 32-channel MRI system.] [German] Radiologe. 2004;44:889–98. doi: 10.1007/s00117-004-1102-0. [DOI] [PubMed] [Google Scholar]
  • 14.Reiner CS, Fischer MA, Hany T, Stolzmann P, Nanz D, Donati OF, et al. Molecular imaging of malignant tumor metabolism: whole-body image fusion of DWI/CT vs. PET/CT. Acad Radiol. 2011;18:940–6. doi: 10.1016/j.acra.2011.03.010. [DOI] [PubMed] [Google Scholar]
  • 15.Ohno Y, Koyama H, Nogami M, Takenaka D, Yoshikawa T, Yoshimura M, et al. Whole-body MR imaging vs. FDG-PET: comparison of accuracy of M-stage diagnosis for lung cancer patients. J Magn Reson Imaging. 2007;26:498–509. doi: 10.1002/jmri.21031. [DOI] [PubMed] [Google Scholar]
  • 16.Ng SH, Chan SC, Yen TC, Chang JT, Liao CT, Ko SF, et al. Pretreatment evaluation of distant-site status in patients with nasopharyngeal carcinoma: accuracy of whole-body MRI at 3-Tesla and FDG-PET-CT. Eur Radiol. 2009;19:2965–76. doi: 10.1007/s00330-009-1504-5. [DOI] [PubMed] [Google Scholar]
  • 17.Antoch G, Vogt FM, Freudenberg LS, Nazaradeh F, Goehde SC, Barkhausen J, et al. Whole-body dual-modality PET/CT and whole-body MRI for tumor staging in oncology. JAMA. 2003;290:3199–206. doi: 10.1001/jama.290.24.3199. [DOI] [PubMed] [Google Scholar]
  • 18.Schmidt GP, Baur-Melnyk A, Herzog P, Schmid R, Tiling R, Schmidt M, et al. High-resolution whole-body magnetic resonance image tumor staging with the use of parallel imaging versus dual-modality positron emission tomography-computed tomography: experience on a 32-channel system. Invest Radiol. 2005;40:743–53. doi: 10.1097/01.rli.0000185878.61270.b0. [DOI] [PubMed] [Google Scholar]
  • 19.Komori T, Narabayashi I, Matsumura K, Matsuki M, Akagi H, Ogura Y, et al. 2-[Fluorine-18]-fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography versus whole-body diffusion-weighted MRI for detection of malignant lesions: initial experience. Ann Nucl Med. 2007;21:209–15. doi: 10.1007/s12149-007-0010-6. [DOI] [PubMed] [Google Scholar]
  • 20.Li S, Sun F, Jin ZY, Xue HD, Li ML. Whole-body diffusion-weighted imaging: technical improvement and preliminary results. J Magn Reson Imaging. 2007;26:1139–44. doi: 10.1002/jmri.21074. [DOI] [PubMed] [Google Scholar]
  • 21.Brauck K, Zenge MO, Vogt FM, Quick HH, Stock F, Trarbach T, et al. Feasibility of whole-body MR with T2- and T1-weighted real-time steady-state free precession sequences during continuous table movement to depict metastases. Radiology. 2008;246:910–6. doi: 10.1148/radiol.2463062017. [DOI] [PubMed] [Google Scholar]
  • 22.Yang TH, Lin JZ, Wang X, Lu JH, Chen Z. Preliminary study of feasibility of whole body diffusion weighted imaging in diagnosis of metastasis of tumor. Chin Med Sci J. 2008;23:187–92. doi: 10.1016/s1001-9294(09)60037-7. [DOI] [PubMed] [Google Scholar]
  • 23.Stecco A, Romano G, Negru M, Volpe D, Saponaro A, Costantino S, et al. Whole-body diffusion-weighted magnetic resonance imaging in the staging of oncologic patients: comparison with positron emission tomography computed tomography (PET-CT) in a pilot study. Radiol Med. 2009;114:1–17. doi: 10.1007/s11547-008-0348-4. [DOI] [PubMed] [Google Scholar]
  • 24.Krohmer S, Sorge I, Krausse A, Kluge R, Bierbach U, Marwede D, et al. Whole-body MRI for primary evaluation of malignant disease in children. Eur J Radiol. 2010;74:256–61. doi: 10.1016/j.ejrad.2009.01.037. [DOI] [PubMed] [Google Scholar]
  • 25.Fischer MA, Nanz D, Hany T, Reiner CS, Stolzmann P, Donati OF, et al. Diagnostic accuracy of whole-body MRI/DWI image fusion for detection of malignant tumours: a comparison with PET/CT. Eur Radiol. 2011;21:246–55. doi: 10.1007/s00330-010-1929-x. [DOI] [PubMed] [Google Scholar]
  • 26.Schmidt GP, Paprottka P, Jakobs TF, Hoffmann RT, Baur-Melnyk A, Haug A, et al. FDG-PET-CT and whole-body MRI for triage in patients planned for radioembolisation therapy. Eur J Radiol. 2012;81:269–76. doi: 10.1016/j.ejrad.2011.02.018. [DOI] [PubMed] [Google Scholar]
  • 27.Cafagna D, Rubini G, Iuele F, Maggialetti N, Notaristefano A, Pinto D, et al. Whole-body MR-DWIBS vs. [(18)F]-FDG-PET/CT in the study of malignant tumors: a retrospective study. Radiol Med. 2012;117:293–311. doi: 10.1007/s11547-011-0708-3. [DOI] [PubMed] [Google Scholar]
  • 28.Manenti G, Cicciò C, Squillaci E, Strigari L, Calabria F, Danieli R, et al. Role of combined DWIBS/3D-CE-T1w whole-body MRI in tumor staging: Comparison with PET-CT. Eur J Radiol. 2012 doi: 10.1016/j.ejrad.2011.08.005. [DOI] [PubMed] [Google Scholar]
  • 29.Punwani S, Taylor SA, Bainbridge A, Prakash V, Bandula S, De Vita E, et al. Pediatric and adolescent lymphoma: comparison of whole-body STIR half-Fourier RARE MR imaging with an enhanced PET/CT reference for initial staging. Radiology. 2010;255:182–90. doi: 10.1148/radiol.09091105. [DOI] [PubMed] [Google Scholar]
  • 30.van Ufford HM, Kwee TC, Beek FJ, van Leeuwen MS, Takahara T, Fijnheer R, et al. Newly diagnosed lymphoma: initial results with whole-body T1-weighted, STIR, and diffusion-weighted MRI compared with 18F-FDG PET/CT. AJR Am J Roentgenol. 2011;196:662–9. doi: 10.2214/AJR.10.4743. [DOI] [PubMed] [Google Scholar]
  • 31.Abdulqadhr G, Molin D, Aström G, Suurküla M, Johansson L, Hagberg H, et al. Whole-body diffusion-weighted imaging compared with FDG-PET/CT in staging of lymphoma patients. Acta Radiol. 2011;52:173–80. doi: 10.1258/ar.2010.100246. [DOI] [PubMed] [Google Scholar]
  • 32.Gu J, Chan T, Zhang J, Leung AY, Kwong YL, Khong PL. Whole-body diffusion-weighted imaging: the added value to whole-body MRI at initial diagnosis of lymphoma. AJR Am J Roentgenol. 2011;197:w384–91. doi: 10.2214/AJR.10.5692. [DOI] [PubMed] [Google Scholar]
  • 33.Lin C, Itti E, Luciani A, Zegai B, Lin SJ, Kuhnowski F, et al. Whole-body diffusion-weighted imaging with apparent diffusion coefficient mapping for treatment response assessment in patients with diffuse large B-cell lymphoma:pilot study. Invest Radiol. 2011;46:341–9. doi: 10.1097/RLI.0b013e3182087b03. [DOI] [PubMed] [Google Scholar]
  • 34.Wu X, Kellokumpu-Lehtinen PL, Pertovaara H, Korkola P, Soimakallio S, Eskola H, et al. Diffusion-weighted MRI in early chemotherapy response evaluation of patients with diffuse large B-cell lymphoma--a pilot study: comparison with 2-deoxy-2-fluoro-D-glucose-positron emission tomography/computed tomography. NMR Biomed. 2011;24:1181–90. doi: 10.1002/nbm.1689. [DOI] [PubMed] [Google Scholar]
  • 35.Chen Y, Zhong J, Wu H, Chen N. The clinical application of whole-body diffusion-weighted imaging in the early assessment of chemotherapeutic effects in lymphoma: the initial experience. Magn Reson Imaging. 2012;30:165–70. doi: 10.1016/j.mri.2011.09.019. [DOI] [PubMed] [Google Scholar]
  • 36.Shortt CP, Gleeson TG, Breen KA, McHugh J, O’Connell MJ, O’Gorman PJ, et al. Whole-Body MRI versus PET in assessment of multiple myeloma disease activity. AJR Am J Roentgenol. 2009;192:980–6. doi: 10.2214/AJR.08.1633. [DOI] [PubMed] [Google Scholar]
  • 37.Daldrup-Link HE, Franzius C, Link TM, Laukamp D, Sciuk J, Jürgens H, et al. Whole-body MR imaging for detection of bone metastases in children and young adults: comparison with skeletal scintigraphy and FDG PET. AJR Am J Roentgenol. 2001;177:229–36. doi: 10.2214/ajr.177.1.1770229. [DOI] [PubMed] [Google Scholar]
  • 38.Schmidt GP, Schoenberg SO, Schmid R, Stahl R, Tiling R, Becker CR, et al. Screening for bone metastases: whole-body MRI using a 32-channel system versus dual-modality PET-CT. Eur Radiol. 2007;17:939–49. doi: 10.1007/s00330-006-0361-8. [DOI] [PubMed] [Google Scholar]
  • 39.Ribrag V, Vanel D, Leboulleux S, Lumbroso J, Couanet D, Bonniaud G, et al. Prospective study of bone marrow infiltration in aggressive lymphoma by three independent methods: whole-body MRI, PET/CT and bone marrow biopsy. Eur J Radiol. 2008;66:325–31. doi: 10.1016/j.ejrad.2007.06.014. [DOI] [PubMed] [Google Scholar]
  • 40.Kumar J, Seith A, Kumar A, Sharma R, Bakhshi S, Kumar R, et al. Whole-body MR imaging with the use of parallel imaging for detection of skeletal metastases in pediatric patients with small-cell neoplasms: comparison with skeletal scintigraphy and FDG PET/CT. Pediatr Radiol. 2008;38:953–62. doi: 10.1007/s00247-008-0921-y. [DOI] [PubMed] [Google Scholar]
  • 41.Takenaka D, Ohno Y, Matsumoto K, Aoyama N, Onishi Y, Koyama H, et al. Detection of bone metastases in non-small cell lung cancer patients: comparison of whole-body diffusion-weighted imaging (DWI), whole-body MR imaging without and with DWI, whole-body FDG-PET/CT, and bone scintigraphy. J Magn Reson Imaging. 2009;30:298–308. doi: 10.1002/jmri.21858. [DOI] [PubMed] [Google Scholar]
  • 42.Heusner T, Gölitz P, Hamami M, Eberhardt W, Esser S, Forsting M, et al. “One-stop-shop” staging: should we prefer FDG-PET/CT or MRI for the detection of bone metastases? Eur J Radiol. 2011;78:430–5. doi: 10.1016/j.ejrad.2009.10.031. [DOI] [PubMed] [Google Scholar]
  • 43.Ng SH, Chan SC, Yen TC, Liao CT, Chang JT, Ko SF, et al. Comprehensive imaging of residual/recurrent nasopharyngeal carcinoma using whole-body MRI at 3 T compared with FDG-PET-CT. Eur Radiol. 2010;20:2229–40. doi: 10.1007/s00330-010-1784-9. [DOI] [PubMed] [Google Scholar]
  • 44.O’Neill JP, Moynagh M, Kavanagh E, O’Dwyer T. Prospective, blinded trial of whole-body magnetic resonance imaging versus computed tomography positron emission tomography in staging primary and recurrent cancer of the head and neck. J Laryngol Otol. 2010;124:1274–7. doi: 10.1017/S0022215110001398. [DOI] [PubMed] [Google Scholar]
  • 45.Ng SH, Chan SC, Yen TC, Liao CT, Lin CY, Tung-Chieh Chang J, et al. PET/CT and 3-T whole-body MRI in the detection of malignancy in treated oropharyngeal and hypopharyngeal carcinoma. Eur J Nucl Med Mol Imaging. 2011;38:996–1008. doi: 10.1007/s00259-011-1740-1. [DOI] [PubMed] [Google Scholar]
  • 46.Chan SC, Wang HM, Yen TC, Lin CY, Chin SC, Liao CT, et al. 18F-FDG PET/CT and 3.0-T whole-body MRI for the detection of distant metastases and second primary tumours in patients with untreated oropharyngeal/hypopharyngeal carcinoma: a comparative study. Eur J Nucl Med Mol Imaging. 2011;38:1607–19. doi: 10.1007/s00259-011-1824-y. [DOI] [PubMed] [Google Scholar]
  • 47.Eiber M, Souvatzoglou M, Pickhard A, Loeffelbein DJ, Knopf A, Holzapfel K, et al. Simulation of a MR-PET protocol for staging of head-and-neck cancer including Dixon MR for attenuation correction. Eur J Radiol. 2012;81:2658–65. doi: 10.1016/j.ejrad.2011.10.005. [DOI] [PubMed] [Google Scholar]
  • 48.Plathow C, Aschoff P, Lichy MP, Eschmann S, Hehr T, Brink I, et al. Positron emission tomography/computed tomography and whole-body magnetic resonance imaging in staging of advanced nonsmall cell lung cancer—initial results. Invest Radiol. 2008;43:290–7. doi: 10.1097/RLI.0b013e318163273a. [DOI] [PubMed] [Google Scholar]
  • 49.Ohno Y, Koyama H, Onishi Y, Takenaka D, Nogami M, Yoshikawa T, et al. Non-small cell lung cancer: whole-body MR examination for M-stage assessment--utility for whole-body diffusion-weighted imaging compared with integrated FDG PET/CT. Radiology. 2008;248:643–54. doi: 10.1148/radiol.2482072039. [DOI] [PubMed] [Google Scholar]
  • 50.Yi CA, Shin KM, Lee KS, Kim BT, Kim H, Kwon OJ, et al. Non-small cell lung cancer staging: efficacy comparison of integrated PET/CT versus 3.0-T whole-body MR imaging. Radiology. 2008;248:632–42. doi: 10.1148/radiol.2482071822. [DOI] [PubMed] [Google Scholar]
  • 51.Chen W, Jian W, Li HT, Li C, Zhang YK, Xie B, et al. Whole-body diffusion-weighted imaging vs. FDG-PET for the detection of non-small-cell lung cancer. How do they measure up? Magn Reson Imaging. 2010;28:613–70. doi: 10.1016/j.mri.2010.02.009. [DOI] [PubMed] [Google Scholar]
  • 52.Pfannenberg C, Aschoff P, Schanz S, Eschmann SM, Plathow C, Eigentler TK, et al. Prospective comparison of 18F-fluorodeoxyglucose positron emission tomography/computed tomography and whole-body magnetic resonance imaging in staging of advanced malignant melanoma. Eur J Cancer. 2007;43:557–64. doi: 10.1016/j.ejca.2006.11.014. [DOI] [PubMed] [Google Scholar]
  • 53.Laurent V, Trausch G, Bruot O, Olivier P, Felblinger J, Régent D. Comparative study of two whole-body imaging techniques in the case of melanoma metastases: advantages of multi-contrast MRI examination including a diffusion-weighted sequence in comparison with PET-CT. Eur J Radiol. 2010;75:376–83. doi: 10.1016/j.ejrad.2009.04.059. [DOI] [PubMed] [Google Scholar]
  • 54.Dellestable P, Granel-Brocard F, Rat AC, Olivier P, Régent D, Schmutz JL. [Impact of whole body magnetic resonance imaging (MRI) in the management of melanoma patients, in comparison with positron emission tomography/computed tomography (TEP/CT) and CT.] [French] Ann Dermatol Venereol. 2011;138:377–83. doi: 10.1016/j.annder.2011.02.023. [DOI] [PubMed] [Google Scholar]
  • 55.Schmidt GP, Baur-Melnyk A, Haug A, Heinemann V, Bauerfeind I, Reiser MF, et al. Comprehensive imaging of tumor recurrence in breast cancer patients using whole-body MRI at 1.5 and 3 T compared to FDG-PET-CT. Eur J Radiol. 2008;65:47–58. doi: 10.1016/j.ejrad.2007.10.021. [DOI] [PubMed] [Google Scholar]
  • 56.Heusner TA, Kuemmel S, Koeninger A, Hamami ME, Hahn S, Quinsten A, et al. Diagnostic value of diffusion-weighted magnetic resonance imaging (DWI) compared to FDG PET/CT for whole-body breast cancer staging. Eur J Nucl Med Mol Imaging. 2010;37:1077–86. doi: 10.1007/s00259-010-1399-z. [DOI] [PubMed] [Google Scholar]
  • 57.Squillaci E, Manenti G, Mancino S, Cicciò C, Calabria F, Danieli R, et al. Staging of colon cancer: whole-body MRI vs. whole-body PET-CT--initial clinical experience. Abdom Imaging. 2008;33:676–88. doi: 10.1007/s00261-007-9347-5. [DOI] [PubMed] [Google Scholar]
  • 58.Schmidt GP, Baur-Melnyk A, Haug A, Utzschneider S, Becker CR, Tiling R, et al. Whole-body MRI at 1.5 T and 3 T compared with FDG-PET-CT for the detection of tumour recurrence in patients with colorectal cancer. Eur Radiol. 2009;19:1366–78. doi: 10.1007/s00330-008-1289-y. [DOI] [PubMed] [Google Scholar]
  • 59.Giraudet AL, Vanel D, Leboulleux S, Aupérin A, Dromain C, Chami L, et al. Imaging medullary thyroid carcinoma with persistent elevated calcitonin levels. J Clin Endocrinol Metab. 2007;92:4185–90. doi: 10.1210/jc.2007-1211. [DOI] [PubMed] [Google Scholar]
  • 60.Takano A, Oriuchi N, Tsushima Y, Taketomi-Takahashi A, Nakajima T, Arisaka Y, et al. Detection of metastatic lesions from malignant pheochromocytoma and paraganglioma with diffusion-weighted magnetic resonance imaging: comparison with 18F-FDG positron emission tomography and 123I-MIBG scintigraphy. Ann Nucl Med. 2008;22:395–401. doi: 10.1007/s12149-008-0128-1. [DOI] [PubMed] [Google Scholar]
  • 61.Plathow C, Walz M, Lichy MP, Aschoff P, Pfannenberg C, Bock H, et al. [Cost considerations for whole-body MRI and PET/CT as part of oncologic staging.] [German] Radiologe. 2008;48:384–96. doi: 10.1007/s00117-007-1547-z. [DOI] [PubMed] [Google Scholar]

Articles from Radiology and Oncology are provided here courtesy of De Gruyter

RESOURCES