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To assess the added information gained from computed tomography (CT) or magnetic resonance imaging (MRI) of the abdomen over abdominal ultrasound in children undergoing staging of Wilms’ tumours.
Titlu original
Added Value of Abdominal Cross-sectional Imaging (CT or MRI) in Staging of Wilms’ Tumours
To assess the added information gained from computed tomography (CT) or magnetic resonance imaging (MRI) of the abdomen over abdominal ultrasound in children undergoing staging of Wilms’ tumours.
To assess the added information gained from computed tomography (CT) or magnetic resonance imaging (MRI) of the abdomen over abdominal ultrasound in children undergoing staging of Wilms’ tumours.
K. McDonald a, * , P. Duffy b , T. Chowdhury c , K. McHugh a a Department of Paediatric Radiology, The Royal London Hospital, London, UK b Department of Urology, Great Ormond Street Hospital for Children, London, UK c Department of Oncology, Great Ormond Street Hospital for Children, London, UK arti cle informati on Article history: Received 23 January 2012 Received in revised form 17 April 2012 Accepted 1 May 2012 AIM: To assess the added information gained from computed tomography (CT) or magnetic resonance imaging (MRI) of the abdomen over abdominal ultrasound in children undergoing staging of Wilms tumours. MATERIALS AND METHOD: Fifty-two consecutive patients with histologically proven Wilms tumours were identied. Each had an initial staging abdominal ultrasound followed by either a CT or MRI examination of the abdomen. Details including tumour size, site, and character- istics, presence of lymph nodes, local invasion, evidence of nephroblastomatosis, and any other relevant nding were gathered from the report of each ultrasound and CT or MRI. Each CT/MRI was then re-reviewed by a consultant paediatric radiologist and a paediatric radiology fellow. The difference in ndings between the ultrasound and cross-sectional imaging were noted. RESULTS: Twelve patients were excluded from the study because the CT/MRI was performed before the ultrasound, or imaging was incomplete. Twenty-six patients were female, 14 male. The ages ranged from 9 months to 10.8 years (mean 3.75 years). Twenty-one patients out of the remaining 40 had additional ndings detected on the CT or MRI examination that had not been reported on the ultrasound. The most important additional ndings included three patients with nephroblastomatosis and two with contralateral tumours. Other ndings included two patients with tumour haemorrhage, four with abdominal lymph node enlarge- ment, three with inferior vena cava (IVC)/renal vein thrombus, four with adjacent organ invasion, one patient where the origin of the abdominal tumour was conrmed as renal, and one patient where possible liver invasion was excluded. CONCLUSION: In over half the patients, CT or MRI added additional information in the local staging of Wilms tumours. Sole reliance on ultrasound for Wilms staging risks missing signicant abnormalities. 2012 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved. Introduction Wilms tumour is the commonest malignant tumour arising from the kidney in childhood, and the prognosis has improved dramatically in recent years. The management of Wilms tumours differs in Europe and North America. In European countries and elsewhere treatment strategies are based on the International Society of Paediatric Oncology (SIOP) protocols, where chemotherapy is followed by surgery. This favours tumour reduction prior to surgical resection, thus reducing the risk of tumour spill/rupture at the time of surgery, 1 as well as reducing surgical stage, and therefore, potentially, the intensity of postoperative * Guarantor and correspondent: K. McDonald, Department of Paedi- atric Radiology, The Royal London Hospital, London E1 1BB, UK. Tel.: 44 (0) 7793750803; fax: 44 (0) 2078298665. E-mail address: kmcdonald@doctors.org.uk (K. McDonald). Contents lists available at SciVerse ScienceDirect Clinical Radiology j ournal homepage: www. cl i ni cal radi ol ogyonl i ne. net 0009-9260/$ e see front matter 2012 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved. http://dx.doi.org/10.1016/j.crad.2012.05.006 Clinical Radiology 68 (2013) 16e20 chemotherapy. In North America management is based on the National Wilms Tumour Study Group (NWTSG) guide- lines, which advocates surgery prior to chemotherapy. 1 The outcomes for each strategy are similar. 2 Formal tumour staging is done at the time of surgery. 3 However, assessment of localized versus metastatic disease at presentation will determine the intensity of preoperative chemotherapy according to the European SIOP strategy, and must include imaging of the primary and metastatic sites. According to the European SIOP protocol, imaging of the primary includes ultrasound as mandatory, and CT/MRI abdomen is strongly advised in the UK or if further detail is required. Chest x-ray is mandatory for assessment of meta- static sites and chest CT for doubtful metastases, although chest CT is highly recommended for all patients in the UK. Abdominal imaging at the time of presentation provides valuable information ontumour origin, size, extent, invasion of adjacent structures; presence of tumour thrombus in the renal vein, inferior vena cava (IVC) and right atrium; the presence of contralateral tumour(s) or nephrogenic rests; lymph node enlargement; tumour rupture; and metastatic spread to the liver. 4 Preoperative imaging undoubtedly aids surgical planning and in Europe it is extremely important in the assessment of tumour response to preoperative chemotherapy. This is particularly relevant in the case of bilateral Wilms tumours where further courses of chemo- therapy in chemoresponsive tumours may improve the chances of nephron-sparing surgery being possible. The preferred imaging strategy for abdominal staging varies across Europe. Some countries, such as the Netherlands (R. van Rijn, pers. comm.), may rely mainly on abdominal ultrasound, whilst other countries, including the UK, use either CT or MRI of the abdomen, in addition to routine ultrasound in every patient at presentation and for preoperative tumour response assessment and surgical planning. In a retrospective observational study, the added information gained from CT or MRI of the abdomen at the time of presentation in children undergoing abdominal staging for Wilms tumours was assessed at our institution a tertiary paediatric oncology centre in the UK. Materials and methods Ethical approval was not considered necessary by the local Ethics Committee, but the study was registered with the local Research and Development ofce. Fifty-two consecutive patients with histologically proven Wilms tumours were identiedretrospectively. Eachhad an initial diagnostic abdominal ultrasound (performed either by consultant paediatric radiologists or senior paediatric radiology trainees and experienced paediatric sonographers withreviewby the consultant) followedbyeither a CTor MRI examination of the abdomen, depending on the availability of the machines, anaesthetic team, and patient MRI safety issues. A subsequent preoperative ultrasound followed by either CT or MRI were performed after chemotherapy. Chil- dren who had their CT/MRI prior to the ultrasound were excluded as this may have biased the ultrasound ndings (this occurred on some occasions at this institution when patients were transferred from other institutions, with cross-sectional imagingperformedelsewhere). Inthereport, the presence or absence of specic ndings from each examination were sought. These included tumour size, site, origin and characteristics; presence of enlarged lymph nodes; local invasion; evidence of nephroblastomatosis in the ipsilateral or contralateral kidney; anyother abnormality of the contralateral kidney; and any other relevant nding. Each CT/MRI was then re-reviewed by a consultant paedi- atric radiologist and paediatric radiology fellow. The ultra- sound images were not re-reviewed as it is an operator- dependent technique, where the ndings are usually docu- mentedwitha fewrepresentative images andfurther review seldom nds signicant ndings that were not reported at the time of the examination. The report for the ultrasound examination is thus largely taken at face value, and this is generally accepted at the weekly multidisciplinary team (MDT) oncology meeting. The difference in ndings between the initial diagnostic ultrasound and cross-sectional imaging were noted and correlation was made with the histopathology results and surgical ndings. Results Twelve patients were excluded from the study because the CT/MRI was performed before the ultrasound, or the patients imaging was incomplete. Twenty-six patients were female, 14 male. Their ages ranged from 9 months to 10.8 years (mean 3.75 years). Eighteen patients out of the remaining 40 had 19 additional ndings detected on the CT (n 22) or MRI (n 18) examination that had not been reported on the ultrasound, and were conrmed at the time of resection or at histology. The most important additional ndings included two patients with contralateral tumours (Fig 1), one with an additional ipsilateral tumour, and three with contralateral nephroblastomatosis (Fig 2). Other ndings included two patients with tumour haemorrhage/ rupture, three with abdominal lymph node enlargement, two with IVC/renal vein thrombus, four with adjacent organ adhesion/possible invasion (Fig 3), one patient where the origin of the abdominal tumour was difcult to determine on ultrasound was conrmed as renal and one patient where possible liver invasion was excluded (Fig 4). On correlation with the histology results and surgical ndings ve patients were found to have false-negative results, and six patients were found to have false-positive results on cross-sectional imaging. The false-negative results included two patients found to have IVC thrombus, and three patients with enlarged abdominal lymph nodes at the time of surgery. The false-positive results included one patient each with a contained tumour rupture, IVC thrombus, lymph node enlargement, psoas invasion, liver metastasis, and adrenal invasion that were not conrmed at surgery or at histology. K. McDonald et al. / Clinical Radiology 68 (2013) 16e20 17 The time difference between the initial diagnostic imaging and surgical resection ranged from 1 week to 5 months. For the patients with false-negative and false- positive ndings on cross-sectional imaging, the range was 1e8 weeks (mean 4.5 weeks). Discussion Ultrasound is a non-invasive technique, does not involve irradiation, or require sedation, and should be the rst-line investigation of patients with suspected abdominal tumours. It also has excellent capacity to assess the renal vein and IVC for tumour thrombus extension. However, it is operator-dependent, requires a co-operative child, and has other limitations; for example, bowel gas may obscure the retroperitoneum rendering assessment of lymph nodes difcult or impossible. Cross-sectional imaging with CT or MRI provides excel- lent anatomical detail. 5,6 Although todays modern MRI systems enable much shorter examination times, most young patients with Wilms masses will require sedation or general anaesthesia, which are not without risk. Many of those who undergo CT may not require sedation but CT has the additional disadvantage of a radiation burden. In some European countries, only abdominal ultrasound, plus chest radiography, is used for staging Wilms tumours prior to chemotherapy. However, the extra anatomical detail available with CT or MRI has resulted in these becoming part of the routine abdominal staging protocol in the majority of European countries, including the UK, and in North America. Indeed, it is undoubtedly better practice to corroborate positive or negative ndings in these children (such as metastases or no hepatic metastases) with two imaging techniques, rather than relying solely on ultrasound. Oncologists at our institution insist on the additional information afforded by CT or MRI in this study, with MRI being optimal for the reasons described above. MRI has informed situations where the tumour origin was uncertain and the diagnosis in question, thus inuencing oncological and surgical management. The existence of contralateral tumours or nephroblastomatosis, particularly in the syn- dromic child, will also inuence oncological management and surgical planning, as well as surveillance during and after treatment. 7 This study contains a number of deciencies. It is retro- spective. The ultrasound studies were not individually reviewed, although the CT and MRI studies were, for the reasons already stated above. It is likely that the ultrasound results were known to those reporting the CT or MRI, whilst the ultrasound studies were the rst examination, when Figure 1 A 2-year-old male patient with chromosome 11 deletion, undergoing surveillance due to increased risk of developing Wilms tumours. T2-weighted, fat-saturated, axial image. Horseshoe kidney with hydronephrosis of the right moiety due to tumour extending into the right renal pelvis (not shown on this section, but identied on ultrasound), and a 2 cm rounded lesion, with intermediate signal in the lower part of the left moiety, close to the isthmus (arrow; not identied on ultrasound). Figure 2 An 8-month-old male patient with large, left-sided mass. (a) Longitudinal ultrasound image of the right kidney, which appears normal. (b) Coronal, contrast-enhanced, fat-suppressed image showing the large left-sided renal tumour, and a small low signal lesion medially in the right kidney (arrow), in keeping with contra- lateral nephroblastomatosis. K. McDonald et al. / Clinical Radiology 68 (2013) 16e20 18 information about the patients would have been limited. Not all the patients had repeat pre-surgical CT or MRI. There was an inevitable delay between initial imaging and later surgery or histology assessment. The false-negative results are probably acceptable as involved lymph nodes, in particular, are typically immediately adjacent to the tumour and indistinguishable from the primary lesion at initial diagnosis. The false positives may be false because there has been chemotherapy and the passage of time between CT or MRI assessment and surgery or histological conrmation. There is a growing body of opinion within oncology and radiology circles that the traditional prose-style radiology report may be becoming inadequate. Traditional reports frequently omit key facts essential for accurate staging. 8 In one study, information necessary for surgical planning was missing in 85% of unstructured reports. Therefore, it is likely that some of the missing data from the ultrasound and initial CT or MRI examinations reports are simply omis- sions, rather than missed abnormalities. Despite these limitations the present study shows that ultrasoundandCT/MRI arecomplementary inthe evaluation of new renal tumours at diagnosis and that CT or MRI inev- itably adds crucial information, in addition tothe ultrasound ndings, to inform decision-making in these children. In conclusion, the ndings of the present study indicate that in just under half the patients CT or MRI added additional information in the local assessment of Wilms tumours at diagnosis, which may have inuenced the diagnostic pathway and treatment decisions. Sole reliance on ultrasound for Wilms staging risks missing signicant abnormalities. The information gained from cross-sectional imaging is likely to outweigh the risks due to radiation, sedation, or general anaesthetic. References 1. DAngio GJ. Pre- or postoperative therapy for Wilms tumour? J Clin Oncol 2008;25:4055e7. 2. Ehrlich PF. Wilms tumor: progress and considerations for the surgeon. Surg Oncol 2007;16:157e71. Figure 3 A 4-year-old female patient with large, right-sided renal tumour. Coronal, contrast-enhanced CT image of the chest and abdomen. There are multiple pulmonary metastases, and mediastinal lymph node enlargement. There is no clear fat plane between both the liver (large arrow) and abdominal wall (small arrow), and the large tumour arising from the upper pole of the right kidney. At surgery, adhesion to the liver and abdominal wall was conrmed. Figure 4 A 4-year-old male patient with large, right-sided mass. (a) Transverse ultrasound of the right upper quadrant showing the large heterogeneous mass, which displaces the liver, but a clear fat plane was difcult to demonstrate. (b) Contrast-enhanced axial CT image of the upper abdomen. A clear fat plane, suggesting no local invasion, is present between the large right-sided mass and the liver, which is displaced to the left. The ndings were conrmed at the time of surgery. K. McDonald et al. / Clinical Radiology 68 (2013) 16e20 19 3. Kaste SC, Dome JS, Babyn PS, et al. Wilms tumour: prognostic factors, staging, therapy and late effects. Pediatr Radiol 2008;38:2e17. 4. Brisse H, Smets AM, Kaste SC, et al. Imaging in unilateral Wilms tumour. Pediatr Radiol 2008;38:18e29. 5. Hoffer FA. Magnetic resonance imaging of abdominal masses in the pediatric patient. Semin Ultrasound, CT, MRI 2005;26:212e23. 6. Rohrschneider WK, Weirich A, Rieden K, et al. US, CT and MR imaging characteristics of nephroblastomatosis. Pediatr Radiol 1998;28:435e43. 7. Owens CM, Brisse HJ, Olsen OE, et al. Bilateral disease and new trends in Wilms tumour. Pediatr Radiol 2008;38:30e9. 8. Kee D, Zalcberg JR. Radiology reporting templates in oncology: a time for change. J Med Imaging Rad Oncol 2009;53:511e3. K. McDonald et al. / Clinical Radiology 68 (2013) 16e20 20
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