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Dive into the research topics where Amanda J. Byrne is active.

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Featured researches published by Amanda J. Byrne.


The Journal of Nuclear Medicine | 2008

PET Changes Management and Improves Prognostic Stratification in Patients with Recurrent Colorectal Cancer: Results of a Multicenter Prospective Study

Andrew M. Scott; Dishan H. Gunawardana; Ben Kelley; John Stuckey; Amanda J. Byrne; Jayne Ramshaw; Michael J. Fulham

The aims of our study were to examine the impact of PET in changing management in patients with proven or suspected colorectal cancer recurrence and to assess the impact of management change on disease-free survival. Methods: Symptomatic patients with a residual structural lesion suggestive of recurrent tumor (group A) or patients with pulmonary or hepatic metastases considered to be potentially resectable (group B) underwent PET scans. Pre-PET management plans were documented by referring clinicians unaware of the PET results, and follow-up to 12 mo was performed to determine actual management and clinical outcomes. Results: A total of 191 patients (118 men and 73 women; mean age, 66 y) were studied. PET detected additional sites of disease in 48.4% of patients in group A and in 43.9% of patients in group B. A change in planned management was documented in 65.6% of group A and in 49.0% of group B patients. These management plans were implemented in 96% of patients. Follow-up data in group A showed progressive disease in 60.5% of patients with additional lesions detected by PET, compared with conventional imaging, and in 36.2% of patients with no additional lesions detected by PET (P = 0.04). In group B, progressive disease was identified in 65.9% of patients with additional lesions detected by PET and in 39.2% of patients with no additional lesions detected by PET (P = 0.01). PET also provided valuable prognostic information on patients stratified into curative- or palliative-intent groups. Conclusion: These data demonstrate the significant impact of PET on management and outcomes in patients with suspected recurrent colorectal cancer.


European Journal of Nuclear Medicine and Molecular Imaging | 2005

Assessment of the role of FDG PET in the diagnosis and management of children with refractory epilepsy

Glenn P. Ollenberger; Amanda J. Byrne; Salvatore U. Berlangieri; Christopher C. Rowe; Kunthi Pathmaraj; David C. Reutens; Samuel F. Berkovic; Ingrid E. Scheffer; Andrew M. Scott

PurposeWe performed a retrospective analysis of the results of FDG PET scans in children with refractory epilepsy referred to our centre over an 8-year period, with a view to ascertaining the impact of FDG PET on subsequent patient management.MethodsA questionnaire was used to assess the impact of FDG PET scan on diagnosis, management and clinical decision-making processes for epilepsy surgery from the managing clinician’s perspective. FDG PET scan results were also compared with MRI, EEG and SPECT results and coded according to whether the FDG PET scan provided independent information and localisation of epileptogenic regions.ResultsA total of 118 eligible patients under the age of 14 years were identified, with questionnaires being completed on 113 evaluable patients (96%). The pre-PET management plan consisted of consideration for surgery in 92 patients (81%) and medical therapy for the remaining 21 patients (19%). Managing physicians rated FDG PET as providing information additional to that obtained with other investigations regarding epileptogenic sites in 88 patients (77%). FDG PET had either a minor or a major impact on clinical management in 58 patients (51%), principally with regard to surgical candidacy.ConclusionFDG PET has a definite role in the assessment of paediatric patients with refractory epilepsy who are being considered for surgery. In the future, analysis of FDG PET data in specific subpopulations of children with refractory epilepsy may lead to novel insights regarding aetiology.


European Journal of Nuclear Medicine and Molecular Imaging | 2005

Positron emission tomography with selected mediastinoscopy compared to routine mediastinoscopy offers cost and clinical outcome benefits for pre-operative staging of non-small cell lung cancer

Kelvin K. Yap; Kenneth S. K. Yap; Amanda J. Byrne; Salvatore U. Berlangieri; Aurora Poon; Paul Mitchell; Simon Knight; Peter C. Clarke; Anthony Harris; Andrew Tauro; Christopher C. Rowe; Andrew M. Scott

Purpose18F-fluorodeoxyglucose positron emission tomography (FDG-PET) imaging is an important staging procedure in patients with non-small cell lung cancer (NSCLC). We aimed to demonstrate, through a decision tree model and the incorporation of real costs of each component, that routine FDG-PET imaging as a prelude to curative surgery will reduce requirements for routine mediastinoscopy and overall hospital costs.MethodsA decision tree model comparing routine whole-body FDG-PET imaging to routine staging mediastinoscopy was used, with baseline variables of sensitivity, specificity and prevalence of non-operable and metastatic disease obtained from institutional data and a literature review. Costings for hospital admissions for mediastinoscopy and thoracotomy of actual patients with NSCLC were determined. The overall and average cost of managing patients was then calculated over a range of FDG-PET costs to derive projected cost savings to the community.ResultsThe prevalence of histologically proven mediastinal involvement in patients with NSCLC presenting for surgical assessment at our institution is 20%, and the prevalence of distant metastatic disease is 6%. Based on literature review, the pooled sensitivity and specificity of FDG-PET for detection of mediastinal spread are 84% and 89% respectively, and for mediastinoscopy, 81% and 100%. The average cost of mediastinoscopy for NSCLC in our institution is AUD


Molecular Imaging and Biology | 2008

Role of Low-dose, Noncontrast Computed Tomography from Integrated Positron Emission Tomography/Computed Tomography in Evaluating Incidental 2-Deoxy-2-[F-18]fluoro-d-glucose-avid Colon Lesions

Sze Ting Lee; T. Tan; Aurora Poon; H. B. Toh; S. Gill; S. U. Berlangieri; E. Kraft; Amanda J. Byrne; Kunthi Pathmaraj; G. J. O’Keefe; Niall C. Tebbutt; Andrew M. Scott

4,160, while that of thoracotomy is AUD


Anz Journal of Surgery | 2012

Impact of ¹⁸F-FDG-PET in decision making for liver metastectomy of colorectal cancer.

Andrew McLeish; Sze Ting Lee; Amanda J. Byrne; Andrew M. Scott

15,642. The cost of an FDG-PET scan is estimated to be AUD


Molecular Imaging and Biology | 2009

Prognostic Value of 18F-FDG PET/CT in Patients with Malignant Pleural Mesothelioma

Sze Ting Lee; M. Ghanem; Rebecca A. Herbertson; S. U. Berlangieri; Amanda J. Byrne; K. Tabone; Paul Mitchell; Simon R. Knight; M. Feigen; Andrew M. Scott

1,500. Using these figures and the decision tree model, the average cost saving is AUD


Molecular Imaging and Biology | 2009

Prognostic Value of 18 F-FDG PET/CT in Patients with Malignant Pleural Mesothelioma

Sze Ting Lee; M. Ghanem; Rebecca A. Herbertson; S. U. Berlangieri; Amanda J. Byrne; K. Tabone; Paul Mitchell; Simon R. Knight; M. Feigen; Andrew M. Scott

2,128 per patient.ConclusionRoutine FDG-PET scanning with selective mediastinoscopy will save AUD


Asia Oceania journal of nuclear medicine & biology | 2014

In vivo imaging of cellular proliferation in renal cell carcinoma using 18F-fluorothymidine PET

Peter K. Wong; Sze Ting Lee; Carmel Murone; John Eng; Nathan Lawrentschuk; Salvatore U. Berlangieri; Kunthi Pathmaraj; Graeme O'Keefe; John Sachinidis; Amanda J. Byrne; Damien Bolton; Ian D. Davis; Andrew M. Scott

2,128 per patient and will potentially reduce inappropriate surgery. These cost savings remain robust over a wide range of disease prevalence and FDG-PET costs.


Molecular Imaging and Biology | 2009

Prognostic Value of 18

Sze-Ting Lee; M. Ghanem; Rebecca A. Herbertson; S. U. Berlangieri; Amanda J. Byrne; K. Tabone; Paul Mitchell; Simon R. Knight; M. Feigen; Andrew M. Scott

PurposeTo assess the contribution of concurrent low-dose, noncontrast CT in the assessment of the malignant potential of incidental focal 2-deoxy-2-[F-18]fluoro-d-glucose (FDG)-avid colonic lesions on positron emission tomography/computed tomography (PET/CT).ProceduresRoutine FDG-PET/CT scans were reviewed for identification of focal FDG-avid colon lesions, and the CT component was independently reviewed for an anatomical lesion and malignant potential based on CT criteria. Clinical, endoscopic, and histopathology follow-up was obtained.ResultsA total of 85/2,916 (3%) oncology FDG-PET/CT scans had incidental focal colon lesions. Clinical and/or endoscopic follow-up was available in 83/85 (98%) patients. Focal, corresponding CT lesions were found in 44/83 (53%) patients, but features of malignancy were not assessable. Of the 44 patients with a final diagnosis, 32/44 (73%) were FDG-PET/CT true positives; 5/44 (11%) were false positives; and 7/44 (16%) had inconclusive FDG-PET/CT findings.ConclusionsConcurrent low-dose, noncontrast CT improves localization, but does not provide independent information on the malignant potential of incidental focal colonic activity on FDG-PET/CT.


Molecular Imaging and Biology | 2008

Role of Low-dose, Noncontrast Computed Tomography from Integrated Positron Emission Tomography/Computed Tomography in Evaluating Incidental

Sze-Ting Lee; T. Tan; Aurora Poon; H. B. Toh; Sharlene Gill; S. U. Berlangieri; E. Kraft; Amanda J. Byrne; Kunthi Pathmaraj; Niall C. Tebbutt; Andrew M. Scott

Background:  The ability of 18F‐fluorodeoxyglucose positron emission tomography (FDG‐PET) to impact on management of patients with recurrent colorectal cancer is high. However, direct impact of FDG‐PET on surgical management of patients with potentially resectable hepatic metastases is limited.

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Sze Ting Lee

Ludwig Institute for Cancer Research

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S. U. Berlangieri

Ludwig Institute for Cancer Research

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Aurora Poon

Ludwig Institute for Cancer Research

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K. Tabone

Ludwig Institute for Cancer Research

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Rebecca A. Herbertson

Ludwig Institute for Cancer Research

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Simon R. Knight

Royal College of Surgeons of England

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