The Queensland Amyloidosis Centre is actively pursuing research to improve the diagnosis and management of patients with amyloidosis. Current research projects include:
- A study of the epidemiology of systemic amyloidosis in Queensland. This study will provide the first information on how common amyloidosis is in Australia.
- Fluorine-18-labelled florbetaben positron emission tomography to monitor cardiac amyloidosis. This study will see if PET scanning can be used to better monitor patients with cardiac amyloidosis.
- Improving diagnosis of amyloidosis by immunohistochemistry. A scientist from the Pathology Queensland PAH Anatomical Pathology laboratory has traveled to the UK National Amyloidosis Centre to bring back and improve local diagnsotic immunohistochemistry techniques.
- Sebia FLC assay for measuring serum free light chains in patients with AL amyloidosis. This study aims to see if a new way of measuring serum free light chains is better than existing tests.
- A Phase 3 Randomized, Controlled, Open-Label, Multicenter, Safety and Efficacy Study of Dexamethasone Plus MLN9708 or Physician’s Choice of Treatment Administered to Patients With Relapsed or Refractory Systemic Light-Chain (AL) Amyloidosis. This international study is testing wither a new drug called ixazomib (=MLN9708) is better than other standard treatments for patients with AL amyloidosis whose disease has not responded or come back after initial treatment.
- A Study to Evaluate the Efficacy and Safety of Daratumumab in Combination with Cyclophosphamide, Bortezomib and Dexamethasone (CyBorD) Compared with CyBorD alone in Newly Diagnosed Systemic Light-Chain (AL) Amyloidosis. This international study is testing whether a new drug called daratumumab can improve the outcome of newly diagnosed patients with AL amyloidosis when added to the standard chemotherapy regimen called CyBorD.
- Natural history of ATTRwt. The cardiology department is leading an Australian-wide study to better understand ATTRwt (=senile cardiac amyloidosis)
Publications.
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The treatment of paraprotein-related kidney disease. Hutchison CA, Xiong F, Mollee P. Curr Opin Nephrol Hypertens. 2017 Nov;26(6):477-483
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Mass spectrometry analysis for amyloidosis typing – is the future bright for its clinical implementation? Hill MM, Mollee PN. Expert Rev Proteomics. 2017 Jul;14(7):565-566
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Cardiac amyloid imaging with <sup>18</sup>F-florbetaben positron emission tomography: a pilot study. Law WP, Wang W, Moore P, Mollee P, Ng A. Amyloid. 2017 Mar;24(sup1):162
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Malabsorption Secondary to Gout-Induced Amyloidosis. Azzam A, Balasubramaniam R, Safa S, McIvor C, Mollee P. ACG Case Rep J. 2017 Mar 1;4:e32
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The Utility of 99mTc-DPD Scintigraphy in the Diagnosis of Cardiac Amyloidosis: An Australian Experience. Moore PT, Burrage MK, Mackenzie E, Law WP, Korczyk D, Mollee P. Heart Lung Circ. 2017 Nov;26(11):1183-1190
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Cardiac Amyloid Imaging with 18F-Florbetaben PET: A Pilot Study. Law WP, Wang WY, Moore PT, Mollee PN, Ng AC. J Nucl Med. 2016 Nov;57(11):1733-1739
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Implementation and evaluation of amyloidosis subtyping by laser-capture microdissection and tandem mass spectrometry. Mollee P, Boros S, Loo D, Ruelcke JE, Lakis VA, Cao KL, Renaut P, Hill MM. Clin Proteomics. 2016 Oct 27;13:3
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Free light chain testing for the diagnosis, monitoring and prognostication of AL amyloidosis. Mollee P, Merlini G. Clin Chem Lab Med. 2016 Jun 1;54(6):921-7
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Management of systemic AL amyloidosis: recommendations of the Myeloma Foundation of Australia Medical and Scientific Advisory Group. Weber N, Mollee P, Augustson B, Brown R, Catley L, Gibson J, Harrison S, Ho PJ, Horvath N, Jaksic W, Joshua D, Quach H, Roberts AW, Spencer A, Szer J, Talaulikar D, To B, Zannettino A, Prince HM. Intern Med J. 2015 Apr;45(4):371-82
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How to diagnose amyloidosis. Mollee P, Renaut P, Gottlieb D, Goodman H. Intern Med J. 2014 Jan;44(1):7-17
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Evaluation of the N Latex free light chain assay in the diagnosis and monitoring of AL amyloidosis. Mollee P, Tate J, Pretorius CJ. Clin Chem Lab Med. 2013 Dec;51(12):2303-10
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End-stage renal failure due to amyloidosis: outcomes in 490 ANZDATA registry cases. Tang W, McDonald SP, Hawley CM, Badve SV, Boudville N, Brown FG, Clayton PA, Campbell SB, de Zoysa JR, Johnson DW. Nephrol Dial Transplant. 2013 Feb;28(2):455-61
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A phase II study of risk-adapted intravenous melphalan in patients with AL amyloidosis. Mollee P, Tiley C, Cunningham I, Moore J, Prince HM, Cannell P, Gibbons S, Tate J, Paul S, Mar Fan H, Gill DS. Br J Haematol. 2012 Jun;157(6):766-9
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Proteomics in molecular diagnosis: typing of amyloidosis. Loo D, Mollee PN, Renaut P, Hill MM. J Biomed Biotechnol. 2011;2011:754109
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Current trends in the diagnosis, therapy and monitoring of the monoclonal gammopathies. Mollee P. Clin Biochem Rev. 2009 Aug;30(3):93-103
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Diagnostic and prognostic utility of the serum free light chain assay in patients with AL amyloidosis. Morris KL, Tate JR, Gill D, Kennedy G, Wellwood J, Marlton P, Bird R, Mills AK, Mollee P. Intern Med J. 2007 Jul;37(7):456-63
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Analytical performance of serum free light-chain assay during monitoring of patients with monoclonal light-chain diseases. Tate JR, Mollee P, Dimeski G, Carter AC, Gill D. Clin Chim Acta. 2007 Feb;376(1-2):30-6
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Hereditary fibrinogen A alpha-chain amyloidosis. Lane SW, Goodman HJ, Francis L, Bofinger A, Mollee PN. Pathology. 2006 Aug;38(4):380-2