Research Topics
Species | M MichaelSummaryAffiliation: Peter MacCallum Cancer Centre Country: Australia Publications
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Publications
A phase I trial of imatinib in combination with mFOLFOX6-bevacizumab in patients with advanced colorectal cancerM Michael
Division of Cancer Medicine, Peter MacCallum Cancer Centre, Locked Bag 1, A Beckett St, Victoria, 8006, Australia
Cancer Chemother Pharmacol 71:321-30. 2013..This phase I study aimed to assess the maximal tolerated dose (MTD) of imatinib in combination with mFOLFOX6-bevacizumab in patients with advanced colorectal cancer and to identify pharmacokinetic (PK) interactions and toxicities...
A multi-centre randomized, open-label phase II trial of continuous erlotinib plus gemcitabine or gemcitabine as first-line therapy in ECOG PS2 patients with advanced non-small cell lung cancerM Michael
Division of Hematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Australia
Oncol Rep 28:763-7. 2012..Erlotinib plus gemcitabine for the treatment of ECOG 2 NSCLC patients warrants further investigation including intermittent erlotinib regimens...
A phase I trial of Capecitabine+Gemcitabine with radical radiation for locally advanced pancreatic cancerM Michael
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Locked Bag 1, A Beckett Street, Melbourne, Victoria 8006, Australia
Br J Cancer 100:37-43. 2009..Dose level 2 was the recommend phase 2 dose. Disease control rate was 75%: PR=15%, SD=60%. Median overall survival was 11.2 months. The addition of Cap and Gem to radical RT was feasible and active and achieved at relatively low doses...
Tumoral drug metabolism: overview and its implications for cancer therapyM Michael
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Locked Bag 1, A Beckett St, Victoria 8006, Australia
J Clin Oncol 23:205-29. 2005..Only then can efforts be concentrated in the design of better prodrugs or combination therapy to improve drug efficacy and individualize therapy...
Drug metabolism by tumours: its nature, relevance and therapeutic implicationsMichael Michael
Peter MacCallum Cancer Centre, Division of Haematology and Medical Oncology, Locked Bag 1, A Beckett Street, Victoria, 8006, Australia
Expert Opin Drug Metab Toxicol 3:783-803. 2007..Only then can efforts be concentrated in the design of better prodrugs or combination therapy to optimise individual therapy...
A phase I trial of high-dose palliative radiotherapy plus concurrent weekly Vinorelbine and Cisplatin in patients with locally advanced and metastatic NSCLCM Michael
The Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Locked Bag 1, A Beckett St, Victoria 8006, Australia
Br J Cancer 93:652-61. 2005..This regimen was tolerable and produced meaningful responses for patients for whom locoregional control is required, but who are unsuitable for radical CRT...
Relationship of hepatic functional imaging to irinotecan pharmacokinetics and genetic parameters of drug eliminationMichael Michael
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Victoria, Australia
J Clin Oncol 24:4228-35. 2006....
Prognostic factors predictive of response and survival to a modified FOLFOX regimen: importance of an increased neutrophil countMichael Michael
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Victoria, 8006, Australia
Clin Colorectal Cancer 6:297-304. 2006..The aim of this study was to identify prognostic indicators of survival and response in a homogeneous population of chemotherapy-naive patients treated with oxaliplatin as part of 3 successive trials...
Open-label phase I trial of vandetanib in combination with mFOLFOX6 in patients with advanced colorectal cancerMichael Michael
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, St Andrews Place, East Melbourne, Victoria, 3002, Australia
Invest New Drugs 27:253-61. 2009..The safety and tolerability of vandetanib plus mFOLFOX6 was investigated in patients with advanced colorectal cancer (CRC)...
Docetaxel pharmacokinetics and its correlation with two in vivo probes for cytochrome P450 enzymes: the C(14)-erythromycin breath test and the antipyrine clearance testM Michael
Division of Cancer Medicine, Peter MacCallum Cancer Centre, Locked Bag 1, A Beckett St, Melbourne, VIC 8006, Australia
Cancer Chemother Pharmacol 69:125-35. 2012..This is the first report directly comparing the erythromycin breath test (EBT) (a CYP3A4 probe) with the antipyrine clearance test (ACT), (a general CYP-P450/predominant CYP3A4 probe) for the correlation with docetaxel PK and toxicity...
Phase II study of activated charcoal to prevent irinotecan-induced diarrheaMichael Michael
Department of Medical Oncology and Hematology, Princess Margaret Hospital, University of Toronto, Ontario, Canada
J Clin Oncol 22:4410-7. 2004..The aim of this study was to assess whether activated charcoal (AC), possibly by adsorbing free lumenal SN38, can reduce irinotecan-induced diarrhea (CID) and optimize its dose-intensity...
Phase Ib study of CP-868,596, a PDGFR inhibitor, combined with docetaxel with or without axitinib, a VEGFR inhibitorM Michael
Peter MacCallum Cancer Centre, Consultant Medical Oncologist, Division of Haematology and Medical Oncology, Chair of GI Clinical Service, Locked Bag 1, A Beckett Street, Victoria 8006, Australia
Br J Cancer 103:1554-61. 2010..Tumoural interstitial hypertension, possibly modulated by platelet-derived and vascular endothelial growth factor receptors (PDGFR and VEGFR), may mediate resistance to chemotherapy...
Oxaliplatin combined with infusional 5-fluorouracil and concomitant radiotherapy in inoperable and metastatic rectal cancer: a phase I trialS Loi
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, University of Melbourne, A Beckett Street, Melbourne, Victoria 8006, Australia
Br J Cancer 92:655-61. 2005..For future trials, oxaliplatin 85 mg m(-2) and 5-FU 200 mg m(-2) day(-1) continuous infusion 96 h week(-1) is the recommended dose when combined with 50.4 Gy of pelvic radiotherapy...
Phase I trial of docetaxel, cisplatin and concurrent radical radiotherapy in locally advanced oesophageal cancerF L Day
Department of Medical Oncology, Peter MacCallum Cancer Centre, Locked Bag 1, A Beckett St, Melbourne, Victoria 8006, Australia
Br J Cancer 104:265-71. 2011..The aim of this phase I trial was to assess the maximum tolerated dose (MTD) of a novel weekly docetaxel and cisplatin regimen concurrent with radical radiotherapy...
Phase I/II study of concurrent twice-weekly paclitaxel and weekly cisplatin with radiation therapy for stage III non-small cell lung cancerB Solomon
Peter MacCallum Cancer Institute, St. Andrews Place, East Melbourne, Vic. 3002, Australia
Lung Cancer 41:353-61. 2003..Paclitaxel can be safely given twice-weekly at a dose of 30 mg/m(2) in combination with weekly cisplatin (20 mg/m(2)) and thoracic RT (60 Gy), and this regimen has significant activity in stage III NSCLC...
A phase I/II trial of celecoxib with chemotherapy and radiotherapy in the treatment of patients with locally advanced oesophageal cancerS J Dawson
Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Locked Bag 1, A Beckett St, Victoria, 8006, Australia
Invest New Drugs 25:123-9. 2007..The study's aim was to determine the maximum tolerated dose (MTD) of celecoxib combined with chemoradiotherapy (CRT) for locally advanced oesophageal cancer (OC)...
A phase I trial of docetaxel and gemcitabine in patients with advanced cancerD Rischin
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Institute, Melbourne, Australia
Ann Oncol 11:421-6. 2000..Docetaxel and gemcitabine are active in a broad range of malignancies. The objective of this phase I trial was to determine the maximally tolerated doses of the combination of docetaxel and gemcitabine...
A phase I trial of preoperative radiotherapy and capecitabine for locally advanced, potentially resectable rectal cancerS Y K Ngan
Division of Radiation Oncology, Peter MacCallum Cancer Centre, St Andrews Place, East Melbourne, Victoria 3002, Australia
Br J Cancer 91:1019-24. 2004..4 Gy. For patients with resectable rectal cancer receiving concurrent, full dose radiotherapy, the recommended dose of capecitabine for further study is 1800 mg m(-2) day(-1) when given in this schedule...
FDG-PET metabolic response predicts outcomes in anal cancer managed with chemoradiotherapyF L Day
Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Locked Bag 1, A Beckett Street, Melbourne, 8006, Victoria, Australia
Br J Cancer 105:498-504. 2011..The aim was to investigate the correlation between (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) metabolic response to chemoradiotherapy and clinical outcomes in squamous cell carcinoma (SCC) of the anus...
Adjuvant and neoadjuvant therapy for gastric cancer using epirubicin/cisplatin/5-fluorouracil (ECF) and alternative regimens before and after chemoradiationT Leong
Peter MacCallum Cancer Centre, St Andrews Place, Melbourne, Victoria 3002, Australia
Br J Cancer 89:1433-8. 2003..Our results suggest that this adjuvant regimen can be delivered safely and with acceptable toxicity. This regimen forms the basis of several new studies being developed for postoperative adjuvant therapy of gastric cancer...
Metabolic response of rectal cancer assessed by 18-FDG PET following chemoradiotherapy is prognostic for patient outcomeJ M C Yeung
Department of Surgical Oncology, Peter MacCallum Cancer Centre, St Andrew s Place, East Melbourne, Victoria, Australia
Dis Colon Rectum 54:518-25. 2011..Sequential 18-FDG PET may be an early surrogate for pathological response to chemoradiotherapy...
The palliative benefit of irinotecan in 5-fluorouracil-refractory colorectal cancer: its prospective evaluation by a Multicenter Canadian TrialM Michael
Department of Hematology and Medical Oncology, Peter MacCallum Cancer Institute, Locked Bag 1, A Beckett St, Victoria, 8006, Australia
Clin Colorectal Cancer 2:93-101. 2002..2 months. Irinotecan provides a rate of palliative benefit higher than the radiological response rate. Patients-oriented palliative endpoints can be useful in assessing the benefit of agents in early-phase clinical trials...
Tumoral drug metabolism: perspectives and therapeutic implicationsM M Doherty
Department of Pharmaceutics, Victorian College of Pharmacy, Monash University, 381 Royal Parade, Parkville, 3052, Victoria, Australia
Curr Drug Metab 4:131-49. 2003..Various gene therapy approaches have been attempted experimentally with promising results. However, there are major gaps in understanding the implications of tumoral DME in disease progression (including metastasized tissue) and relapse...
Gastrointestinal stromal tumour treated with neoadjuvant imatinibM B Loughrey
Department of Pathology, Peter MacCallum Cancer Centre, Melbourne, VIC 3002, Australia
J Clin Pathol 58:779-81. 2005..The implications for this management option of radiological, pathological, and molecular assessment are discussed...
Phase I dose-finding and pharmacokinetic study of paclitaxel and carboplatin with oral valspodar in patients with advanced solid tumorsA Patnaik
Princess Margaret Hospital, Ontario Cancer Institute, Toronto, Canada
J Clin Oncol 18:3677-89. 2000....
Association of acquired Pelger-Huet anomaly with taxoid therapyS K Juneja
Department of Pathology, Peter MacCallum Cancer Institute, Melbourne, Australia
Br J Haematol 93:139-41. 1996..001) and for paclitaxel compared with controls (P = 0.007). We conclude that taxoid therapy produces transient APHA which peaks between days 3 and 9 and is more pronounced with docetaxel than with paclitaxel...
Beyond 5-fluorouracil: new horizons in systemic therapy for advanced colorectal cancerKenneth Khamly
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Victoria 8006, Australia
Expert Opin Investig Drugs 14:607-28. 2005..This paper reviews these and other advances in the care of patients with advanced colorectal cancer and discusses a number of agents that are currently under development...
Implications of dose rounding of chemotherapy to the nearest vial sizeMichael Joseph Dooley
Pharmacy Department, Peter MacCallum Cancer Centre, St Andrew s Place, 3002 East Melbourne, Australia
Support Care Cancer 12:653-6. 2004..The objective here was to explore the magnitude of the effect of dose rounding to the nearest whole vial strength for some newly marketed expensive cytotoxic chemotherapy agents...
A novel combination of cisplatin, irinotecan, and capecitabine in patients with advanced cancerMichael Jefford
Centre for Developmental Cancer Therapeutics, Melbourne, Victoria, Australia
Invest New Drugs 22:185-92. 2004..We conducted a dose escalation study combining cisplatin, irinotecan, and capecitabine (CIC), aiming to establish the maximum tolerated doses (MTD), side effect profile, and dose-limiting toxicity (DLT) of this novel regimen...
Adjuvant chemoradiation for gastric cancer using epirubicin, cisplatin, and 5-fluorouracil before and after three-dimensional conformal radiotherapy with concurrent infusional 5-fluorouracil: a multicenter study of the Trans-Tasman Radiation Oncology GrouTrevor Leong
Division of Radiation Oncology, Department of Radiation Therapy Services, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
Int J Radiat Oncol Biol Phys 79:690-5. 2011..We conducted a prospective, multicenter study to evaluate an alternative chemoradiation regimen that combines more current systemic treatment with modern techniques of radiotherapy delivery...
A pilot human evaluation of a formulation of irinotecan and hyaluronic acid in 5-fluorouracil-refractory metastatic colorectal cancer patientsPeter Gibbs
Department of Medical Oncology and Haematology, Royal Melbourne Hospital, Melbourne, Australia
Chemotherapy 55:49-59. 2009..This study was designed as a first-in-man investigation of the safety and pharmacokinetics of irinotecan when administered within the HA-Irinotecan formulation...
A randomized cross-over trial to determine the effect of Cremophor EL on the pharmacodynamics and pharmacokinetics of carboplatin chemotherapySherene Loi
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia
Cancer Chemother Pharmacol 54:407-14. 2004..CONCLUSION: CrEL at this dose and schedule does not appear to be a major contributory factor to the platelet-sparing effect of paclitaxel when combined with carboplatin, nor does it alter the pharmacokinetics of carboplatin...
Long-term survival following chemoradiation for inoperable non-small cell lung cancerNikki M Plumridge
Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Vic, Australia
Med J Aust 189:557-9. 2008..To measure long-term survival following combined chemotherapy and radiotherapy for inoperable non-small cell lung cancer...
Part I: Liver function in oncology: biochemistry and beyondKathryn M Field
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Locked Bag 1, Vic, Australia
Lancet Oncol 9:1092-101. 2008....
177Lu-octreotate, alone or with radiosensitising chemotherapy, is safe in neuroendocrine tumour patients previously treated with high-activity 111In-octreotideDaniel Hubble
Centre for Molecular Imaging, Peter MacCallum Cancer Centre, 12 St Andrew s Place, East Melbourne, VIC 3002, Australia
Eur J Nucl Med Mol Imaging 37:1869-75. 2010....
Complete radiological and metabolic response of metastatic renal cell carcinoma to SU5416 (semaxanib) in a patient with probable von Hippel-Lindau syndromeRoss R Jennens
Department of Medical Oncology, Royal Melbourne Hospital, Parkville, Victoria, Australia
Urol Oncol 22:193-6. 2004..While vascular endothelial growth factor (VEGF) inhibitors have been shown to produce a modest response in sporadic metastatic RCC, further studies utilizing VEGF inhibitors in patients with VHL syndrome and RCC warrants exploration...
Local control and survival following concomitant chemoradiotherapy in inoperable stage I non-small-cell lung cancerMarie Pierre Campeau
Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
Int J Radiat Oncol Biol Phys 74:1371-5. 2009..The effect of CRT on local control in Stage I NSCLC is less well documented. We retrospectively reviewed local control and survival following CRT or RT for inoperable Stage I NSCLC patients...
Impact of positron emission tomography on the management of patients with small-cell lung cancer: preliminary experienceRobert Blum
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Institute, East Melbourne, Vic, Australia
Am J Clin Oncol 27:164-71. 2004..PET-CR conferred longer median time to progression (13.7 months) than no CR (9.7 months). FDG-PET for SCLC was often discordant with conventional assessment and frequently influenced management...
Part II: Liver function in oncology: towards safer chemotherapy useKathryn M Field
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Vic, Australia
Lancet Oncol 9:1181-90. 2008..Furthermore, we review other assessments of liver metabolic and excretory function, particularly in the setting of chemotherapy drug handling. We discuss the potential use of these metabolic probes in practice...
Role of xenobiotic metabolic enzymes in cancer epidemiologyMadhu S Singh
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Victoria, Australia
Methods Mol Biol 472:243-64. 2009..The data may have relevance in one population but not for another for a specific malignancy and at times may be conflicting. We believe that with mature data in the future it may be possible to stratify patients by risk...
The Lewis-Y carbohydrate antigen is expressed by many human tumors and can serve as a target for genetically redirected T cells despite the presence of soluble antigen in serumJennifer A Westwood
Cancer Immunology Research Program, Peter MacCallum Cancer Centre, St Andrews Place, Melbourne, Victoria 3002, Australia
J Immunother 32:292-301. 2009....
FDG-PET status following chemoradiotherapy provides high management impact and powerful prognostic stratification in oesophageal cancerCuong P Duong
Division of Surgical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
Eur J Nucl Med Mol Imaging 33:770-8. 2006..CMR status as assessed by PET powerfully stratified prognosis. Even in the absence of a baseline study, normalisation of uptake at all sites of known tumoral involvement carries a good medium-term prognosis...
Locally advanced and metastatic gastric cancer: current management and new treatment developmentsKathryn Field
Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
Drugs 68:299-317. 2008..Overall, there remains optimism that further incremental gains will be achieved with future studies combining chemotherapy, radiotherapy and targeted therapies, both in the adjuvant and metastatic disease settings...
Adjuvant therapy in gastric cancerLionel Lim
Peter MacCallum Cancer Centre, East Melbourne, Victoria 3002, Australia
J Clin Oncol 23:6220-32. 2005..Issues such as the identification of patients who are more likely to benefit from adjuvant therapy are also addressed. Further clinical trials are needed to move towards better consensus and standardization of care...
Recent developments in the systemic therapy of advanced gastroesophageal malignanciesKenneth Khamly
Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Victoria 8006, Australia
Expert Opin Investig Drugs 15:131-53. 2006..This article reviews the current clinical data regarding systemic therapy for patients with advanced upper gastrointestinal malignancies...
Tolerability of accelerated chest irradiation and impact on survival of prophylactic cranial irradiation in patients with limited-stage small cell lung cancer: review of a single institution's experienceMichael Ng
Department of Radiation Oncology, Peter MacCallum Cancer Centre, East Melbourne, Australia
J Thorac Oncol 2:506-13. 2007..We have reviewed the experience at Peter MacCallum Cancer Centre to determine the tolerability of these treatments in routine practice and to determine their effects on survival...
Modification of leucovorin dose within a simplified FOLFOX regimen improves tolerability without compromising efficacyStephen Clarke
Department of Medical Oncology, Royal Prince Alfred Hospital Sydney Cancer Centre, Sydney, Australia
Clin Colorectal Cancer 6:578-82. 2007..This analysis assesses the efficacy and safety of a modified FOLFOX (oxaliplatin/leucovorin [LV]/5-fluorouracil [5-FU]) regimen given with a low dose of LV...
FDG-PET-detected extracranial metastasis in patients with non-small cell lung cancer undergoing staging for surgery or radical radiotherapy--survival correlates with metastatic disease burdenMichael R MacManus
Department of Radiation Oncology, Peter MacCallum Cancer Institute, Melbourne, Victoria, Australia
Acta Oncol 42:48-54. 2003..027) but not pre-PET stage, weight loss or metastasis site correlated with survival. PET-detected metastatic tumor burden appeared to influence survival and should be evaluated as a prognostic factor in NSCLC...
Addition of gabapentin to a modified FOLFOX regimen does not reduce oxaliplatin-induced neurotoxicityPaul L Mitchell
Austin Hospital, Heidelberg, Melbourne, Australia E mail
Clin Colorectal Cancer 6:146-51. 2006..Sensory neurotoxicity is dose limiting for oxaliplatin, an effective drug in the treatment of colorectal cancer (CRC) and other malignancies. This study assessed the impact of gabapentin on oxaliplatin dose intensity and neurotoxicity...
A randomized, double-blinded, placebo-controlled phase II trial of recombinant human leukemia inhibitory factor (rhuLIF, emfilermin, AM424) to prevent chemotherapy-induced peripheral neuropathyIan D Davis
Austin Health, Studley Road, Heidelberg, Victoria 3084, Australia
Clin Cancer Res 11:1890-8. 2005....
Expression and prognostic significance of kit, protein kinase B, and mitogen-activated protein kinase in patients with small cell lung cancerFiona H Blackhall
Department of Medical Oncology, University Health Network-Princess Margaret Hospital, University of Toronto, Toronto, Ontario, M5G 2M5 Canada
Clin Cancer Res 9:2241-7. 2003..8 years for positive staining; P = 0.0054). CONCLUSIONS: Kit, PKB/Akt, and MAPK are expressed in a high percentage of SCLCs, and our data suggest that MAPK is an independent positive predictive factor in this malignancy...
