369 results match your criteria: "National Health and Medical Research Council Clinical Trials Centre[Affiliation]"
Br J Cancer
February 2014
Research and Development, Bristol-Myers Squibb, 100 Nassau Park Boulevard, Princeton, NJ 08540, USA.
Background: Anti-EGFR antibody, cetuximab, improves overall survival (OS) in K-ras wild-type chemotherapy-refractory colorectal cancer. Epidermal growth factor receptor ligand epiregulin (EREG) gene expression may further predict cetuximab benefit.
Methods: Tumour samples from a phase III clinical trial of cetuximab plus best supportive care (BSC) vs BSC alone (CO.
Oncologist
October 2014
Australian and New Zealand Gynaecological Oncology Group and National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, Australia;
Chemotherapy for platinum-resistant/refractory ovarian cancer is motivated by the hope of benefit. We sought to determine the relationships between: (a) trait hope, expectation of symptom benefit from chemotherapy, and anxiety and depression; (b) hope and perceived efficacy of chemotherapy; and (c) unfulfilled hope (where expectations for benefit are not fulfilled) and depression. Methods.
View Article and Find Full Text PDFJ Clin Oncol
October 2013
Belinda E. Kiely, Andrew J. Martin, and Martin R. Stockler, National Health and Medical Research Council Clinical Trials Centre, University of Sydney; Belinda E. Kiely, Martin H.N. Tattersall, Nicholas R.C. Wilcken, Philip J. Beale, and Martin R. Stockler, Sydney Medical School, University of Sydney; Belinda E. Kiely, Martin H.N. Tattersall, Philip J. Beale, and Martin R. Stockler, Sydney Cancer Centre-Royal Prince Alfred and Concord Hospitals, Sydney; David Goldstein, Prince of Wales Hospital Clinical School, University of New South Wales, Kensington; Nicholas R.C. Wilcken, Westmead Hospital, Westmead; Ehtesham A. Abdi, Tweed Hospital, Tweed Heads; Amanda Glasgow, Wollongong Hospital, Wollongong, New South Wales; Anna K. Nowak, School of Medicine and Pharmacology, University of Western Australia, Crawley; Anna K. Nowak, Sir Charles Gardner Hospital, Nedlands, Western Australia; David K. Wyld, Royal Brisbane and Women's Hospital, Brisbane, Queensland; Michael Jefford, Peter MacCallum Cancer Centre; Michael Jefford, University of Melbourne, Melbourne, Victoria, Australia; and Paul A. Glare, Memorial Sloan-Kettering Cancer Center, New York, NY.
Purpose: To determine the accuracy and usefulness of oncologists' estimates of survival time in individual patients with advanced cancer.
Patients And Methods: Twenty-one oncologists estimated the "median survival of a group of identical patients" for each of 114 patients with advanced cancer. Accuracy was defined by the proportions of patients with an observed survival time bounded by prespecified multiples of their estimated survival time.
Pediatr Res
December 2013
1] Newborn Care, Royal Prince Alfred Hospital, Sydney, Australia [2] Sydney School of Public Health, University of Sydney, Sydney, Australia.
Background: Undernutrition in neonates increases the risk of serious morbidities. The objective of this study was to describe neonatal morbidity associated with low body fat percentage (BF%) and measure the number of undernourished neonates defined by BF% and compare this with birth weight percentiles (<10th).
Methods: Eligibility included term (≥37 wk) neonates.
Asia Pac J Clin Oncol
June 2014
National Health and Medical Research Council Clinical Trials Centre, University of Sydney.
Aims: To provide data on the patterns of care in neuro-oncology practices at Australian cancer centres over the previous 12-month period.
Methods: A 5-page questionnaire was sent to Cooperative Trials Group for Neuro-Oncology members at 28 Australia cancer centres. The questions included access to neuro-oncology services; treatment protocols and patterns of supportive care.
Obstet Gynecol
April 2013
Gynaecological Cancer Centre, The Royal Hospital for Women, the School of Women's and Children's Health and the Department of Medicine, Clinical School, University of New South Wales, and the Department of Radiation Oncology, Prince of Wales Hospital, Randwick, the Hunter Area Pathology Service, Faculty of Health Sciences, University of Newcastle, Newcastle, and the National Health and Medical Research Council Clinical Trials Centre, the University of Sydney, Camperdown, New South Wales, Australia.
Objective: To examine the outcome for patients with stage IB2 cervical cancer treated primarily with radical hysterectomy, and to determine the need for adjuvant therapy, the sites of recurrence, and the morbidity of the treatment.
Methods: We reviewed our experience with 93 patients with stage IB2 cervical cancer treated with primary surgery at the Royal Hospital for Women in Sydney from 1988 to 2008. All patients underwent radical hysterectomy and pelvic lymphadenectomy.
J Natl Cancer Inst
May 2013
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, Australia.
Background: The epidermal growth factor receptor (EGFR) signaling pathway is crucial for regulating tumorigenesis and cell survival and may be important in the development and progression of non-small cell lung cancer (NSCLC). We examined the impact of EGFR-tyrosine kinase inhibitors (TKIs) on progression-free survival (PFS) and overall survival (OS) in advanced NSCLC patients with and without EGFR mutations.
Methods: Randomized trials that compared EGFR-TKIs monotherapy or combination EGFR-TKIs-chemotherapy with chemotherapy or placebo were included.
BJU Int
May 2013
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, NSW, Australia.
Unlabelled: WHAT'S KNOWN ON THE SUBJECT? AND WHAT DOES THE STUDY ADD?: Non-muscle-invasive bladder cancer has a significant recurrence and progression rate despite transurethral resection. The current standard of care to lower the risk of recurrence and progression is adjuvant BCG followed by maintenance BCG. Despite this, a significant number of patients experience recurrence and progress to invasive cancer.
View Article and Find Full Text PDFMed J Aust
June 2012
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, NSW.
Objectives: To estimate the incidence of metastatic breast cancer (MBC) in Australian women with an initial diagnosis of non-metastatic breast cancer.
Design, Setting And Participants: A population-based cohort study of all women with non-metastatic breast cancer registered on the New South Wales Central Cancer Register (CCR) in 2001 and 2002 who received care in a NSW hospital.
Main Outcome Measures: 5-year cumulative incidence of MBC; prognostic factors for MBC.
Lung Cancer
September 2012
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Locked Bag 77, Camperdown, NSW 1450, Australia.
Introduction: We sought to estimate life expectancy scenarios for patients starting chemotherapy for advanced non-small-cell lung cancer (NSCLC).
Methods: We searched for randomized first-line chemotherapy trials published from January 2000 to April 2008. We recorded median time to progression (TTP) and median overall survival (OS) and extracted the following percentiles (represented scenario) from each OS curve: 90th (worst-case), 75th (lower-typical), 25th (upper-typical) and 10th (best-case).
Ann Oncol
August 2012
Department of Oncology, Hôpital Hôtel-Dieu, Paris, France.
Background: In the CALYPSO trial, carboplatin-pegylated liposomal doxorubicin (CD) demonstrated superior therapeutic index versus carboplatin-paclitaxel (CP) in patients with recurrent ovarian cancer. This paper reports the health-related quality of life (HRQoL) findings.
Materials And Methods: HRQoL was measured with the EORTC QoL-QC30 questionnaire and OV28 ovarian cancer module.
J Oncol Pract
September 2011
Duke Comprehensive Cancer Center; Department of Surgery; Department of Medicine, Division of Medical Oncology, Duke University Medical Center, Durham NC; Discipline of Palliative and Supportive Services; Department of Medical Oncology, Flinders Medical Centre, Flinders University, Adelaide; National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Camperdown; Sydney Cancer Centre, Royal Prince Alfred and Concord Hospitals, Sydney, Australia; Allama Iqbal Medical College, Lahore, Pakistan; Department of Medical Oncology, Tata Memorial Hospital, Mumbai, India; NCIC Clinical Trials Group, Kingston, Ontario, Canada.
Purpose: To understand the diversity of issues and the breadth of growing clinical care, professional education, and clinical research needs of developing countries, not typically represented in Western or European surveys of cancer care and research.
Methods: A cross-sectional survey was conducted of the attendees at the 2010 Australia and Asia Pacific Clinical Oncology Research Development workshop (Queensland, Australia) about the most important health care questions facing the participant's home countries, especially concerning cancer.
Results: Early-career oncologists and advanced oncology trainees from a region of the world containing significant low- and middle-income countries reported that cancer is an emerging health priority as a result of aging of the population, the impact of diet and lifestyle, and environmental pollution.
Diabetes Care
February 2012
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, New South Wales, Australia.
Objective: Diabetic patients with moderate renal impairment (estimated glomerular filtration rate [eGFR] 30-59 mL/min/1.73 m(2)) are at particular cardiovascular risk. Fenofibrate's safety in these patients is an issue because it may elevate plasma creatinine.
View Article and Find Full Text PDFDev Med Child Neurol
March 2012
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, Australia.
Aim: The collection of data on longer-term neurodevelopmental outcomes within large neonatal randomized controlled trials by trained assessors can greatly increase costs and present many operational difficulties. The aim of this study was to develop a more practical alternative for identifying major cognitive delay in infants at the age of 24 months, based on parental reports.
Method: A sample of 476 infants (206 female, 270 male) previously diagnosed with neonatal sepsis (mean birthweight 1329g [SD 865g], mean gestational age at birth 28.
J Clin Oncol
December 2011
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Locked Bag 77, Camperdown, NSW 1450, Australia.
Purpose: We compared oral capecitabine, administered intermittently or continuously, versus classical cyclophosphamide, methotrexate, and fluorouracil (CMF) as first-line chemotherapy for women with advanced breast cancer unsuited to more intensive regimens.
Patients And Methods: Three hundred twenty-three eligible women were randomly assigned to capecitabine administered intermittently (1,000 mg/m(2) twice daily for 14 of every 21 days; n = 107) or continuously (650 mg/m(2) twice daily for 21 of every 21 days; n = 107), or to classical CMF (oral cyclophosphamide 100 mg/m(2) days 1 to 14 with intravenous methotrexate 40 mg/m(2) and fluorouracil 600 mg/m(2) on days 1 and 8 every 28 days; n = 109). The primary end point was quality-adjusted progression-free survival (PFS); secondary end points included PFS, overall survival (OS), objective tumor response, and adverse events.
Pediatrics
October 2011
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, Australia.
Background: Inhaled nitric oxide (iNO) is an effective therapy for pulmonary hypertension and hypoxic respiratory failure in term infants. Fourteen randomized controlled trials (n = 3430 infants) have been conducted on preterm infants at risk for chronic lung disease (CLD). The study results seem contradictory.
View Article and Find Full Text PDFBiostatistics
January 2012
Department of Statistics, Macquarie University, NSW 2109, Australia and National Health and Medical Research Council Clinical Trials Centre, University of Sydney, NSW 2006, Australia.
Relative risks (RRs) are generally considered preferable to odds ratios in prospective studies. However, unlike logistic regression for odds ratios, the standard log-binomial model for RR regression does not respect the natural parameter constraints and is therefore often subject to numerical instability. In this paper, we develop a reliable and flexible method for fitting log-binomial models.
View Article and Find Full Text PDFBMJ
September 2011
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, 92-94 Parramatta Road, Locked Bag 77, Camperdown NSW 2050, Australia.
Oncologist
February 2012
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, NSW, Australia.
The results of quality of life analyses from a randomized, placebo-controlled phase III trial of everolimus for metastatic renal cell carcinoma patients progressing after treatment with sunitinib or sorafenib are reviewed.
View Article and Find Full Text PDFLancet Oncol
July 2011
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, NSW, Australia.
Background: In a previous meta-analysis, we identified a survival benefit from neoadjuvant chemotherapy or chemoradiotherapy before surgery in patients with resectable oesophageal carcinoma. We updated this meta-analysis with results from new or updated randomised trials presented in the past 3 years. We also compared the benefits of preoperative neoadjuvant chemotherapy compared with neoadjuvant chemoradiotherapy.
View Article and Find Full Text PDFAnn Oncol
November 2011
University Paris Descartes, AP-HP, Hôpitaux Universitaires Paris Centre site Hôtel-Dieu, France.
Background: CALYPSO (CAeLYx in Platinum Sensitive Ovarian) patients compared carboplatin-pegylated liposomal doxorubicin (C-PLD) with carboplatin-paclitaxel (C-P) in patients with late-relapsing recurrent ovarian cancer (ROC). We analyzed outcomes in patients ≥70 years.
Patients And Methods: Nine hundred and seventy-six patients with taxane-pretreated ROC relapsing >6 months after first- or second-line platinum-based therapy were randomly assigned to 4-weekly C area under the curve (AUC) 5 plus PLD 30 mg/m(2) or 3-weekly C AUC 5 plus P 175 mg/m(2) for six or more cycles.
J Clin Oncol
February 2011
National Health and Medical Research Council Clinical Trials Centre and Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
Purpose: To estimate scenarios for survival for women with metastatic breast cancer (MBC) who are starting chemotherapy.
Patients And Methods: We sought randomized, first-line chemotherapy trials for MBC published from 1999 to 2009. We recorded median progression-free survival (PFS) and median overall survival (OS) and extracted the following percentiles (represented scenario) from each OS curve: 90th (worst-case), 75th (lower-typical), 25th (upper-typical), and 10th (best-case).
J Clin Oncol
June 2010
National Health and Medical Research Council Clinical Trials Centre, Camperdown, New South Wales 1450, Australia.
PLoS One
January 2010
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, Australia.
Background: When rates of uptake of other drugs differ between treatment arms in long-term trials, the true benefit or harm of the treatment may be underestimated. Methods to allow for such contamination have often been limited by failing to preserve the randomization comparisons. In the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study, patients were randomized to fenofibrate or placebo, but during the trial many started additional drugs, particularly statins, more so in the placebo group.
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