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1.
Asia Pac J Clin Oncol ; 13(2): e31-e40, 2017 Apr.
Article in English | MEDLINE | ID: mdl-27558311

ABSTRACT

AIM: We examined how sociodemographic, clinical and area-level factors are related to short-term prostate cancer mortality versus mortality from other causes, a crucial distinction for this disease that disproportionately affects men older than 60 years. METHODS: We applied competing risk survival models to administrative data from the Queensland Cancer Registry (Australia) for men diagnosed with prostate cancer between January 2005 and July 2007, including stratification by Gleason score. RESULTS: The men (n = 7393) in the study cohort had a median follow-up of 5 years 3 months. After adjustment, remoteness and area-level disadvantage were not significantly associated with prostate cancer mortality. However, area-level disadvantage had a significant negative relationship with hazard of death from a cause other than prostate cancer within 7 years; compared with those living in the most advantaged areas, the likelihood of mortality was higher for those in the most disadvantaged (subhazard ratio [SHR] = 1.39; 95% CI, 1.01-1.90; P = 0.041), disadvantaged (SHR = 1.51; 95% CI, 1.14-2.00; P = 0.004), middle (SHR = 1.34; 95% CI, 1.02-1.75; P = 0.034) and advantaged areas (SHR = 1.44; 95% CI, 1.09-1.89; P = 0.009). Those with Gleason score of 7 and higher had a lower hazard of prostate cancer mortality if they were living with a partner, whereas those with lower Gleason scores and living a partner had lower hazards of other-cause mortality. CONCLUSIONS: Understanding why men living in more disadvantaged areas have higher risk of non-prostate cancer mortality should be a priority.


Subject(s)
Prostatic Neoplasms/mortality , Aged , Cause of Death , Cohort Studies , Health Status Disparities , Humans , Male , Middle Aged , Neoplasm Grading , Prostatic Neoplasms/economics , Prostatic Neoplasms/pathology , Queensland/epidemiology , Registries , Risk Assessment , Risk Factors , Rural Population/statistics & numerical data , Social Class , Socioeconomic Factors
2.
Asian Pac J Cancer Prev ; 14(4): 2621-6, 2013.
Article in English | MEDLINE | ID: mdl-23725185

ABSTRACT

BACKGROUND: To review the peer reviewed literature on the psychological aspects of the prostate cancer experience of men in Asia. MATERIALS AND METHODS: Medline and PsycINFO, CINAHL, ProQuest, and Web of Science (1999 - November Week 4, 2012) were searched. Inclusion criteria were: included men with prostate cancer and/or their partners or caregivers who identify as Asian recruited in an Asian country; and assessed health-related quality of life, psychological and social adjustment relating to prostate cancer and published in English after 1st January 1999 and prior to 30th November, 2012. Study aims; design; quality; level of evidence, and key results were assessed. RESULTS: 43 articles met all inclusion criteria and were retained for initial review. Of these most focussed on health-related QOL with only five evidence Level IV studies from Japan and Taiwan including a specific psychological focus. Of these, one was a cross-sectional case control study; three were cross- sectional descriptive quantitative designs; one was a cross-sectional descriptive qualitative study. From the data available, a substantive sub group of men with prostate cancer (approximately one third) in these countries experience clinically high psychological distress and decision regret. CONCLUSIONS: Research on the psychological needs of men with the increasingly prevalent condition of prostate cancer in Asian countries is scant with only a small number of low level evidence descriptive studies identified. Future research to underpin the development and evaluation of effective and culturally relevant psychological and supportive care interventions for such men is urgently needed.


Subject(s)
Breast Neoplasms/mortality , Obesity/complications , Adult , Aged , Aged, 80 and over , Body Mass Index , Breast Neoplasms/etiology , Breast Neoplasms/pathology , Female , Follow-Up Studies , Humans , Lymphatic Metastasis , Male , Middle Aged , Neoplasm Staging , Obesity/physiopathology , Prognosis , Receptor, ErbB-2/metabolism , Receptors, Estrogen/metabolism , Receptors, Progesterone/metabolism , Retrospective Studies , Survival Rate , Young Adult
3.
World J Urol ; 21(3): 123-7, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12942275

ABSTRACT

The formation of an aesthetically desirable urinary diversion through a continent bladder stoma requires a long-term commitment by both patient and urologist to monitoring patient progress and addressing problems, both urological and otherwise, which arise over time. In this manuscript, issues relating to physical aspects of surgical management are discussed. These include the nature of and site of the stoma and its catheterizing track, the continence mechanism, provision of a low-pressure storage system of adequate capacity and management of the bladder neck/urethra when incompetent. It is imperative that careful patient selection is practised at the outset when such surgery is contemplated, otherwise a satisfactory outcome is unlikely to ensue irrespective of the procedural skills employed operatively.


Subject(s)
Cystostomy/methods , Humans , Urinary Catheterization , Urinary Reservoirs, Continent
4.
Urol Res ; 30(6): 347-55, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12599013

ABSTRACT

New vessel formation, a highly-regulated, active process commencing in the embryo and evident notably during the pubertal growth spurt, is essential for normal prostate development. Reactivation of this process in response to physiological stimuli, particularly hypoxia in mature tissues, occurs with new vessels forming principally from stromal components. Although angiogenesis is complex, putatively involving a multitude of angiogenic factors and inhibitors, there is powerful evidence of the importance of the VEGF system in the development of both the normal prostate and prostate cancer. Recent advances include an understanding of how castration acts through the VEGF system to inhibit angiogenesis. Stromal-endothelial and epithelial-endothelial interactions are just beginning to be investigated. A better understanding of how physiological angiogenesis is controlled should help to provide further insights into the mechanism of disregulated angiogenesis in tumours. Ultimately, new antiangiogenic agents are likely to find a role in the management of patients with prostate cancer.


Subject(s)
Neovascularization, Pathologic/physiopathology , Neovascularization, Physiologic/physiology , Prostate/blood supply , Prostate/growth & development , Prostatic Neoplasms/physiopathology , Animals , Humans , Male
5.
Int J Cancer ; 100(2): 228-37, 2002 Jul 10.
Article in English | MEDLINE | ID: mdl-12115574

ABSTRACT

The current approach to prostate cancer diagnosis has major limitations including the inability of prostate-specific antigen (PSA) assays to accurately differentiate between prostate cancer and benign prostate hyperplasia (BPH) and the imprecision of transrectal ultrasound (TRUS) biopsy sampling. We have employed cDNA microarray screening to compare gene expression patterns in BPH and tumour samples to identify expression markers that may be useful in discriminating between these conditions. Screening of 3 individual cDNA arrays identified 8 genes with expression 3-fold greater in 6 tumour tissues than in 1 nontumour sample and 1 BPH sample. Real-time PCR was used to confirm the overexpression of these 8 genes and 12 genes selected from the literature against a panel of 17 tumours and 11 BPH samples. Two genes, delta-catenin (delta-catenin; CTNND2) and prostate-specific membrane antigen (PSMA; FOLH1), were significantly overexpressed in prostate cancer compared to BPH. Prostate epithelial cells stained positively for delta-catenin and PSMA in our prostate cancer tissues, whereas the majority of our BPH tissues were negative for both markers. Thus we have identified delta-catenin (not previously associated with prostatic adenocarcinoma) and confirmed the potential of PSMA as potential candidates for the diagnosis and management of prostate cancer.


Subject(s)
Antigens, Neoplasm/genetics , Antigens, Surface , Biomarkers, Tumor , Carboxypeptidases/genetics , Cytoskeletal Proteins/genetics , Prostatic Hyperplasia/genetics , Adult , Aged , Aged, 80 and over , Armadillo Domain Proteins , Catenins , Cell Adhesion Molecules , DNA Primers/chemistry , Gene Expression Profiling , Gene Expression Regulation, Neoplastic , Glutamate Carboxypeptidase II , Humans , Immunoenzyme Techniques , In Situ Hybridization , Male , Middle Aged , Phosphoproteins , Polymerase Chain Reaction , Prostate-Specific Antigen/metabolism , Prostatic Hyperplasia/diagnosis , Prostatic Hyperplasia/surgery , Prostatic Neoplasms/diagnosis , Prostatic Neoplasms/genetics , Prostatic Neoplasms/surgery , Reverse Transcriptase Polymerase Chain Reaction , Transurethral Resection of Prostate , Delta Catenin
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