SP-0053 LDR prostate brachytherapy is safe and effective for all localized prostate cancer risk groups

2021 ◽  
Vol 158 ◽  
pp. S41
Author(s):  
B. Davis
2002 ◽  
Vol 20 (19) ◽  
pp. 4129-4130 ◽  
Author(s):  
James R. Gray ◽  
Chaundre Cross ◽  
Anthony D’Amico

2020 ◽  
Vol 14 (10) ◽  
Author(s):  
Rehana Rasul ◽  
Anne Golden ◽  
Michael A. Feuerstein

Introduction: Informed decision-making in localized prostate cancer must consider the natural history of the disease, risks of treatment, and the competing risks from other causes. Other-cause mortality has often been associated with comorbidity or treatment-related side effects. We aimed to examine the association between prostate cancer aggressiveness and other cause mortality. Methods: Using the Surveillance, Epidemiology, and End Results’ (SEER)18 registries, patients diagnosed with localized prostate cancer between 2004 and 2015 were identified. Patients were categorized into low-, intermediate- and high-risk groups. Vital status, death due to prostate cancer and death due to other causes were based on death certificate information. Survival analyses were performed to assess the association between prostate cancer risk group and mortality while adjusting for demographic variables, year of diagnosis, and initial therapy. Results: A total of 464 653 patients were identified with a median followup of 5.4 years. Cardiovascular disease was the most common cause of mortality during the study period. Compared to low-risk patients, intermediate- and high-risk patients had a higher risk of mortality from other cancers, from cardiovascular disease, and from other causes of death regardless of initial treatment. Men who underwent surgery as initial therapy had lower cumulative mortality rates compared to those with radiation as their initial therapy. Conclusions: Intermediate- and high-risk prostate cancers are associated with higher risk of other-cause mortality. This appears to be independent of treatment type and may not be solely explained by comorbidity status. Further studies controlling for comorbidity and treatment burden should be explored.


2010 ◽  
Vol 28 (7) ◽  
pp. 1117-1123 ◽  
Author(s):  
Matthew R. Cooperberg ◽  
Jeanette M. Broering ◽  
Peter R. Carroll

Purpose In the absence of high-level evidence or clinical guidelines supporting any given active treatment approach over another for localized prostate cancer, clinician and patient preferences may lead to substantial variation in treatment use. Methods Data were analyzed from 36 clinical sites that contributed data to the Cancer of the Prostate Strategic Urologic Research Endeavor (CaPSURE) registry. Distribution of primary treatment use was measured over time. Prostate cancer risk was assessed using the D'Amico risk groups and the Cancer of the Prostate Risk Assessment (CAPRA) score. Descriptive analyses were performed, and a hierarchical model was constructed that controlled for year of diagnosis, cancer risk variables, and other patient factors to estimate the proportion of variation in primary treatment selection explicable by practice site. Results Among 11,892 men analyzed, 6.8% elected surveillance, 49.9% prostatectomy, 11.6% external-beam radiation, 13.3% brachytherapy, 4.0% cryoablation, and 14.4% androgen deprivation monotherapy. Prostate cancer risk drives treatment selection, but the data suggest both overtreatment of low-risk disease and undertreatment of high-risk disease. The former trend appears to be improving over time, while the latter is worsening. Treatment varies with age, comorbidity, and socioeconomic status. However, treatment patterns vary markedly across clinical sites, and this variation is not explained by case-mix variability or known patient factors. Practice site explains a proportion of this variation ranging from 13% for androgen deprivation monotherapy to 74% for cryoablation. Conclusion Substantial variation exists in management of localized prostate cancer that is not explained by measurable factors. A critical need exists for high-quality comparative effectiveness research in localized prostate cancer to help guide treatment decision making.


2018 ◽  
Vol 199 (4S) ◽  
Author(s):  
Sean A. Fletcher ◽  
Nicolas von Landenberg ◽  
Alexander P. Cole ◽  
Sebastian Berg ◽  
Philipp Gild ◽  
...  

2018 ◽  
Vol 17 (2) ◽  
pp. e1515-e1517
Author(s):  
S. Fletcher ◽  
A. Cole ◽  
N. Von Landenberg ◽  
S. Berg ◽  
P. Gild ◽  
...  

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