The cardiovascular risk of gonadotropin releasing hormone agonists in men with prostate cancer: An unresolved controversy
Critical Reviews in Oncology/Hematology, ISSN: 1040-8428, Vol: 86, Issue: 1, Page: 42-51
2013
- 55Citations
- 83Captures
Metric Options: Counts1 Year3 YearSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations55
- Citation Indexes52
- 52
- CrossRef26
- Policy Citations3
- Policy Citation3
- Captures83
- Readers83
- 83
Review Description
Gonadotropin-releasing hormone agonists (GnRH) play an important role in the treatment of prostate cancer, improving significantly overall survival. GnRH agonists belong to androgen deprivation therapy (ADT) together with surgical castration and, recently, GnRH antagonists. ADT has several side effects, such as sexual dysfunction and osteoporosis. Recently, changes in body composition, obesity, insulin resistance, hyperglycemia, dyslipidemia, and hypertension have emerged as complications of ADT, perhaps responsible for cardiovascular events, but discussion is still open. Since the majority of men with prostate cancer die of conditions other than their malignancy, recognition of these adverse effects is important. This review serves to focus attention on the pathogenetic mechanisms of ADT-related cardiovascular toxicity with also reference to the possible direct role of GnRH agonist on the cardiac receptors. Furthermore, this paper would generate recommendations for the management of patients treated with GnRH agonists balancing the potential benefits against the possible risks in prostate cancer men.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1040842812001916; http://dx.doi.org/10.1016/j.critrevonc.2012.09.008; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84875052064&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/23092636; https://linkinghub.elsevier.com/retrieve/pii/S1040842812001916
Elsevier BV
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