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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">The cornerstone of systemic treatment for prostate cancer is pharmacological or surgical androgen deprivation therapy &#40;ADT&#41;&#58;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a><ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">&#8226;</span><p id="par0010" class="elsevierStylePara elsevierViewall">For patients with metastatic prostate cancer&#44; ADT is the primary method of treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">&#8226;</span><p id="par0015" class="elsevierStylePara elsevierViewall">ADT is also used in combination with local treatment modalities to achieve better cancer control or as an effective salvage therapy in patients who do not respond to local therapy&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">&#8226;</span><p id="par0020" class="elsevierStylePara elsevierViewall">As many as 46&#37; of men with prostate cancer receive ADT at some point during their treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p></li></ul></p><p id="par0025" class="elsevierStylePara elsevierViewall">Pharmacological ADT refers to treatment with a gonadotropin-releasing hormone &#40;GnRH&#41; agonist or GnRH antagonist&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> Suppression of androgen signaling can also be accomplished with androgen receptor inhibitors or cytochrome P450 17A1 inhibitors&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Although ADT provides a means of effective cancer control&#44; studies have raised concerns regarding the adverse effects of ADT on metabolism and subsequent cardiovascular risk&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> The mechanisms through which ADT has been suspected to increase cardiovascular risk include increased fat mass&#44; increased low-density lipoprotein and total cholesterol&#44; increased triglycerides&#44; and increased insulin resistance&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Cardiovascular disease represents the most common comorbidity and cause of death among patients with prostate cancer&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> ADT had positive associations with cardiovascular events&#44; cardiovascular death&#44; and myocardial infarction&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">A number of studies have demonstrated that ADT is associated with fatal and nonfatal cardiovascular disease events that encompass ischemic heart disease&#44; myocardial infarction&#44; sudden cardiac death or ventricular arrhythmias&#44; cerebrovascular accidents&#44; peripheral artery disease&#44; and venous thromboembolism&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> Increased risk seems to occur regardless of whether the patient is administered short- or long-term ADT&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Epstein et al&#46; reported that death from ischemic heart disease is the most common noncancer death in patients with prostate cancer on ADT&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">The authors present a case that seems to be an example of acute myocardial infarction in an octogenarian patient on ADT with goserelin and bicalutamide&#46; Goserelin is a GnRH agonist and bicalutamide an androgen receptor inhibitor&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">They show other lesser-known manifestations of ADT that include QT interval prolongation and changes in repolarization presenting in a patient with chest pain&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Repolarization abnormalities and QT interval prolongation have been described with goserelin administration<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> and chest pain has been documented with bicalutamide&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">However&#44; the question remains&#44; despite the absence of coronary disease&#44; as to whether the chest pain and inversion of T waves would correspond to ischemia or not&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">The clinicians in this case decided to discontinue treatment with the drugs that caused the androgen deprivation and cardiac semiology regressed&#46; However&#44; we do not know what the subsequent attitude was&#46; Did they switch to a GnRH antagonist&#63;</p><p id="par0075" class="elsevierStylePara elsevierViewall">QT prolongation is a drug class effect due to androgen deprivation&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Prolongation of QT interval represents a delay in ventricular repolarization&#44; which may lead to ventricular tachyarrhythmias&#44; including torsade de pointes &#40;TdP&#41;&#46; TdP can degenerate into ventricular fibrillation&#44; leading to sudden death&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">Looking at this clinical case of cardiovascular effects of ADT makes us think that there is still a way to go in the search for knowledge&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of interest</span><p id="par0085" class="elsevierStylePara elsevierViewall">The author has no conflicts of interest to declare&#46;</p></span></span>"
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Knowing the true nature of the cardiovascular effects of androgen deprivation therapy in prostate cancer: We still have a way to go…
Complicações cardiovasculares da terapêutica de privação androgénica no cancro da próstata: ainda temos um caminho a percorrer para o seu correto diagnóstico…
Júlia Cristina Tostea,b
a Department of Cardiology, Hospital da Luz, Lisbon, Portugal
b NOVA Medical School, Lisbon, Portugal
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">The cornerstone of systemic treatment for prostate cancer is pharmacological or surgical androgen deprivation therapy &#40;ADT&#41;&#58;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a><ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">&#8226;</span><p id="par0010" class="elsevierStylePara elsevierViewall">For patients with metastatic prostate cancer&#44; ADT is the primary method of treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">&#8226;</span><p id="par0015" class="elsevierStylePara elsevierViewall">ADT is also used in combination with local treatment modalities to achieve better cancer control or as an effective salvage therapy in patients who do not respond to local therapy&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">&#8226;</span><p id="par0020" class="elsevierStylePara elsevierViewall">As many as 46&#37; of men with prostate cancer receive ADT at some point during their treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p></li></ul></p><p id="par0025" class="elsevierStylePara elsevierViewall">Pharmacological ADT refers to treatment with a gonadotropin-releasing hormone &#40;GnRH&#41; agonist or GnRH antagonist&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> Suppression of androgen signaling can also be accomplished with androgen receptor inhibitors or cytochrome P450 17A1 inhibitors&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Although ADT provides a means of effective cancer control&#44; studies have raised concerns regarding the adverse effects of ADT on metabolism and subsequent cardiovascular risk&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> The mechanisms through which ADT has been suspected to increase cardiovascular risk include increased fat mass&#44; increased low-density lipoprotein and total cholesterol&#44; increased triglycerides&#44; and increased insulin resistance&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Cardiovascular disease represents the most common comorbidity and cause of death among patients with prostate cancer&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> ADT had positive associations with cardiovascular events&#44; cardiovascular death&#44; and myocardial infarction&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">A number of studies have demonstrated that ADT is associated with fatal and nonfatal cardiovascular disease events that encompass ischemic heart disease&#44; myocardial infarction&#44; sudden cardiac death or ventricular arrhythmias&#44; cerebrovascular accidents&#44; peripheral artery disease&#44; and venous thromboembolism&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> Increased risk seems to occur regardless of whether the patient is administered short- or long-term ADT&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Epstein et al&#46; reported that death from ischemic heart disease is the most common noncancer death in patients with prostate cancer on ADT&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">The authors present a case that seems to be an example of acute myocardial infarction in an octogenarian patient on ADT with goserelin and bicalutamide&#46; Goserelin is a GnRH agonist and bicalutamide an androgen receptor inhibitor&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">They show other lesser-known manifestations of ADT that include QT interval prolongation and changes in repolarization presenting in a patient with chest pain&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Repolarization abnormalities and QT interval prolongation have been described with goserelin administration<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> and chest pain has been documented with bicalutamide&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">However&#44; the question remains&#44; despite the absence of coronary disease&#44; as to whether the chest pain and inversion of T waves would correspond to ischemia or not&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">The clinicians in this case decided to discontinue treatment with the drugs that caused the androgen deprivation and cardiac semiology regressed&#46; However&#44; we do not know what the subsequent attitude was&#46; Did they switch to a GnRH antagonist&#63;</p><p id="par0075" class="elsevierStylePara elsevierViewall">QT prolongation is a drug class effect due to androgen deprivation&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Prolongation of QT interval represents a delay in ventricular repolarization&#44; which may lead to ventricular tachyarrhythmias&#44; including torsade de pointes &#40;TdP&#41;&#46; TdP can degenerate into ventricular fibrillation&#44; leading to sudden death&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">Looking at this clinical case of cardiovascular effects of ADT makes us think that there is still a way to go in the search for knowledge&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of interest</span><p id="par0085" class="elsevierStylePara elsevierViewall">The author has no conflicts of interest to declare&#46;</p></span></span>"
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ISSN: 08702551
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Revista Portuguesa de Cardiologia
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