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1.
Clin Endocrinol (Oxf) ; 88(3): 432-441, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29245176

RESUMO

OBJECTIVE: Cancer and its treatment in childhood and young adulthood can cause hypogonadism, leading to increased risk of long-term morbidity and mortality. The aim of this study was to evaluate the risk of presenting with biochemical signs of hypogonadism in testicular cancer survivors (TCS) and male childhood cancer survivors (CCS) in relation to the type of treatment given. DESIGN: Case-control study. PATIENTS: Ninety-two TCS, 125 CCS (mean age 40 and median age 34 years, respectively; mean follow-up time 9.2 and 24 years, respectively) and a corresponding number of age-matched controls. MEASUREMENTS: Fasting morning blood samples were analysed for total testosterone (TT), follicle-stimulating hormone (FSH) and luteinizing hormone (LH). The odds ratios (OR) for hypogonadism, defined as primary, secondary, compensated or ongoing androgen replacement, were calculated for TCS and CCS and for subgroups defined by diagnosis and treatment. RESULTS: Hypogonadism was found in 26% of CCS and 36% of TCS, respectively (OR: 2.1, P = .025 and OR = 2.3, P = .021). Among CCS, the OR was further increased in those given testicular irradiation (OR = 28, P = .004). Radiotherapy other than cranial or testicular irradiation plus chemotherapy, or cranial irradiation without chemotherapy, associated also with increased ORs (OR = 3.7, P = .013, and OR = 4.4, P = .038, respectively). Among TCS, those receiving >4 cycles of cisplatin-based chemotherapy had OR = 17, P = .015. CONCLUSIONS: Biochemical signs of testosterone deficiency are recognized as markers of decreased life expectancy. Thus, the risk of hypogonadism in TCS and CCS should be recognized and emphasizes the need of long-term follow-up for these men.


Assuntos
Sobreviventes de Câncer , Hipogonadismo/etiologia , Neoplasias Testiculares/complicações , Adolescente , Adulto , Estudos de Casos e Controles , Criança , Cisplatino/farmacologia , Humanos , Hipogonadismo/mortalidade , Hipogonadismo/radioterapia , Expectativa de Vida , Masculino , Fatores de Risco , Neoplasias Testiculares/terapia , Testosterona/deficiência , Adulto Jovem
2.
3.
Nat Rev Endocrinol ; 7(5): 267-78, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21423245

RESUMO

Prolactinomas, the most prevalent type of neuroendocrine disease, account for approximately 40% of all pituitary adenomas. The most important clinical problems associated with prolactinomas are hypogonadism, infertility and hyposexuality. In patients with macroprolactinomas, mass effects, including visual field defects, headaches and neurological disturbances, can also occur. The objectives of therapy are normalization of prolactin levels, to restore eugonadism, and reduction of tumor mass, both of which can be achieved in the majority of patients by treatment with dopamine agonists. Given their association with minimal morbidity, these drugs currently represent the mainstay of treatment for prolactinomas. Novel data indicate that these agents can be successfully withdrawn in a subset of patients after normalization of prolactin levels and tumor disappearance, which suggests the possibility that medical therapy may not be required throughout life. Nevertheless, multimodal therapy that involves surgery, radiotherapy or both may be necessary in some cases, such as patients who are resistant to the effects of dopamine agonists or for those with atypical prolactinomas. This Review reports on efficacy and safety of pharmacotherapy in patients with prolactinomas.


Assuntos
Prolactinoma/tratamento farmacológico , Agonistas de Dopamina/uso terapêutico , Humanos , Hipogonadismo/tratamento farmacológico , Hipogonadismo/fisiopatologia , Hipogonadismo/radioterapia , Hipogonadismo/cirurgia , Prolactina/metabolismo , Prolactinoma/fisiopatologia , Prolactinoma/radioterapia , Prolactinoma/cirurgia
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