What is the damage? Testicular germ cell tumour survivors deficient in testosterone at risk of metabolic syndrome and a need for medical intervention

被引:5
|
作者
Poniatowska, Grazyna [1 ]
Michalski, Wojciech [1 ]
Kucharz, Jakub [1 ]
Jonska-Gmyrek, Joanna [1 ]
Wieszczy, Paulina [2 ,3 ]
Nietupski, Karol [1 ]
Demkow, Tomasz [1 ]
Dedecjus, Marek [4 ]
Sadowska, Malgorzata [1 ]
Kalinowski, Tomasz [1 ]
Grochulska-Nalazek, Beata [1 ]
Nowatorska, Ada [1 ]
Stelmasiak, Pawel [1 ]
Wiechno, Pawel J. [1 ]
机构
[1] Maria Sklodowska Curie Natl Res Inst Oncol, Dept Urooncol, 5 Roentgena St, PL-02781 Warsaw, Poland
[2] Med Ctr Postgrad Educ, Dept Gastroenterol Hepatol & Clin Oncol, Warsaw, Poland
[3] Maria Sklodowska Curie Natl Res Inst Oncol, Dept Canc Prevent, Warsaw, Poland
[4] Maria Sklodowska Curie Natl Res Inst Oncol, Dept Nucl Med & Endocrine Oncol, Warsaw, Poland
关键词
Hypogonadism; Metabolic syndrome; Testicular germ cell tumours; Testosterone; Deficiency; LONG-TERM SURVIVORS; CANCER-PATIENTS; HORMONE-LEVELS; HYPOGONADISM; DISTURBANCES; CHEMOTHERAPY; PREVALENCE; PLATINUM;
D O I
10.1007/s12032-020-01407-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Testicular germ cell tumours (TGCT) survivors are coping with late treatment sequelae. Testosterone deficiency may contribute to earlier onset of metabolic syndrome. The study aimed to assess connections between serum testosterone concentrations and metabolic disorders as well as body composition in TGCT survivors. 336 TGCT patients with over two years of complete post-treatment remission were divided into three groups: definite testosterone deficiency (< 8 nmol/L), 'grey zone' (8-12 nmol/L) and normal testosterone (> 12 nmol/L; control group) to assess differences in metabolism. Univariate and multivariate analyses were performed. The multivariate analysis assessed the risk of metabolic disorders and changes in body composition with regard to testosterone concentrations adjusted for age, smoking history, clinical stage, type of treatment and follow-up period. 14% of patients presented with definite testosterone deficiency; 46% were in the 'grey zone'. On multivariate analysis, low testosterone levels were related to hyperglycemia, hypercholesterolemia, hypertriglyceridemia, inflammatory processes, procoagulant state and obesity. The odds ratio (OR) for the onset of metabolic syndrome was 2.87 (95% CI 1.74-4.73,p < 0.001) for the 'grey zone' patients and 7.92 (95% CI 3.76-16.70,p < 0.001) for those with definite testosterone deficiency. Testosterone concentrations were independently associated with metabolic disorders in TGCT survivors. Testicular cancer survivors often have lower testosterone and metabolic disorders. Apart from recurrence, follow-up should focus on promoting a healthy lifestyle, preventing and managing late effects.
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页数:10
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共 14 条
  • [1] What is the damage? Testicular germ cell tumour survivors deficient in testosterone at risk of metabolic syndrome and a need for medical intervention
    Grazyna Poniatowska
    Wojciech Michalski
    Jakub Kucharz
    Joanna Jonska-Gmyrek
    Paulina Wieszczy
    Karol Nietupski
    Tomasz Demkow
    Marek Dedecjus
    Malgorzata Sadowska
    Tomasz Kalinowski
    Beata Grochulska-Nalazek
    Ada Nowatorska
    Pawel Stelmasiak
    Pawel J. Wiechno
    Medical Oncology, 2020, 37
  • [2] Re: What is the Damage? Testicular Germ Cell Tumour Survivors Deficient in Testosterone at Risk of Metabolic Syndrome and a Need for Medical Intervention
    Richie, Jerome P.
    JOURNAL OF UROLOGY, 2021, 205 (05): : 1517 - 1517
  • [3] Prevalence of the metabolic syndrome and cardiovascular disease risk in chemotherapy-treated testicular germ cell tumour survivors
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    N I Weijl
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    L van Wulften
    A Q M J van Steijn-van Tol
    F R Rosendaal
    S Osanto
    British Journal of Cancer, 2013, 109 : 60 - 67
  • [4] Prevalence of the metabolic syndrome and cardiovascular disease risk in chemotherapy-treated testicular germ cell tumour survivors
    Willemse, P. M.
    Burggraaf, J.
    Hamdy, N. A. T.
    Weijl, N. I.
    Vossen, C. Y.
    van Wulften, L.
    van Steijn-van Tol, A. Q. M. J.
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    BRITISH JOURNAL OF CANCER, 2013, 109 (01) : 60 - 67
  • [5] Comment on 'Prevalence of the metabolic syndrome and cardiovascular disease risk in chemotherapy-treated testicular germ cell tumour survivors'
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    BRITISH JOURNAL OF CANCER, 2013, 109 (09) : 2502 - 2503
  • [6] Erratum: Prevalence of the metabolic syndrome and cardiovascular disease risk in chemotherapy-treated testicular germ cell tumour survivors
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    L van Wulften
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  • [7] Comment on ‘Prevalence of the metabolic syndrome and cardiovascular disease risk in chemotherapy-treated testicular germ cell tumour survivors’
    M Singhera
    R Huddart
    British Journal of Cancer, 2013, 109 : 2502 - 2503
  • [8] Reply: 'Comment on Prevalence of the metabolic syndrome and cardiovascular disease risk in chemotherapy-treated testicular germ cell tumour survivors'
    Willemse, P. M.
    Burggraaf, J.
    Hamdy, N. A. T.
    Osanto, S.
    BRITISH JOURNAL OF CANCER, 2013, 109 (09) : 2503 - 2504
  • [9] Reply: ‘Comment on Prevalence of the metabolic syndrome and cardiovascular disease risk in chemotherapy-treated testicular germ cell tumour survivors’
    P M Willemse
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    N A T Hamdy
    S Osanto
    British Journal of Cancer, 2013, 109 : 2503 - 2504
  • [10] Re: Prevalence of the Metabolic Syndrome and Cardiovascular Disease Risk in Chemotherapy-Treated Testicular Germ Cell Tumour Survivors Editorial Comment
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    JOURNAL OF UROLOGY, 2013, 190 (05): : 1768 - 1768