Gonadal hormones in long-term survivors 10 years after treatment for unilateral testicular cancer

被引:128
作者
Nord, C [1 ]
Bjoro, T
Ellingsen, D
Mykletun, A
Dahl, O
Klepp, O
Bremnes, RM
Wist, E
Fosså, SD
机构
[1] Univ Hosp, Norwegian Radium Hosp, Dept Clin Res, N-0310 Oslo, Norway
[2] Univ Hosp, Norwegian Radium Hosp, Dept Cent Lab, N-0310 Oslo, Norway
[3] Natl Inst Occupat Hlth, Oslo, Norway
[4] Haukeland Univ Hosp, Dept Oncol, N-5021 Bergen, Norway
[5] Univ Bergen, Fac Psychol, Ctr Hlth Promot, Bergen, Norway
[6] Univ Trondheim Hosp, St Olavs Hosp, Dept Oncol, Trondheim, Norway
[7] Univ Hosp N Norway, Dept Oncol, Tromso, Norway
[8] Ullevaal Univ Hosp, Dept Oncol, Oslo, Norway
关键词
testicular cancer; LH; testosterone; ADAM; Leydig cell function;
D O I
10.1016/S0302-2838(03)00263-X
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective: To investigate whether unilaterally orchiectomised testicular cancer survivors (TCSs) are more likely to display reduced Leydig cell function than healthy males. Methods: A national multi-centre survey of 1235 TCSs was performed in 1998-2000 (mean age: 44 years) treated between 1980 and 1994 (mean follow-up: I I years). Serum hormone analyses were performed on 1183 TCSs, as 52 TCSs used androgen replacement (AR). TCSs were allocated to four treatment groups: Surgery only (251); Radiotherapy only (515); Chemotherapy 1, cisplatin less than or equal to850 mg (373); Chemotherapy 2, cisplatin >850 mg (96). The Controls were represented by 200 healthy blue-collar workers (mean age: 44 years). LH >12 IU/l and testosterone <8 nmol/l and the use of AR indicated hypogonadism. Results: Serum testosterone was similar in TCSs and Controls (16.9 vs. 17.1 nmol/1), but TCSs had higher age-adjusted LH levels than the Controls (5.2 vs. 3.5 IU/l). LH increased with treatment intensity, but was elevated even in TCSs treated with surgery only. The age-adjusted odds ratio of hypogonadism was 3.8 (95% Cl: 2.0-7.3) in TCSs, and increased with treatment intensity. Conclusion: TCSs are at risk to develop pre-mature reduced Leydig cell function and hypogonadism. They may therefore be predisposed for the syndrome of androgen deficiency of aging males (ADAM). (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:322 / 328
页数:7
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