Paternity following treatment for testicular cancer

被引:180
作者
Brydoy, M
Fosså, SD
Klepp, O
Bremnes, RM
Wist, EA
Wentzel-Larsen, T
Dahl, O
机构
[1] Haukeland Hosp, Dept Oncol, N-5021 Bergen, Norway
[2] Haukeland Hosp, Clin Res Ctr, N-5021 Bergen, Norway
[3] Univ Bergen, Inst Med, Sect Oncol, Bergen, Norway
[4] St Olavs Univ Hosp, Trondheim, Norway
[5] Norwegian Univ Sci & Technol, N-7034 Trondheim, Norway
[6] Univ Hosp No Norway, Tromso, Norway
[7] Ullevaal Univ Hosp, Oslo, Norway
[8] Norwegian Radium Hosp, Oslo, Norway
[9] Univ Oslo, Fac Med, Oslo, Norway
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2005年 / 97卷 / 21期
关键词
D O I
10.1093/jnci/dji339
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Studies of fertility in men treated for testicular cancer have mainly addressed serum follicle-stimulating hormone levels and sperm parameters. We assessed post-treatment paternity among long-term survivors of testicular cancer. Methods: Men (n = 1814) who had been treated for unilateral testicular cancer in Norway during 1980 through 1994 were invited to participate in a national multi-center follow-up survey in 1998 through 2002. The participants were allocated to five groups according to the treatment received after orchiectomy, including treatment at relapse (surveillance, retroperitoneal lymph node dissection, radiotherapy, low-dose chemotherapy [i.e., <= 850 mg cisplatin], and high-dose chemotherapy [i.e., > 850 mg cisplatin]). Cox proportional hazards analysis was used to assess predictive factors for post-treatment paternity. Statistical tests were two-sided. Results: A total of 1433 men were assessable, of whom 827 were fathers at diagnosis. Posttreatment conception was attempted by 554 men, among whom the overall 15-year actuarial post-treatment paternity rate was 71% (95% confidence interval [CI] = 66% to 75%) without the use of cryopreserved semen. This rate ranged from 48% (95% CI = 30% to 69%) in the high-dose chemotherapy group to 92% (95% CI = 78% to 98%) in the surveillance group (P <.001). The median actuarial time from diagnosis to the birth of the first child after treatment was 6.6 years overall but varied according to treatment. Assisted reproductive technologies were used by 22% of the couples who attempted conception after treatment. Dry ejaculation, treatment group, pretreatment fatherhood, and marital status were statistically significant independent predictors for post-treatment fatherhood, with dry ejaculation as the most important negative factor. Conclusions: Although the overall paternity rate after treatment for testicular cancer was high, the ability to conceive and the time to conception reflected the intensity of treatment. These data may help inform patients about their future ability to father biological children.
引用
收藏
页码:1580 / 1588
页数:9
相关论文
共 56 条
[1]   PROGNOSTIC FACTORS IN UNSELECTED PATIENTS WITH NONSEMINOMATOUS METASTATIC TESTICULAR CANCER - A MULTICENTER EXPERIENCE [J].
AASS, N ;
KLEPP, O ;
CAVALLINSTAHL, E ;
DAHL, O ;
WICKLUND, H ;
UNSGAARD, B ;
BALDETORP, L ;
AHLSTROM, S ;
FOSSA, SD .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (05) :818-826
[2]  
Aass N, 1988, Prog Clin Biol Res, V269, P481
[3]   PREDICTION OF LONG-TERM GONADAL TOXICITY AFTER STANDARD TREATMENT FOR TESTICULAR CANCER [J].
AASS, N ;
FOSSA, SD ;
THEODORSEN, L ;
NORMAN, N .
EUROPEAN JOURNAL OF CANCER, 1991, 27 (09) :1087-1091
[4]   Sexuality and fertility in long-term survivors of testicular cancer [J].
Arai, Y ;
Kawakita, M ;
Okada, Y ;
Yoshida, O .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (04) :1444-1448
[5]  
BERTHELSEN JG, 1984, FERTIL STERIL, V41, P281
[6]   Fertility and sexual function following orchiectomy and 2 cycles of chemotherapy for stage I high risk nonseminomatous germ cell cancer [J].
Böhlen, D ;
Burkhard, FC ;
Mills, R ;
Sonntag, RW ;
Studer, UE .
JOURNAL OF UROLOGY, 2001, 165 (02) :441-444
[7]   NON-PATERNITY AND PRENATAL GENETIC SCREENING [J].
BROCK, DJH ;
SHRIMPTON, AE .
LANCET, 1991, 338 (8775) :1151-1151
[8]   ENDOCRINE AND EXOCRINE PROFILES OF MEN WITH TESTICULAR-TUMORS BEFORE ORCHIECTOMY [J].
CARROLL, PR ;
WHITMORE, WF ;
HERR, HW ;
MORSE, MJ ;
SOGANI, PC ;
BAJORUNAS, D ;
FAIR, WR ;
CHAGANTI, RSK .
JOURNAL OF UROLOGY, 1987, 137 (03) :420-423
[9]   Long-term efficacy of two cycles of BEP regimen in high-risk stage I nonseminomatous testicular germ cell tumors with embryonal carcinoma and/or vascular invasion [J].
Chevreau, C ;
Mazerolles, C ;
Soulié, M ;
Gaspard, MH ;
Mourey, L ;
Bujan, L ;
Plante, P ;
Rischmann, P ;
Bachaud, JM ;
Malavaud, B .
EUROPEAN UROLOGY, 2004, 46 (02) :209-215
[10]  
COMHAIRE FH, 1996, CLIN INVESTIGATION C, P133