Ejaculation in testicular cancer patients after post-chemotherapy retroperitoneal lymph node dissection

被引:57
作者
Jacobsen, KD
Ous, S
Wæhre, H
Trasti, H
Stenwig, AE
Lien, HH
Aass, N
Fosså, SD
机构
[1] Norwegian Radium Hosp, Dept Med Oncol & Radiotherapy, N-0310 Oslo, Norway
[2] Norwegian Radium Hosp, Dept Surg Oncol, N-0310 Oslo, Norway
[3] Norwegian Radium Hosp, Dept Pathol, N-0310 Oslo, Norway
[4] Norwegian Radium Hosp, Dept Radiol, N-0310 Oslo, Norway
关键词
testicular cancer; nerve-sparing RPLND; fertility;
D O I
10.1038/sj.bjc.6690347
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this study was to evaluate fertility after different types of post-chemotherapy retroperitoneal lymph node dissection (RPLND). During 1980-1994, 192 patients with metastatic testicular cancer underwent post-chemotherapy RPLND with a gradual shift from modified bilateral template RPLND to nerve-sparing RPLND. Modified bilateral template RPLND was done in 92% of the patients operated during 1980-1984 as compared to 16% during 1989-1994. Pre- and post-treatment fertility was assessed by microscopic sperm analysis, determination of serum FSH and information on ejaculation and paternity. There was no significant difference of the survival rates between the three treatment periods. Antegrade ejaculation was preserved in 11% of the patients after modified bilateral template RPLND as compared to 89% after the nerve-sparing operation technique. The median ejaculatory Volume decreased post-operatively, serum FSH increased and sperm density remained unchanged. Fifty-six patients attempted fatherhood after their treatment, and 27 fathered at least one child after an observation-time of 55 months. nine of them by assisted fertilization. Patients with initially advanced testicular cancer but limited residual retroperitoneal masses after induction chemotherapy can safely undergo limited post-chemotherapy RPLND as a part of multimodality treatment. After nerve-sparing RPLND antegrade ejaculation is preserved in 89% of the patients though the ejaculatory volume decreases after RPLND. Post-treatment fatherhood can be achieved in at least 50% of the patients attempting paternity.
引用
收藏
页码:249 / 255
页数:7
相关论文
共 34 条
[1]  
Aass N, 1988, Prog Clin Biol Res, V269, P481
[2]   RENAL-FUNCTION RELATED TO DIFFERENT TREATMENT MODALITIES FOR MALIGNANT GERM-CELL TUMORS [J].
AASS, N ;
FOSSA, SD ;
AAS, M ;
LINDEGAARD, MW .
BRITISH JOURNAL OF CANCER, 1990, 62 (05) :842-846
[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]   RANDOMIZED TRIAL OF ETOPOSIDE AND CISPLATIN VERSUS ETOPOSIDE AND CARBOPLATIN IN PATIENTS WITH GOOD-RISK GERM-CELL TUMORS - A MULTIINSTITUTIONAL STUDY [J].
BAJORIN, DF ;
SAROSDY, MF ;
PFISTER, DG ;
MAZUMDAR, M ;
MOTZER, RJ ;
SCHER, HI ;
GELLER, NL ;
FAIR, WR ;
HERR, H ;
SOGANI, P ;
SHEINFELD, J ;
RUSSO, P ;
VLAMIS, V ;
CAREY, R ;
VOGELZANG, NJ ;
CRAWFORD, ED ;
BOSL, GJ .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (04) :598-606
[5]  
BERTHELSEN JG, 1984, FERTIL STERIL, V41, P281
[6]   LONG-TERM SEQUELAE OF TREATMENT FOR TESTICULAR GERM-CELL TUMORS [J].
BISSETT, D ;
KUNKELER, L ;
ZWANENBURG, L ;
PAUL, J ;
GRAY, C ;
SWAN, IRC ;
KERR, DJ ;
KAYE, SB .
BRITISH JOURNAL OF CANCER, 1990, 62 (04) :655-659
[7]   Testicular germ-cell cancer [J].
Bosl, GJ ;
Motzer, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (04) :242-253
[8]   EFFECT OF TREATMENT ON FERTILITY AND SEXUAL FUNCTION IN MALES WITH METASTATIC NONSEMINOMATOUS GERM-CELL TUMORS OF TESTIS [J].
BRENNER, J ;
VUGRIN, D ;
WHITMORE, WF .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1985, 8 (02) :178-182
[9]   NERVE-SPARING RETROPERITONEAL LYMPHADENECTOMY WITH PRESERVATION OF EJACULATION [J].
DONOHUE, JP ;
FOSTER, RS ;
ROWLAND, RG ;
BIHRLE, R ;
JONES, J ;
GEIER, G ;
JEWETT, MAS .
JOURNAL OF UROLOGY, 1990, 144 (02) :287-292
[10]   FERTILITY AFTER CHEMOTHERAPY FOR TESTICULAR CANCER [J].
DRASGA, RE ;
EINHORN, LH ;
WILLIAMS, SD ;
PATEL, DN ;
STEVENS, EE .
JOURNAL OF CLINICAL ONCOLOGY, 1983, 1 (03) :179-183