Sexual dysfunction in nonseminoma testicular cancer patients is related to chemotherapy-induced angiopathy

被引:35
作者
vanBasten, JPA
Hoekstra, HJ
vanDriel, MF
Koops, HS
Droste, JHJ
JankerPool, G
vandeWiel, HBM
Sleijfer, DT
机构
[1] UNIV GRONINGEN HOSP,DEPT SURG ONCOL,NL-9700 RB GRONINGEN,NETHERLANDS
[2] UNIV GRONINGEN HOSP,DEPT UROL,NL-9700 RB GRONINGEN,NETHERLANDS
[3] UNIV GRONINGEN HOSP,DEPT EPIDEMIOL & STAT,NL-9700 RB GRONINGEN,NETHERLANDS
[4] UNIV GRONINGEN HOSP,DEPT PSYCHOL MED,NL-9700 RB GRONINGEN,NETHERLANDS
[5] UNIV GRONINGEN HOSP,DEPT MED ONCOL,NL-9700 RB GRONINGEN,NETHERLANDS
关键词
D O I
10.1200/JCO.1997.15.6.2442
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To establish the prevalence of sexual dysfunctions after different treatment modalities for non-seminomatous testicular germ cell tumor (NSTGCT) and to investigate whether treatment-induced angiopathy and neuropathy is related to sexual dysfunction. Patient and Methods: A questionnaire assessing sexual dysfunction was sent to 255 NSTGCT survivors, Polychemotherapy (PCT) regimens (cisplatin, vinblastine, and bleomycin [PVB], vinblastine substituted by etoposide [BEP], or cisplatin substituted by carboplatin [CEB], etoposide combined with cisplatin [EP], or with ifosfamide and cisplatin [VIP] were compared regarding treatment-induced angiopathy and neuropathy, Sexual dysfunctions were related to Raynaud's phenomenon and acral paresthesia, Results: Among the 215 responders, 56 (26%) had been treated by orchidectomy and surveillance, 42 (19.6%) by PCT, and 117 (54.4%) by PCT and resection of residual retroperitoneal turner mass (RRRTM), Overall, loss of libido was reported by 19.1%, decreased arousal by 11.2%, erectile dysfunction by 12.1%, decreased intensity of orgasm by 20%, and ejaculatory problems by 28%. Patients treated with PVB suffered more often from Raynaud's phenomenon compared with those treated with other regimens (40.4% v 29%; P < .05) and from paresthesia (31.6% v 14.7%; P < .05). Patients with Raynaud's phenomenon had more often erectile dysfunction (28.8%) compared with those without (8.4%) (P < .05). Conclusion: Compared with orchidectomy alone, PCT, with or without RRRTM, induced more often posttreatment sexual dysfunction. Compared with other chemotherapeutic regimens, signs of angiopathy and neuropathy were most prevalent ire those treated with PVB. Erectile dysfunction was related to the chemotherapy-induced Raynaud's phenomenon but not to acral paresthesia. (C) 1997 by American Society of Clinical Oncology.
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页码:2442 / 2448
页数:7
相关论文
共 58 条
[1]   PRETREATMENT AND POSTTREATMENT SEXUAL LIFE IN TESTICULAR CANCER-PATIENTS - A DESCRIPTIVE INVESTIGATION [J].
AASS, N ;
GRUNFELD, B ;
KAALHUS, O ;
FOSSA, SD .
BRITISH JOURNAL OF CANCER, 1993, 67 (05) :1113-1117
[2]  
ALEXANDER GM, 1991, HORM BEHAV, V26, P367
[3]   Psychosocial aspects in long-term survivors of testicular cancer [J].
Arai, Y ;
Kawakita, M ;
Hida, S ;
Terachi, T ;
Okada, Y ;
Yoshida, O .
JOURNAL OF UROLOGY, 1996, 155 (02) :574-578
[4]   ERECTILE DYSFUNCTION DUE TO ATHEROSCLEROTIC VASCULAR-DISEASE - THE DEVELOPMENT OF AN ANIMAL-MODEL [J].
AZADZOI, KM ;
GOLDSTEIN, I .
JOURNAL OF UROLOGY, 1992, 147 (06) :1675-1681
[5]   Drug therapy - Androgens in men - Uses and abuses [J].
Bagatell, CJ ;
Bremner, WJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (11) :707-714
[6]   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
[7]  
BANCROFT J, 1989, HUMAN SEXUALITY ITS, P12
[8]   Endocrinological late effects after chemotherapy for testicular cancer [J].
Berger, CC ;
Bokemeyer, C ;
Schuppert, F ;
Schmoll, HJ .
BRITISH JOURNAL OF CANCER, 1996, 73 (09) :1108-1114
[9]   Secondary Raynaud's phenomenon and other late vascular complications following chemotherapy for testicular cancer [J].
Berger, CC ;
Bokemeyer, C ;
Schneider, M ;
Kuczyk, MA ;
Schmoll, HJ .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (13-14) :2229-2238
[10]   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