Surgery versus surveillance in stage I non-seminoma testicular cancer

被引:0
|
作者
Sonneveld, DJA [1 ]
Koops, HS [1 ]
Sleijfer, DT [1 ]
Hoekstra, HJ [1 ]
机构
[1] Univ Groningen Hosp, Dept Surg Oncol, NL-9700 RB Groningen, Netherlands
来源
SEMINARS IN SURGICAL ONCOLOGY | 1999年 / 17卷 / 04期
关键词
testicular neoplasms; germ cell and embryonic neoplasms; neoplasm staging; adjuvant chemotherapy; lymph node excision; retroperitoneal space; radiotherapy; orchiectomy; X-ray computed tomography; neoplasm metastasis; lymphatic metastasis; cisplatin; combined antineoplastic agents; risk factors; survival rate; prognosis; postoperative complications; ejaculation; patient compliance; bleomycin/adverse effects; alpha-Fetoproteins; lactase dehydrogenase; chorionic gonadotropins;
D O I
10.1002/(SICI)1098-2388(199912)17:4<230::AID-SSU3>3.0.CO;2-U
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Today, the standard treatment for patients with clinical Stage I non-seminomatous testicular germ cell tumors (NSTGCT) following orchidectomy is either primary retroperitoneal lymph node dissection (RPLND) or close surveillance with cisplatin-based polychemotherapy in case of a relapse. Both treatment modalities provide excellent overall survival rates up to 100%. Consequently, selection of the most appropriate management option is not primarily guided by survival considerations. The choice between the available options, each having its merits and its drawbacks, should be made based on a number of factors including treatment-related morbidity, views and expertise of the physician, patient preferences, the expected degree of patient compliance, and prognostic factor analysis. To date, the role of adjuvant chemotherapy as an alternative management option for patients with clinical Stage I NSTGCT at high risk of occult metastases is limited. This systemic treatment modality would be a realistic alternative if the reliability of prognostic factors to identify high-risk Stage I patients could be improved. This review addresses relevant issues in the management of patients with clinical Stage I NSTGCT to provide information that will allow a rational selection of the most appropriate management option. Semin. Surg. Oncol. 17:230-239, 1999. (C) 1999 Wiley-Liss, Inc.
引用
收藏
页码:230 / 239
页数:10
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