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睾丸临床I期非精原细胞瘤生殖细胞肿瘤的当前管理更新

Current update of management of clinical stage I non seminomatous germ cell tumors of testis.

作者信息

Yuvaraja T B

机构信息

Consultant Uro-Oncologist, Centre for Cancer, kokilaben Dhirubhai Ambani Hospital, Four Bungalows, Andheri West, Mumbai, 400053 India.

出版信息

Indian J Surg Oncol. 2012 Jun;3(2):101-6. doi: 10.1007/s13193-012-0124-8. Epub 2012 Mar 20.

Abstract

The management of patients with testicular germ cell tumors (GCT) has evolved significantly over the past 30 years with cure rates approaching nearly 100% for low-stage disease and more than 80% for advanced disease. Controversy surrounds about ideal management of clinical stage I non seminomatous germ cell tumors (CS I NSGCT) of the testis due to multiple treatment options available with more or less equal efficacy. Nerve-sparing retroperitoneal lymph node dissection (RPLND), adjuvant chemotherapy with two cycles of bleomycin, etoposide, and cisplatin , or surveillance have all achieved long-term survival in nearly 100% of patients with clinical stage I NSGCT. Retroperitoneal lymph node dissection is still favoured as the therapy of choice for clinical stage I non-seminomatous germ cell tumors in many centres, but as risk factors for the primary tumor have become better understood, surveillance and risk-adapted therapy, including surveillance for low-risk patients and adjuvant chemotherapy for the high-risk group, is now being considered a therapeutic option. The objective of this study is to review current developments in the management of CS I NSGCT testis with emphasis on risk stratification and treatment recommendations.

摘要

在过去30年中,睾丸生殖细胞肿瘤(GCT)患者的管理有了显著进展,低分期疾病的治愈率接近100%,晚期疾病的治愈率超过80%。由于有多种疗效大致相当的治疗选择,睾丸临床I期非精原细胞性生殖细胞肿瘤(CS I NSGCT)的理想管理存在争议。保留神经的腹膜后淋巴结清扫术(RPLND)、两周期博来霉素、依托泊苷和顺铂辅助化疗或监测,在几乎100%的临床I期NSGCT患者中均实现了长期生存。在许多中心,腹膜后淋巴结清扫术仍是临床I期非精原细胞性生殖细胞肿瘤的首选治疗方法,但随着对原发性肿瘤危险因素的认识更加深入,监测和风险适应性治疗,包括对低风险患者的监测和对高风险组的辅助化疗,现在被视为一种治疗选择。本研究的目的是回顾CS I NSGCT睾丸管理的当前进展,重点是风险分层和治疗建议。

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本文引用的文献

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BJU Int. 2009 Nov;104(9 Pt B):1351-6. doi: 10.1111/j.1464-410X.2009.08858.x.
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