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睾丸旁横纹肌肉瘤的当前管理

Current management of paratesticular rhabdomyosarcoma.

作者信息

Dangle Pankaj P, Correa Andres, Tennyson Lauren, Gayed Bishoy, Reyes-Múgica Miguel, Ost Michael

机构信息

Division of Pediatric Urology, Children's Hospital of Pittsburgh, The University of Pittsburgh Medical Center, Pittsburgh, PA.

The University of Pittsburgh Medical Center, Pittsburgh, PA.

出版信息

Urol Oncol. 2016 Feb;34(2):84-92. doi: 10.1016/j.urolonc.2015.10.004. Epub 2015 Nov 11.

Abstract

OBJECTIVES

Paratesticular rhabdomyosarcoma accounts for 7-10% of genitourinary rhabdomyosarcoma tumors and is the 3rd most common after RMS of the prostate and bladder. Though most (60%-80%) patients with paratesticular rhabdomysarcoma present with localized disease, assessment of systemic disease is vital. The treatment of paratesticular rhabdomyosarcoma has evolved over several decades; the current standard of care is multimodal treatment including surgery, chemotherapy, and radiation. We give insight into the evolution of treatment, present the oncologic outcomes of seminal studies, and summarize the current recommendations for the management of these patients.

METHODS

A comprehensive search of the literature on the electronic databases PubMed was conducted for management of paratesticular rhabdomyosarcoma. Case reports were excluded, clinical trials from all the oncologic society were reviewed and relevant articles are included in the review.

RESULTS

The treatment regimen is based on following principles: (1) local control of the primary site with radical orchiectomy and (2) assessment of local control and distant sites. Further treatment is directed according to disease stage, histology, and age of the patient. The goal of treatment is to achieve cure or maximum tumor control while minimizing toxicity.

CONCLUSIONS

With the changing landscape in the management of paratesticular rhabomyosarcoma, significant improvement is evident in the oncologic outcomes. Further advance in genomic testing would lead us to tailor treatment based on individual risk factors and minimize long-term side effects.

摘要

目的

睾丸旁横纹肌肉瘤占泌尿生殖系统横纹肌肉瘤肿瘤的7%-10%,是继前列腺和膀胱横纹肌肉瘤之后第三常见的类型。尽管大多数(60%-80%)睾丸旁横纹肌肉瘤患者表现为局限性疾病,但评估全身疾病至关重要。睾丸旁横纹肌肉瘤的治疗在几十年间不断发展;目前的标准治疗是多模式治疗,包括手术、化疗和放疗。我们深入探讨治疗的演变,介绍重要研究的肿瘤学结果,并总结当前对这些患者管理的建议。

方法

在电子数据库PubMed上对睾丸旁横纹肌肉瘤的管理进行全面文献检索。排除病例报告,审查所有肿瘤学会的临床试验,并将相关文章纳入综述。

结果

治疗方案基于以下原则:(1)通过根治性睾丸切除术对原发部位进行局部控制,以及(2)评估局部控制和远处部位。根据疾病分期、组织学和患者年龄进行进一步治疗。治疗的目标是在将毒性降至最低的同时实现治愈或最大程度地控制肿瘤。

结论

随着睾丸旁横纹肌肉瘤管理格局的变化,肿瘤学结果有了显著改善。基因组检测的进一步进展将使我们能够根据个体风险因素定制治疗方案,并将长期副作用降至最低。

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