尿管癌的治疗方法:使用免疫治疗和靶向治疗。

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2023-01-01 DOI:10.1177/20363613231189984
David J Benjamin, Arash Rezazadeh Kalebasty
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引用次数: 1

摘要

尿管癌是一种罕见的泌尿生殖系统恶性肿瘤,起源于胚胎残余的尿管。恶性肿瘤被认为是侵袭性的,对于晚期疾病的适当治疗没有明确的共识。虽然传统上认为由于其胚胎起源与膀胱癌有关,但几项下一代测序研究揭示了这种泌尿生殖系统恶性肿瘤的基因组图谱与结直肠癌最相似。此外,这些研究已经确定了潜在的可操作突变,包括EGFR, KRAS和MET。此外,最近的数据表明免疫疗法可能使一些晚期尿管癌患者受益。尽管如此,为了更好地了解如何治疗这种罕见的泌尿生殖系统癌,需要继续进行研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Treatment approaches for urachal cancer: Use of immunotherapy and targeted therapies.

Urachal cancer is a rare genitourinary malignancy that arises from the embryologic remnant of the urachus. The malignancy is considered to be aggressive, with no clear consensus on appropriate management for advanced disease. Although traditionally considered to be related to bladder cancer given its embryologic origin, several next generation sequencing studies have revealed the genomic profile of this genitourinary malignancy most closely resembles colorectal cancer. Moreover, these studies have identified potentially actionable mutations including EGFR, KRAS and MET. In addition, recent data suggests that immunotherapy may benefit some patients with advanced urachal cancer. Nonetheless, continued research is warranted to better understand how to treat this rare genitourinary cancer.

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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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