Benjamin David J, Kalebasty Arash Rezazadeh
Hoag Family Cancer Institute, Newport Beach, CA, USA.
Division of Hematology/Oncology, UC Irvine Medical Center, Orange, CA, USA.
Rare Tumors. 2023 Jul 14;15:20363613231189984. doi: 10.1177/20363613231189984. eCollection 2023.
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.
脐尿管癌是一种罕见的泌尿生殖系统恶性肿瘤,起源于脐尿管的胚胎残余组织。这种恶性肿瘤具有侵袭性,对于晚期疾病的恰当治疗尚无明确的共识。尽管传统上因其胚胎起源而被认为与膀胱癌有关,但多项新一代测序研究表明,这种泌尿生殖系统恶性肿瘤的基因组特征与结直肠癌最为相似。此外,这些研究还发现了包括表皮生长因子受体(EGFR)、 Kirsten大鼠肉瘤病毒癌基因(KRAS)和间质-上皮转化因子(MET)等在内的潜在可靶向治疗的突变。此外,近期数据表明免疫疗法可能使一些晚期脐尿管癌患者受益。尽管如此,仍需继续开展研究,以更好地了解如何治疗这种罕见的泌尿生殖系统癌症。