Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2026 Mar 1;36(2):147-154.
doi: 10.1097/MOU.0000000000001367. Epub 2026 Jan 5.

Sarcomatoid urothelial carcinoma: advances and challenges

Affiliations
Review

Sarcomatoid urothelial carcinoma: advances and challenges

Antonio Lopez-Beltran et al. Curr Opin Urol. .

Abstract

Purpose of review: This review provides a comprehensive and updated overview of current concepts, technical advances, and future directions regarding sarcomatoid urothelial carcinoma, an aggressive subtype of urothelial carcinoma that affects the urinary bladder and upper tract.

Recent findings: This review examines recent advances in pathology, molecular profiles, and molecular therapeutic targets in sarcomatoid urothelial carcinoma with emphasis on their clinical impact in practice. Recent data on chemotherapy and surgical approaches to these aggressive tumors are also discussed. Of relevance is the identification of sarcomatoid urothelial carcinoma as a basal molecular subtype, characterized by frequent expression of PD-1/PD-L1 and a potential response to immune checkpoint inhibitors. The status of other potential targets of novel therapies, such as Nectin-4, TROP2, FGFR3 , and HER2 , is also addressed.

Summary: The implications of new developments in clinical practice range from the corrected differential diagnosis of sarcomatoid urothelial carcinoma from its mimics to the potential value of neoadjuvant chemotherapy followed by radical cystectomy, and the use of immune checkpoint inhibitors in metastatic sarcomatoid urothelial cancer, which improve clinical management and offer survival benefits for these patients. The use of novel therapies targeting molecular pathways represents a significant advance, enabling more precise and individualized treatment strategies.

Keywords: Nectin-4; PD-L1; chemotherapy; cystectomy; sarcomatoid; targeted therapy.

PubMed Disclaimer

References

    1. Lopez-Beltran A, Pacelli A, Rothenberg HJ, et al. Carcinosarcoma and sarcomatoid carcinoma of the bladder: clinicopathological study of 41 cases. J Urol 1998; 159:1497–1503.
    1. Guo CC, Charles C, Majewski, et al. Dysregulation of EMT drives the progression to clinically aggressive sarcomatoid bladder cancer. Cell Rep 2019; 27:178.e41–1793.e4.
    1. Cheng L, Zhang S, Alexander R, et al. Sarcomatoid carcinoma of the urinary bladder: the final common pathway of urothelial carcinoma dedifferentiation. Am J Surg Pathol 2011; 35:e34–46.
    1. Wang X, MacLennan GT, Zhang S, et al. Sarcomatoid carcinoma of the upper urinary tract: clinical outcome and molecular characterization. Hum Pathol 2009; 40:211–217.
    1. Wright JL, Black PC, Brown GA, et al. Differences in survival among patients with sarcomatoid carcinoma, carcinosarcoma and urothelial carcinoma of the bladder. J Urol 2007; 178:2302–2307.

MeSH terms

Substances