The evolving treatment landscape of advanced urothelial carcinoma
Alexander Y Andreev-Drakhlin1, Goar Egoryan2, Amishi Y Shah1,3
1Division of Cancer Medicine, MD Anderson Cancer Center, Houston, Texas.
Purpose Of Review:
Bladder cancer is the 10th most common cancer in the world and the 6th most common cancer among men. In the past few years, several new agents have been approved for the treatment of urothelial tumors. In this paper, we review the evolving treatment landscape of advanced urothelial carcinoma (UC).
Recent Findings:
Since 2016, the Food and Drug Administration (FDA) has approved five immunotherapies targeting programmed cell death 1/programmed cell death 1 legend, an antinectin-4 antibody drug conjugate (ADC), and a fibroblast growth factor receptor (FGFR) inhibitor for the treatment of patients with advanced UC. Moreover, there are multiple targeted agents, immune checkpoint inhibitors (ICI), ADCs, and their combinations currently being tested in clinical studies with the goal of obtaining FDA approval.
Summary:
Precision oncology efforts continue to advance our understanding of the UC biology and transform the existing treatment paradigms. An enlarging arsenal of treatment options promises further personalization of UC therapy.
Insights
Recent advancements offer new treatments for advanced urothelial carcinoma (UC), a common cancer. New immunotherapies, antibody drug conjugates, and targeted agents are transforming bladder cancer care.
Area of Science:
- Oncology
- Urology
- Cancer Research
Background:
- Bladder cancer is a significant global health concern, ranking as the 10th most common cancer worldwide and 6th among men.
- Urothelial carcinoma (UC) represents the majority of bladder cancer cases.
- The treatment landscape for advanced UC has been historically limited.
Purpose of the Study:
- To review the evolving treatment landscape for advanced urothelial carcinoma (UC).
- To highlight recent therapeutic approvals and ongoing clinical investigations in UC treatment.
Main Methods:
- Literature review of recent clinical studies and FDA approvals for advanced UC.
- Analysis of emerging therapeutic classes including immunotherapies, antibody-drug conjugates, and targeted agents.
Main Results:
- Since 2016, the FDA has approved five immunotherapies (targeting PD-1/PD-L1), an anti-Nectin-4 antibody-drug conjugate (ADC), and a fibroblast growth factor receptor (FGFR) inhibitor for advanced UC.
- Multiple targeted agents, immune checkpoint inhibitors (ICIs), ADCs, and combination therapies are under active clinical investigation.
- These advancements represent a significant expansion of treatment options for patients with advanced UC.
Conclusions:
- Precision oncology is rapidly advancing the understanding and treatment of UC.
- An expanding array of therapeutic options enables greater personalization of UC therapy.
- The future of advanced UC treatment involves targeted therapies and immunomodulatory agents.
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