Novel Therapeutic Approaches in Urothelial Carcinoma

A special issue of Medicina (ISSN 1648-9144). This special issue belongs to the section "Oncology".

Deadline for manuscript submissions: closed (30 March 2024) | Viewed by 2319

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Guest Editor
Division of Medical Oncology, Azienda Ospedaliero Universitaria Consorziale Policlinico di Bari, Bari, Italy
Interests: genitourinary neoplasms; cytotoxic chemotherapy; targeted therapies; immunotherapy; clinical trials
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Guest Editor
Department of Medical Oncology, Fondazione I.R.C.C.S. Istituto Nazionale dei Tumori, Milan, Italy
Interests: genitourinary neoplasms; cytotoxic chemotherapy; targeted therapies; immunotherapy; clinical trials

Special Issue Information

Dear Colleagues,

Urothelial carcinoma (UC) is the tenth most commonly diagnosed cancer worldwide. Historically, five-year survival rates for patients with locally advanced diseases are about 36%, but drop to about 5% for patients with distant metastases. In recent years, diagnostic and therapeutic advances have led to lower mortality rates for patients with urothelial carcinoma (UC). The standard of care for advanced urothelial carcinoma remains platinum-based combination chemotherapy, followed by maintenance or sequential immunotherapy. However, the therapeutic landscape has recently been expanded with the Food and Drug Administration’s (FDA’s) approval of erdafitinib for tumors with a mutation or fusion, which activates fibroblast growth factor receptor (FGFR) 2 or FGFR3. In addition, two drug-conjugated antibodies, enfortumab vedotin (EV) and sacituzumab govitecan (SG), are indicated after progression to platinum-based chemotherapy and programmed cell death inhibitor 1 (PD1) or programmed cell death ligand 1 (PD-L1). Furthermore, the adoption of stereotactic body radiation therapy (SBRT) in the management of oligometastatic urothelial carcinoma can improve disease control.

There are several clinical trials ongoing with novel agents and drug combinations to further expand the therapeutic horizon of urothelial carcinoma.

The increasing number of long-term responders to new systemic treatments requires early identification and appropriate management of known and emerging toxicities.

The next step is the large-scale analysis of somatic and germline genomics, aimed at the development of therapies directed at tumor-specific, druggable genetic targets. In addition, the identification of specific biomarkers is crucial for developing personalized therapeutic strategies for urothelial carcinoma patients.

We invite you and your colleagues to submit original research articles or reviews focusing on:

  • Genomic and molecular characterization of urothelial carcinoma;
  • Identification of prognostic and predictive biomarkers;
  • Future therapeutic perspectives;
  • Management of emerging therapies.

Dr. Mimma Rizzo
Dr. Patrizia Giannatempo
Guest Editors

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Keywords

  • urothelial carcinoma
  • immunotherapy
  • targeted therapies
  • antibody–drug conjugate
  • biomarker
  • radiotherapy

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Published Papers (1 paper)

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Review

20 pages, 904 KiB  
Review
Genomic Profiling and Molecular Characterisation of Metastatic Urothelial Carcinoma
by Gaetano Pezzicoli, Federica Ciciriello, Vittoria Musci, Silvia Minei, Antonello Biasi, Anna Ragno, Paola Cafforio and Mimma Rizzo
Medicina 2024, 60(4), 585; https://doi.org/10.3390/medicina60040585 - 31 Mar 2024
Cited by 1 | Viewed by 1924
Abstract
The clinical management of metastatic urothelial carcinoma (mUC) is undergoing a major paradigm shift; the integration of immune checkpoint inhibitors (ICIs) and antibody–drug conjugates (ADCs) into the mUC therapeutic strategy has succeeded in improving platinum-based chemotherapy outcomes. Given the expanding therapeutic armamentarium, it [...] Read more.
The clinical management of metastatic urothelial carcinoma (mUC) is undergoing a major paradigm shift; the integration of immune checkpoint inhibitors (ICIs) and antibody–drug conjugates (ADCs) into the mUC therapeutic strategy has succeeded in improving platinum-based chemotherapy outcomes. Given the expanding therapeutic armamentarium, it is crucial to identify efficacy-predictive biomarkers that can guide an individual patient’s therapeutic strategy. We reviewed the literature data on mUC genomic alterations of clinical interest, discussing their prognostic and predictive role. In particular, we explored the role of the fibroblast growth factor receptor (FGFR) family, epidermal growth factor receptor 2 (HER2), mechanistic target of rapamycin (mTOR) axis, DNA repair genes, and microsatellite instability. Currently, based on the available clinical data, FGFR inhibitors and HER2-directed ADCs are effective therapeutic options for later lines of biomarker-driven mUC. However, emerging genomic data highlight the opportunity for earlier use and/or combination with other drugs of both FGFR inhibitors and HER2-directed ADCs and also reveal additional potential drug targets that could change mUC management. Full article
(This article belongs to the Special Issue Novel Therapeutic Approaches in Urothelial Carcinoma)
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