New Advances in Metastatic Urothelial Cancer: A Narrative Review on Recent Developments and Future Perspectives.
Humans
Immunoconjugates
/ therapeutic use
Neoplasm Metastasis
Immune Checkpoint Inhibitors
/ therapeutic use
Urologic Neoplasms
/ drug therapy
Antibodies, Monoclonal, Humanized
/ therapeutic use
Antineoplastic Agents
/ therapeutic use
Molecular Targeted Therapy
/ methods
Receptors, Fibroblast Growth Factor
/ antagonists & inhibitors
Antibodies, Monoclonal
/ therapeutic use
Urinary Bladder Neoplasms
/ drug therapy
Camptothecin
/ analogs & derivatives
FGFR
HER2
antibody–drug conjugate
enfortumab vedotin
erdafitinib
immune checkpoint inhibitors
sacituzumab govitecan
urothelial cancer
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
07 Sep 2024
07 Sep 2024
Historique:
received:
07
08
2024
revised:
03
09
2024
accepted:
05
09
2024
medline:
14
9
2024
pubmed:
14
9
2024
entrez:
14
9
2024
Statut:
epublish
Résumé
The standard of care for advanced or metastatic urothelial carcinoma (mUC) was historically identified with platinum-based chemotherapy. Thanks to the advances in biological and genetic knowledge and technologies, new therapeutic agents have emerged in this setting recently: the immune checkpoint inhibitors and the fibroblast growth factor receptor inhibitors as the target therapy for patients harboring alterations in the fibroblast growth factor receptor (FGFR) pathway. However, chasing a tumor's tendency to recur and progress, a new class of agents has more recently entered the scene, with promising results. Antibody-drug conjugates (ADCs) are in fact the latest addition, with enfortumab vedotin being the first to receive accelerated approval by the U.S. Food and Drug Administration in December 2019, followed by sacituzumab govitecan. Many other ADCs are still under investigation. ADCs undoubtedly represent the new frontier, with the potential of transforming the management of mUC treatment in the future. Therefore, we reviewed the landscape of mUC treatment options, giving an insight into the molecular basis and mechanisms, and evaluating new therapeutic strategies in the perspective of more and more personalized treatments.
Identifiants
pubmed: 39273642
pii: ijms25179696
doi: 10.3390/ijms25179696
pii:
doi:
Substances chimiques
Immunoconjugates
0
Immune Checkpoint Inhibitors
0
Antibodies, Monoclonal, Humanized
0
enfortumab vedotin
DLE8519RWM
Antineoplastic Agents
0
Receptors, Fibroblast Growth Factor
0
sacituzumab govitecan
M9BYU8XDQ6
Antibodies, Monoclonal
0
Camptothecin
XT3Z54Z28A
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM