Literature DB >> 33475078

Erdafitinib as a Novel and Advanced Treatment Strategy of Metastatic Urothelial Carcinoma.

Parveen Bansal1, Deepak K Dwivedi2, Deepa Hatwal2, Priyanka Sharma1, Vikas Gupta1, Suresh Goyal3, Mukesh Maithani2.   

Abstract

Urothelial carcinoma has become the ninth most common malignancy in the world. Since the 1980s, diverse studies and treatment methods came out with their possible effects along with certain limitations. Initially, platinum chemotherapy was considered as first-line treatment of the disease. Although it was proved to be effective initially, the most number of cases reported the reoccurrence of the disease. Furthermore, aberrant ligand- dependent and constitutive ligand-independent fibroblast growth factor receptor (FGFR) signaling has been reported in a large number of solid tumors, including urothelial carcinoma that became the basis for FGFR inhibition for the treatment of the disease. Erdafitinib is a pan-FGFR inhibitor that was recently approved in the USA for the treatment of locally advanced or metastatic FGFR3 or FGFR2 urothelial carcinoma. The drug is also being investigated as a treatment for other cancers, including cholangiocarcinoma, liver cancer, non-small cell lung cancer, prostate cancer, lymphoma cancer and oesophageal cancer. This article summarizes the various treatments that evolved for bladder cancer till now, a brief description of the biology of FGFR inhibition, clinical pharmacology, and various clinical trials of erdafitinib. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

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Keywords:  Urinary bladder neoplasm; chemotherapy adjuvant; clinicalzzm321990trials; erdafitinib.; fibroblast growth factor; pharmacodynamics; pharmacokinetics

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Year:  2021        PMID: 33475078     DOI: 10.2174/1871520621666210121093852

Source DB:  PubMed          Journal:  Anticancer Agents Med Chem        ISSN: 1871-5206            Impact factor:   2.505


  2 in total

1.  Erdafitinib Inhibits Tumorigenesis of Human Lung Adenocarcinoma A549 by Inducing S-Phase Cell-Cycle Arrest as a CDK2 Inhibitor.

Authors:  Xinmin Meng; Xue Zhu; Jiali Ji; Hongqin Zhong; Xiyue Li; Hongqing Zhao; Guijuan Xie; Ke Wang; Hong Shu; Xun Wang
Journal:  Molecules       Date:  2022-10-09       Impact factor: 4.927

2.  Insights of fibroblast growth factor receptor 3 aberrations in pan-cancer and their roles in potential clinical treatment.

Authors:  Juanni Li; Kuan Hu; Jinzhou Huang; Lei Zhou; Yuanliang Yan; Zhijie Xu
Journal:  Aging (Albany NY)       Date:  2021-06-23       Impact factor: 5.682

  2 in total

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