2022
DOI: 10.1016/s1470-2045(21)00660-4
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Efficacy and safety of erdafitinib in patients with locally advanced or metastatic urothelial carcinoma: long-term follow-up of a phase 2 study

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Cited by 87 publications
(51 citation statements)
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“…In a phase 2 study by Loriot et al, erdafitinib was used to treat highgrade/metastatic BCa with FGFR alterations after chemotherapy or neoadjuvant therapy, and the ORR was nearly 40% (CRR of 3% and partial response rate of 37%) [161]. A recent long-term follow-up study by Radtke et al also confirmed the therapeutic activity of erdafitinib with an ORR of 40% (95% CI: 30-49%) and adverse events of stomatitis and hyponatremia of 14% and 11%, respectively [162].…”
Section: Oncolytic Virusesmentioning
confidence: 90%
“…In a phase 2 study by Loriot et al, erdafitinib was used to treat highgrade/metastatic BCa with FGFR alterations after chemotherapy or neoadjuvant therapy, and the ORR was nearly 40% (CRR of 3% and partial response rate of 37%) [161]. A recent long-term follow-up study by Radtke et al also confirmed the therapeutic activity of erdafitinib with an ORR of 40% (95% CI: 30-49%) and adverse events of stomatitis and hyponatremia of 14% and 11%, respectively [162].…”
Section: Oncolytic Virusesmentioning
confidence: 90%
“…Erdafitinib is an orally bioavailable selective and potent inhibitor of FGFR1–4 [ 17 ]. Erdafitinib was evaluated in an open-label, single-arm, phase II trial of 99 patients with locally advanced and unresectable or metastatic urothelial carcinoma with FGFR2 or 3 mutations or fusions who had progressed on prior platinum-based chemotherapy [ 51 , 52 ]. Notably, the dose of erdafitinib was guided by off-cancer on-target induction of hyperphosphatemia by inhibition of FGFR1.…”
Section: Fgfrsmentioning
confidence: 99%
“…The primary endpoint of objective response rate (ORR) was achieved in 40% of patients (3% complete, 37% partial). The median progression-free survival (PFS) was 5.5 months, and the median overall survival (OS) was 11.3 months after a median follow-up of 24 months [ 52 ]. The response rate was not affected by visceral metastasis.…”
Section: Fgfrsmentioning
confidence: 99%
“…It also reduces the activity of 1 alpha-hydroxylase and the production of calcitriol, thus decreasing the absorption of intestinal phosphate. FGF23 inhibitors are a new class of drugs approved for locally advanced or metastatic urothelial carcinoma and cholangiocarcinoma with genetic alterations [19][20][21][22][23]. FGFR inhibitors decrease the FGF23 enzyme activity and induce a decrease in phosphate renal excretion.…”
Section: Hyperphosphatemiamentioning
confidence: 99%