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. Author manuscript; available in PMC: 2024 Jul 9.
Published in final edited form as: Clin Cancer Res. 2023 Nov 14;29(22):4586–4595. doi: 10.1158/1078-0432.CCR-23-1283

Table 3.

Cases of advanced/metastatic urothelial carcinoma treated with erdafitinib with subsequent acquisition of new notable cfDNA alterations prior to or at the time of disease progression.

Case ID Pre-treatment FGFR2/3 alterations Alterations acquired on erdafitinib related to TP53 and FGFR signaling Best response to erdafitinib by RECIST v1.1
P-0004257 FGFR3 Y373C TP53 K132M; TP53 R158L PR
P-0033799 FGFR3 S249C; FGFR3 S371C; FGFR3 R399C; FGFR3 R248C; TACC3-FGFR3 fusion FGFR3 R669Ga,b; FGFR3 V553Ma; FGFR3 N540Sa,b; FGFR3 H673Y; FGFR3 K649_K650delinsIEb,c; TP53 S241C; BRAF-CLIP2 fusion SD
P-0044554 FGFR3 S249C TP53 E287Q PD
P-0037307 FGFR3 S249C FGFR3 V553Ma; FGFR3 K650Mb,c; FGFR2 R255W; AKT1 E17K PR
P-0044518 FGFR3 S249C TP53 I195T PR
P-0042869 FGFR3 Y373C TP53 R248W; TP53 S241Y PR

Abbreviations: cfDNA, cell-free DNA; PD, progression of disease; PR, partial response; SD, stable disease

a

Putative FGFR3 gatekeeper mutation based on in silico analysis and/or preclinical data.

b

Likely pathogenic FGFR3 mutation based on OncoKB.

c

Hotspot FGFR3 mutation per OncoKB.