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   <dc:title>Targeting FGFR3 alterations with adjuvant infigratinib in invasive urothelial carcinoma: the phase III PROOF 302 trial</dc:title>
   <dc:creator>Pal, Sumanta</dc:creator>
   <dc:creator>Somford, Diederik M.</dc:creator>
   <dc:creator>Grivas, Petros</dc:creator>
   <dc:creator>Sridhar, Srikala S.</dc:creator>
   <dc:creator>Gupta, Shilpa</dc:creator>
   <dc:creator>Bellmunt Molins, Joaquim, 1959-</dc:creator>
   <dc:creator>Sonpavde, Guru</dc:creator>
   <dc:creator>Fleming, Mark T.</dc:creator>
   <dc:creator>Lerner, Seth Paul</dc:creator>
   <dc:creator>Loriot, Yohann</dc:creator>
   <dc:creator>Hoffman-Censits, Jean</dc:creator>
   <dc:creator>Valderrama, Begoña P.</dc:creator>
   <dc:creator>Andresen, Corina</dc:creator>
   <dc:creator>Schnabel, Marco J.</dc:creator>
   <dc:creator>Cole, Suzanne</dc:creator>
   <dc:creator>Daneshmand, Siamak</dc:creator>
   <dc:subject>FGFR inhibitor</dc:subject>
   <dc:subject>FGFR3</dc:subject>
   <dc:subject>PROOF 302</dc:subject>
   <dc:subject>Adjuvant cisplatin-based chemotherapy</dc:subject>
   <dc:subject>Adjuvant therapy</dc:subject>
   <dc:subject>Cisplatin-therapy refusal</dc:subject>
   <dc:subject>Fusions or rearrangements</dc:subject>
   <dc:subject>Infigratinib</dc:subject>
   <dc:subject>Muscle-invasive urothelial carcinoma</dc:subject>
   <dc:subject>Mutations</dc:subject>
   <dc:subject>Neoadjuvant cisplatin-based chemotherapy</dc:subject>
   <dc:subject>Phase III</dc:subject>
   <dc:subject>Upper tract urothelial carcinoma</dc:subject>
   <dc:subject>Urothelial bladder carcinoma</dc:subject>
   <dc:subject>Urothelial carcinoma</dc:subject>
   <dcterms:abstract>PROOF 302 is an ongoing randomized, double-blind, placebo-controlled, adjuvant phase III trial (NCT04197986) in approximately 218 patients from 120 centers worldwide. Eligibility criteria include post-surgical high-risk muscle-invasive upper tract urothelial cancer (85% of patients) or urothelial bladder cancer (15%), susceptible FGFR3 alterations (activating mutations, gene fusions or rearrangements), ≤120 days following radical surgery and ineligible for/or refusing cisplatin-based (neo)adjuvant chemotherapy. Patients receive either oral infigratinib 125 mg or placebo daily on days 1-21 of a 28-day cycle for up to 52 weeks or until recurrence, unacceptable toxicity or death. Primary end point: centrally determined disease-free survival (DFS); secondary end points: investigator-assessed DFS, metastasis-free survival, overall survival and safety/tolerability; exploratory end points: correlative biomarker analysis, quality-of-life and infigratinib pharmacokinetics.</dcterms:abstract>
   <dcterms:issued>2023-02-15T07:29:12Z</dcterms:issued>
   <dcterms:issued>2023-02-15T07:29:12Z</dcterms:issued>
   <dcterms:issued>2022</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:rights>This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Future Medicine</dc:publisher>
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