Infigratinib in patients with advanced cholangiocarcinoma with FGFR2 gene fusions/translocations: the PROOF 301 trial

Cholangiocarcinoma is an aggressive malignancy with poor overall survival. Approximately 15% of intrahepatic cholangiocarcinomas contain FGFR alterations. Infigratinib is an oral FGFR 1–3 kinase inhibitor. Favorable results from a Phase II trial of infigratinib in advanced/metastatic FGFR-altered ch...

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Veröffentlicht in:Future oncology (London, England) England), 2020-10, Vol.16 (30), p.2375-2384
Hauptverfasser: Makawita, Shalini, K Abou-Alfa, Ghassan, Roychowdhury, Sameek, Sadeghi, Saeed, Borbath, Ivan, Goyal, Lipika, Cohn, Allen, Lamarca, Angela, Oh, Do-Youn, Macarulla, Teresa, T Shroff, Rachna, Howland, Michael, Li, Ai, Cho, Terry, Pande, Amit, Javle, Milind
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Sprache:eng
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Zusammenfassung:Cholangiocarcinoma is an aggressive malignancy with poor overall survival. Approximately 15% of intrahepatic cholangiocarcinomas contain FGFR alterations. Infigratinib is an oral FGFR 1–3 kinase inhibitor. Favorable results from a Phase II trial of infigratinib in advanced/metastatic FGFR-altered cholangiocarcinomas has led to its further investigation in the front-line setting. In this article we describe the design, objectives and rationale for PROOF 301, a Phase III multicenter, open label, randomized trial of infigratinib in comparison to standard of care gemcitabine and cisplatin in advanced/metastatic cholangiocarcinoma with FGFR2 translocations. The results of this study have the potential to define a new role for a chemotherapy-free, targeted therapy option in the front-line setting for these patients. Clinical Trial Registration: NCT03773302 (ClincalTrials.gov)
ISSN:1479-6694
1744-8301
DOI:10.2217/fon-2020-0299