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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorGoyal, Lipika
dc.contributor.authorValle, Juan W
dc.contributor.authorMorizane, Chigusa
dc.contributor.authorMeric-Bernstam, Funda
dc.contributor.authorHollebecque, Antoine
dc.contributor.authorKarasic, Thomas
dc.contributor.authorTabernero, Josep
dc.date.accessioned2025-02-07T13:38:49Z
dc.date.available2025-02-07T13:38:49Z
dc.date.issued2024
dc.identifier.citationGoyal L, Meric-Bernstam F, Hollebecque A, Valle JW, Morizane C, Karasic TB. Plain language summary of the FOENIX-CCA2 study: futibatinib for people with advanced bile duct cancer. Futur Oncol. 2024;20(36):2811–22.
dc.identifier.issn1744-8301
dc.identifier.urihttps://hdl.handle.net/11351/12568
dc.descriptionCholangiocarcinoma; Futibatinib; Phase 2
dc.description.abstractWhat is this summary about?: This summary describes the results from a phase 2 study called FOENIXCCA2. The study evaluated treatment with futibatinib in people with a rare form of advanced bile duct cancer called intrahepatic cholangiocarcinoma (or iCCA), where the tumors have changes in the structure of a gene called FGFR2. These changes include FGFR2 gene fusions. Bile duct cancer often returns after surgery or cannot be treated by surgery because the tumor has spread, so it requires treatment with chemotherapy. People live for a median of 1 year after their first chemotherapy treatment and 6 months after their second treatment. This study included people whose cancer had grown/spread after one or more chemotherapy treatments. The aims of the study were to see if futibatinib could shrink the size of tumors and stop the cancer from growing/spreading and to see how long people lived when treated with futibatinib. Clinicians also looked at side effects from taking futibatinib and at how it affected people's quality of life. What were the results?: Futibatinib treatment shrank tumors in over 80% of people who received treatment. Tumors shrank by at least 30% in 42% of people. Futibatinib stopped tumors from growing/spreading for a median of 9.7 months. People who took the medicine lived for a median of 21.7 months, and 72% of people were still alive after 1 year. Side effects from taking futibatinib were like those reported for similar medicines, and clinicians considered the side effects to be manageable by adjusting the dose of futibatinib or treating the side effects. Most people reported that their quality of life stayed the same or improved during the first 9 months of taking futibatinib. What do the results mean?: The results support the use of futibatinib for treating people with advanced bile duct cancer. Based on the results of this study, futibatinib is now approved in the US, Europe, and Japan. Futibatinib is approved for treating adults with advanced bile duct cancer who have received previous treatment for their cancer, and whose tumors have a gene fusion or other change in the FGFR2 gene.Clinical Trial Registration: NCT02052778 (FOENIX-CCA2).
dc.language.isoeng
dc.publisherTaylor & Francis
dc.relation.ispartofseriesFuture Oncology;20(36)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectProteïnes quinases - Inhibidors - Ús terapèutic
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectConductes biliars - Càncer - Tractament
dc.subjectAdenocarcinoma - Tractament
dc.subjectAdenocarcinoma - Aspectes genètics
dc.subject.meshCholangiocarcinoma
dc.subject.mesh/drug therapy
dc.subject.meshBile Duct Neoplasms
dc.subject.meshProtein Kinase Inhibitors
dc.subject.mesh/therapeutic use
dc.subject.meshTreatment Outcome
dc.titlePlain language summary of the FOENIX-CCA2 study: futibatinib for people with advanced bile duct cancer
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1080/14796694.2024.2364504
dc.subject.decscolangiocarcinoma
dc.subject.decs/farmacoterapia
dc.subject.decsneoplasias de los conductos biliares
dc.subject.decsinhibidores de proteínas cinasas
dc.subject.decs/uso terapéutico
dc.subject.decsresultado del tratamiento
dc.relation.publishversionhttps://doi.org/10.1080/14796694.2024.2364504
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Goyal L] Department of Medicine, Stanford University School of Medicine, and the Stanford Cancer Center, Palo Alto, CA, USA. [Meric-Bernstam F] University of Texas MD Anderson Cancer Center, Houston, TX, USA. [Hollebecque A] Drug Development Department, Gustave Roussy, Villejuif, France. [Valle JW] Cholangiocarcinoma Foundation, Herriman, UT, USA. Division of Cancer Sciences, University of Manchester, Manchester, UK. [Morizane C] National Cancer Center Hospital, Tokyo, Japan. [Karasic TB] Hospital of the University of Pennsylvania, Philadelphia, PA, USA. [Tabernero J] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. University of Vic-Central University of Catalonia, Barcelona, Spain. Baselga Oncologic Institute, Hospital Quiron, Barcelona, Spain
dc.identifier.pmid38884254
dc.identifier.wos001249940600001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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