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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorYamamoto, Noboru
dc.contributor.authorTolcher, Anthony
dc.contributor.authorHafez, Navid
dc.contributor.authorLugowska, Iwona
dc.contributor.authorRamlau, Rodryg
dc.contributor.authorMacarulla, Teresa
dc.date.accessioned2024-04-22T10:10:02Z
dc.date.available2024-04-22T10:10:02Z
dc.date.issued2024-03-29
dc.identifier.citationYamamoto N, Tolcher A, Hafez N, Lugowska I, Ramlau R, Macarulla T, et al. Efficacy and Safety of the MDM2-p53 Antagonist Brigimadlin (BI 907828) in Patients with Advanced Biliary Tract Cancer: A Case Series. Onco Targets Ther. 2024 Mar 29;17:267–80.
dc.identifier.issn1178-6930
dc.identifier.urihttps://hdl.handle.net/11351/11357
dc.descriptionBiliary tract cancer; Brigimadlin; Ezabenlimab
dc.description.abstractBackground: In patients with advanced biliary tract cancer (BTC), first-line chemotherapy plus immunotherapy has improved outcomes; however, second-line options that reflect the disease’s molecular heterogeneity are still needed. One emerging target is MDM2, amplified in ~5– 8% of BTC cases. Methods: This is a subset analysis of two ongoing Phase Ia/Ib trials assessing patients treated with brigimadlin (BI 907828; a highly potent, oral MDM2–p53 antagonist) ± ezabenlimab (PD-1 inhibitor) ± BI 754111 (anti-LAG-3; n = 1). Results: Results from 12 patients with BTC are shown (monotherapy: n = 6/combination: n = 6). Six patients achieved partial response (monotherapy: n = 2/combination: n = 4), four had stable disease; responses were durable. Brigimadlin had a manageable safety profile. Seven patients had dose reductions due to adverse events, but no treatment-related adverse events led to treatment discontinuation. Conclusion: Brigimadlin demonstrated anti-tumor activity in patients with advanced MDM2-amplified BTC, and warrants further investigation.
dc.language.isoeng
dc.publisherDove Medical Press
dc.relation.ispartofseriesOncoTargets and Therapy;17
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScientia
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectConductes biliars - Càncer - Tractament
dc.subjectQuimioteràpia combinada
dc.subjectProteïnes supressores de tumors
dc.subject.meshTreatment Outcome
dc.subject.meshBile Duct Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshTumor Suppressor Protein p53
dc.titleEfficacy and Safety of the MDM2–p53 Antagonist Brigimadlin (BI 907828) in Patients with Advanced Biliary Tract Cancer: A Case Series
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.2147/OTT.S440979
dc.subject.decsresultado del tratamiento
dc.subject.decsneoplasias de los conductos biliares
dc.subject.decs/farmacoterapia
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decsproteína supresora de tumor p53
dc.relation.publishversionhttps://doi.org/10.2147/OTT.S440979
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Yamamoto N] Department of Experimental Therapeutics, National Cancer Center Hospital, Tokyo, Japan. [Tolcher A] NEXT Oncology, San Antonio, TX, USA. [Hafez N] Yale Comprehensive Cancer Center, Yale School of Medicine, New Haven, CT, USA. The Angeles Clinic and Research Institute, A Cedars-Sinai Affiliate, Los Angeles, CA, USA. [Lugowska I] Early Phase Clinical Trials Unit, Maria Skłodowska Curie National Research Institute of Oncology, Warsaw, Poland. [Ramlau R] Institute of Oncology, Poznan University of Medical Sciences, Poznan, Poland. [Macarulla T] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.identifier.pmid38567193
dc.identifier.wos001194678500001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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