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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorHummel, Horst-Dieter
dc.contributor.authorChampiat, Stephane
dc.contributor.authorOlmedo García, María Eugenia
dc.contributor.authorHe, Kai
dc.contributor.authorDowlati, Afshin
dc.contributor.authorBoyer, Michael
dc.contributor.authorFELIP, ENRIQUETA
dc.date.accessioned2025-02-18T11:10:40Z
dc.date.available2025-02-18T11:10:40Z
dc.date.issued2024-10-10
dc.identifier.citationDowlati A, Hummel HD, Champiat S, Olmedo ME, Boyer M, He K, et al. Sustained Clinical Benefit and Intracranial Activity of Tarlatamab in Previously Treated Small Cell Lung Cancer: DeLLphi-300 Trial Update. J Clin Oncol. 2024 Oct 10;42(29):3392–9.
dc.identifier.issn1527-7755
dc.identifier.urihttps://hdl.handle.net/11351/12617
dc.descriptionImmunotherapy; Small cell lung cancer
dc.description.abstractClinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported. Tarlatamab, a bispecific T-cell engager immunotherapy targeting delta-like ligand 3, has shown durable anticancer activity and manageable safety in previously treated small cell lung cancer (SCLC) in DeLLphi-300 phase I and DeLLphi-301 phase II trials. Here, we report extended follow-up of DeLLphi-300 (median follow-up, 12.1 months [range, 0.2-34.3]) in fully enrolled cohorts treated with tarlatamab ≥10 mg dose administered once every two weeks, once every three weeks, or once on day 1 and once on day 8 of a 21-day cycle (N = 152). Overall, the objective response rate (ORR) was 25.0%; the median duration of response (mDOR) was 11.2 months (95% CI, 6.6 to 22.3), and the median overall survival (mOS) was 17.5 months (95% CI, 11.4 to not estimable [NE]). Among 17 patients receiving 10 mg tarlatamab once every two weeks, the ORR was 35.3%, the mDOR was 14.9 months (95% CI, 3.0 to NE), the mOS was 20.3 months (95% CI, 5.1 to NE), and 29.4% had sustained disease control with time on treatment ≥52 weeks. No new safety signals were identified. In modified Response Assessment in Neuro-Oncology Brain Metastases analyses, CNS tumor shrinkage of ≥30% was observed in 62.5% of patients (10 of 16) who had a baseline CNS lesion of ≥10 mm, including in a subset of patients with tumor shrinkage long after previous brain radiotherapy. In DeLLphi-300 extended follow-up, tarlatamab demonstrated unprecedented survival and potential findings of intracranial activity in previously treated SCLC.
dc.language.isoeng
dc.publisherAmerican Society of Clinical Oncology
dc.relation.ispartofseriesJournal of Clinical Oncology;42(29)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectPulmons - Càncer - Immunoteràpia
dc.subjectCervell - Càncer - Immunoteràpia
dc.subjectMedicaments antineoplàstics - Ús terapèutic
dc.subject.meshSmall Cell Lung Carcinoma
dc.subject.mesh/drug therapy
dc.subject.meshBrain Neoplasms
dc.subject.meshAntineoplastic Agents, Immunological
dc.subject.mesh/therapeutic use
dc.titleSustained Clinical Benefit and Intracranial Activity of Tarlatamab in Previously Treated Small Cell Lung Cancer: DeLLphi-300 Trial Update
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1200/JCO.24.00553
dc.subject.decscarcinoma pulmonar de células pequeñas
dc.subject.decs/farmacoterapia
dc.subject.decsneoplasias cerebrales
dc.subject.decsinmunoterapia antineoplásica
dc.subject.decs/uso terapéutico
dc.relation.publishversionhttps://doi.org/10.1200/JCO.24.00553
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Dowlati A] University Hospitals Seidman Cancer Center and Case Western Reserve University, Cleveland, OH. [Hummel HD] Translational Oncology/Early Clinical Trial Unit (ECTU), Bavarian Cancer Research Center, National Center for Tumor Diseases, Comprehensive Cancer Center Mainfranken and University Hospital Würzburg, Würzburg, Germany. [Champiat S] Department of Therapeutic Innovation and Early Phase Trials, Gustave Roussy, Villejuif, France. [Olmedo ME] Department of Medical Oncology, Ramon y Cajal University Hospital, Madrid, Spain. [Boyer M] Department of Medical Oncology, Chris O’Brien Lifehouse, Sydney, Australia. Faculty of Medicine and Health, School of Medicine, University of Sydney, Sydney, Australia. [He H] Comprehensive Cancer Center, Pelotonia Institute for ImmunoOncology, The Ohio State University, Columbus, OH. [Felip E] Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid39208379
dc.identifier.wos001328849800006
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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