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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorBhatia, Shailender
dc.contributor.authorTopalian, Suzanne
dc.contributor.authorSharfman, William
dc.contributor.authorMeyer, Tim
dc.contributor.authorSteven, Neil
dc.contributor.authorLao, Christopher D.
dc.contributor.authorFariñas-Madrid, Lorena
dc.date.accessioned2025-03-21T09:17:05Z
dc.date.available2025-03-21T09:17:05Z
dc.date.issued2025-03-20
dc.identifier.citationBhatia S, Topalian SL, Sharfman W, Meyer T, Steven N, Lao CD, et al. Nivolumab With or Without Ipilimumab in Patients With Recurrent or Metastatic Merkel Cell Carcinoma: A Nonrandomized, Open-Label, International, Multicenter Phase I/II Study. J Clin Oncol. 2025 Mar 20;43(9):1137–47.
dc.identifier.issn1527-7755
dc.identifier.urihttp://hdl.handle.net/11351/12809
dc.descriptionNivolumab; Merkel cell carcinoma; Metastasis
dc.description.abstractPurpose Approximately 50% of patients with advanced Merkel cell carcinoma (MCC) have primary or acquired resistance to PD-(L)1 blockade, which may be overcome using combination immune checkpoint inhibition (ICI) with anti–cytotoxic T lymphocyte antigen-4 antibody. We present results from the recurrent/metastatic MCC cohort in CheckMate 358, a nonrandomized, multicohort, phase I/II study of nivolumab (NIVO) with or without ipilimumab (IPI) in virus-associated cancers (ClinicalTrials.gov identifier: NCT02488759). Methods ICI-naïve patients with recurrent/metastatic MCC and 0-2 previous systemic therapies were administered NIVO monotherapy at 240 mg once every 2 weeks or combination therapy with NIVO 3 mg/kg once every 2 weeks + IPI 1 mg/kg once every 6 weeks. The primary end point was objective response. Secondary end points included duration of response (DOR), progression-free survival (PFS), and overall survival (OS). Results Sixty-eight patients received NIVO (n = 25) or NIVO + IPI (n = 43). The objective response rate (95% CI) and median DOR (95% CI), respectively, were 60% (38.7 to 78.9) and 60.6 months (16.7 to not applicable [NA]) with NIVO and 58% (42.1 to 73) and 25.9 months (10.4 to NA) with NIVO + IPI. The median PFS (95% CI) and OS (95% CI), respectively, were 21.3 (9.2 to 62.5) and 80.7 (23.3 to NA) months with NIVO and 8.4 (3.7 to 24.3) and 29.8 (8.5 to 48.3) months with NIVO + IPI. The incidence of grade 3/4 treatment-related adverse events was 28% with NIVO and 47% with the combination. Conclusion This nonrandomized study showed frequent and durable responses with both NIVO and NIVO + IPI in patients with ICI-naïve advanced MCC. However, it did not show improvement in efficacy with the combination, thus contradicting previous study reports that had suggested clinical benefit with combination ICI. A randomized trial of NIVO + IPI versus NIVO monotherapy is warranted.
dc.language.isoeng
dc.publisherAmerican Society of Clinical Oncology
dc.relation.ispartofseriesJournal of Clinical Oncology;43(9)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectPell - Càncer - Tractament
dc.subjectMedicaments antineoplàstics - Ús terapèutic - Efectes secundaris
dc.subjectQuimioteràpia combinada
dc.subjectAnticossos monoclonals - Ús terapèutic - Efectes secundaris
dc.subjectPell - Càncer - Recaiguda
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshAntineoplastic Agents, Immunological
dc.subject.mesh/adverse effects
dc.subject.meshNeoplasm Recurrence, Local
dc.subject.meshCarcinoma, Merkel Cell
dc.subject.mesh/drug therapy
dc.subject.meshSkin Neoplasms
dc.subject.meshProgression-Free Survival
dc.titleNivolumab With or Without Ipilimumab in Patients With Recurrent or Metastatic Merkel Cell Carcinoma: A Nonrandomized, Open-Label, International, Multicenter Phase I/II Study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1200/JCO-24-02138
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decsinmunoterapia antineoplásica
dc.subject.decs/efectos adversos
dc.subject.decsrecurrencia neoplásica local
dc.subject.decscarcinoma de células de Merkel
dc.subject.decs/farmacoterapia
dc.subject.decsneoplasias cutáneas
dc.subject.decssupervivencia libre de progresión
dc.relation.publishversionhttps://doi.org/10.1200/JCO-24-02138
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Bhatia S] Division of Hematology-Oncology, University of Washington and Fred Hutchinson Cancer Center, Seattle, WA. [Topalian SL, Sharfman W] Division of Hematology-Oncology, University of Washington and Fred Hutchinson Cancer Center, Seattle, WA. Johns Hopkins Bloomberg-Kimmel Institute for Cancer Immunotherapy and Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD. [Meyer T] Department of Oncology, University College London Cancer Institute, London, United Kingdom. [Steven N] Institute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom. [Lao CD] Michigan Medicine, Rogel Cancer Center, Ann Arbor, MI. [Fariñas-Madrid L] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.identifier.pmid39889250
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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