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dc.contributor.authorAbrisqueta, Pau
dc.contributor.authorGonzález-Barca, Eva
dc.contributor.authorFerrà, Christelle
dc.contributor.authorRíos-Herranz, Eduardo
dc.contributor.authorFernández de la Mata, Margarita
dc.contributor.authorDelgado, Julio
dc.contributor.authorAndreu, Rafael
dc.contributor.authorHernández-Rivas, José Ángel
dc.contributor.authorTerol, María José
dc.contributor.authorNavarro, Almudena
dc.contributor.authorVidriales, M. Belén
dc.contributor.authorBaltasar, Patricia
dc.contributor.authorSerna, Javier de la
dc.contributor.authorRamírez, Ángel
dc.contributor.authorBallester, Carmen
dc.contributor.authorMoreno, Carol
dc.contributor.authorGarcía-Marco, José Antonio
dc.contributor.authorCórdoba, Raúl
dc.contributor.authorYáñez San Segundo, Lucrecia 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-09-16T15:01:56Z
dc.date.available2024-09-16T15:01:56Z
dc.date.issued2024
dc.identifier.issn2589-5370
dc.identifier.urihttps://hdl.handle.net/10902/33814
dc.description.abstractBackground: BTK inhibitors have been concurrently administered with anti-CD20 monoclonal antibodies (mAbs) in chronic lymphocytic leukemia (CLL). However, the optimal regimen for combining these two drugs remains pending. Methods: This multi-center phase 2 study aimed to analyze whether consolidation with ofatumumab improved the response in patients with CLL receiving front-line treatment with ibrutinib. Patients received 12 cycles of ibrutinib monotherapy. Those who achieved CR after this induction were maintained on ibrutinib. Conversely, those who did not attain CR continued with ibrutinib in addition to a consolidation, which involved 7 doses of ofatumumab. The primary objective was the complete response (CR) rate at cycle 20. This study is registered within the EU Clinical Trials Register (EudraCT 2016-004937-26). Findings: Between September 8, 2017, and May 21, 2018, 84 patients (median age, 69 years) were included. After completion of 12 cycles of ibrutinib (n = 80), 4 patients (5%) were in CR, 67 (84%) in partial response (PR), and 6 patients (7%) had a PR with lymphocytosis (PRL). After consolidation with ofatumumab, 20 patients improved the response from PR to CR and 6 patients with PRL obtained a PR. Seventy-one patients (85%) completed 20 cycles of treatment, with a CR rate of 24/71 (34%). According to the intention-to-treat analysis at cycle 20, the ORR was 69/84 (82.2%), with a CRR of 24/84 (28.6%). Progression-free survival and overall survival at 48-months were 89.9% (CI: 82.4?95.5) and 92.2% (CI: 85.3?97.1), respectively. Interpretation: These findings underscore the potential for a consolidation strategy in CLL, wherein the addition of a mAb in patients with low tumor burden might enhance the quality of the response.es_ES
dc.description.sponsorshipFunding: The study was funded by Janssen that also supplied ibrutinib, whereas ofatumumab was supplied by Novartis. Acknowledgements: The authors thank the patients for their participation. The study was funded by Janssen that also supplied ibrutinib, whereas ofatumumab was supplied by Novartis. This work was also supported in part by the Instituto de Salud Carlos III, Fondo de Investigaciones Sanitarias (PI17/00943, PI18/01392, PI22/01204), Gilead Sciences (GLD15/00348, M.G) and the Health Council of the Junta de Castilla y León (GRS 2036/A/19, M.G.).es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rights© 2024 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license.es_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceeClinicalMedicine, 2024, 73, 102642es_ES
dc.subject.otherChronic lymphocytic leukemiaes_ES
dc.subject.otherTreatmentes_ES
dc.subject.otherConsolidationes_ES
dc.titleIbrutinib followed by ofatumumab consolidation in previously untreated patients with chronic lymphocytic leukemia (CLL): GELLC-7 trial from the Spanish group of CLL (GELLC)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.eclinm.2024.102642es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.eclinm.2024.102642
dc.type.versionpublishedVersiones_ES


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© 2024 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license.Excepto si se señala otra cosa, la licencia del ítem se describe como © 2024 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license.