Publication:
Potential Survival Benefit for Patients Receiving Allogeneic Hematopoietic Stem Cell Transplantation after Nivolumab Therapy for Relapse/Refractory Hodgkin Lymphoma: Real-Life Experience in Spain.

dc.contributor.authorMartínez, Carmen
dc.contributor.authorCarpio, Cecilia
dc.contributor.authorHeras, Inmaculada
dc.contributor.authorRíos-Herranz, Eduardo
dc.contributor.authorBuch, Joan
dc.contributor.authorGutierrez, Antonio
dc.contributor.authorRomero, Samuel
dc.contributor.authorZeberio, Izaskun
dc.contributor.authorGarcía-García, Irene
dc.contributor.authorRodriguez-Izquierdo, Antonia
dc.contributor.authorAlonso, Rosalía
dc.contributor.authorBargay, Joan
dc.contributor.authorBarrenetxea, Cristina
dc.contributor.authorDomingo-Doménech, Eva
dc.contributor.authorde Haro, Manuel Espeso
dc.contributor.authorPalomera, Luis
dc.contributor.authorGarcía-Sanz, Ramón
dc.contributor.authorSpanish Group of Lymphoma and Bone Marrow Transplantation (GELTAMO)
dc.date.accessioned2023-02-08T14:41:28Z
dc.date.available2023-02-08T14:41:28Z
dc.date.issued2020-02-14
dc.description.abstractClinical trials have shown that nivolumab has remarkable activity against relapsed/refractory classical Hodgkin lymphoma (cHL). However, the role of allogeneic hematopoietic stem cell transplantation (allo-HSCT) as consolidation therapy in these patients remains controversial. We performed a retrospective analysis of data from 74 patients treated with nivolumab. The overall response rate was 58% (including 30.6% with complete responses). Treatment-related adverse events were reported in 56.8% of patients (grade ≥3 in 9.4%). The main reasons for nivolumab discontinuation were referral for transplantation (41.7% patients) and disease progression (37.5%). The 2-year overall survival (OS) rate was 52% for the entire series. Ultimately, 39 patients underwent allo-HSCT. The cumulative incidence of grade II-IV acute graft-versus-host disease was 33.3% (grade III-IV in 2 patients). The cumulative incidence of nonrelapse mortality was 13.2%. Among the patients who responded to nivolumab, the 2-year OS and progression-free survival (PFS) were higher in patients who underwent consolidation with allo-HSCT (77.5% versus 42.6% [P = .126] and 73.9% versus 27.2% [P = .025], respectively). Thus, the efficacy and safety of nivolumab were comparable to values reported in previous clinical trials. The percentage of patients who bridged to transplantation was high, indicating a preference for Spanish physicians. These results suggest that consolidation allo-HSCT increases OS and PFS.
dc.identifier.doi10.1016/j.bbmt.2020.02.003
dc.identifier.essn1523-6536
dc.identifier.pmid32068094
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.bbmt.2020.02.003
dc.identifier.urihttp://hdl.handle.net/10668/15119
dc.issue.number8
dc.journal.titleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
dc.journal.titleabbreviationBiol Blood Marrow Transplant
dc.language.isoen
dc.organizationHospital Universitario Regional de Málaga
dc.organizationÁrea de Gestión Sanitaria Sur de Sevilla
dc.organizationAGS - Sur de Sevilla
dc.page.number1534-1542
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAllogeneic transplantation
dc.subjectHodgkin lymphoma
dc.subjectNivolumab
dc.subjectRelapsed/refractory lymphoma
dc.subject.meshDisease-Free Survival
dc.subject.meshGraft vs Host Disease
dc.subject.meshHematopoietic Stem Cell Transplantation
dc.subject.meshHodgkin Disease
dc.subject.meshHumans
dc.subject.meshNeoplasm Recurrence, Local
dc.subject.meshNivolumab
dc.subject.meshRetrospective Studies
dc.subject.meshSpain
dc.titlePotential Survival Benefit for Patients Receiving Allogeneic Hematopoietic Stem Cell Transplantation after Nivolumab Therapy for Relapse/Refractory Hodgkin Lymphoma: Real-Life Experience in Spain.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number26
dspace.entity.typePublication

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