Publication: Real-life efficacy of immunotherapy for Sézary syndrome: a multicenter observational cohort study.
| cris.virtualsource.author-orcid | 85887c8e-aed9-4780-b1c0-931345a5c52e | |
| cris.virtualsource.author-orcid | 1e4ed692-411d-4da7-9eeb-2094a0768179 | |
| datacite.rights | open.access | |
| dc.contributor.author | Bozonnat, Alizée | |
| dc.contributor.author | Beylot-Barry, Marie | |
| dc.contributor.author | Dereure, Olivier | |
| dc.contributor.author | D'Incan, Michel | |
| dc.contributor.author | Quereux, Gaëlle | |
| dc.contributor.author | Guenova, Emmanuella | |
| dc.contributor.author | Perier-Muzet, Marie | |
| dc.contributor.author | Dalle, Stephane | |
| dc.contributor.author | Grange, Florent | |
| dc.contributor.author | Viguier, Manuelle-Anne | |
| dc.contributor.author | Ram-Wolff, Caroline | |
| dc.contributor.author | Feldmeyer, Laurence | |
| dc.contributor.author | Beltraminelli, Helmut | |
| dc.contributor.author | Bonnet, Nathalie | |
| dc.contributor.author | Amatore, Florent | |
| dc.contributor.author | Maubec, Eve | |
| dc.contributor.author | Franck, Nathalie | |
| dc.contributor.author | Machet, Laurent | |
| dc.contributor.author | Chasset, François | |
| dc.contributor.author | Brunet-Possenti, Florence | |
| dc.contributor.author | Bouaziz, Jean-David | |
| dc.contributor.author | Battistella, Maxime | |
| dc.contributor.author | Donzel, Marie | |
| dc.contributor.author | Pham-Ledard, Anne | |
| dc.contributor.author | Bejar, Claudia | |
| dc.contributor.author | Moins-Teisserenc, Hélène | |
| dc.contributor.author | Mourah, Samia | |
| dc.contributor.author | Saiag, Philippe | |
| dc.contributor.author | Hainaut, Ewa | |
| dc.contributor.author | Michel, Catherine | |
| dc.contributor.author | Bens, Guido | |
| dc.contributor.author | Adamski, Henri | |
| dc.contributor.author | Aubin, François | |
| dc.contributor.author | Boulinguez, Serge | |
| dc.contributor.author | Joly, Pascal | |
| dc.contributor.author | Tedbirt, Billal | |
| dc.contributor.author | Templier, Isabelle | |
| dc.contributor.author | Troin, Laura | |
| dc.contributor.author | Montaudié, Henri | |
| dc.contributor.author | Ingen-Housz-Oro, Saskia | |
| dc.contributor.author | Faiz, Sarah | |
| dc.contributor.author | Mortier, Laurent | |
| dc.contributor.author | Dobos, Gabor | |
| dc.contributor.author | Bagot, Martine | |
| dc.contributor.author | Resche-Rigon, Matthieu | |
| dc.contributor.author | Montlahuc, Claire | |
| dc.contributor.author | Serret-Larmande, Arnaud | |
| dc.contributor.author | de Masson, Adèle | |
| dc.date.accessioned | 2024-10-26T18:32:48Z | |
| dc.date.available | 2024-10-26T18:32:48Z | |
| dc.date.issued | 2024-07 | |
| dc.description.abstract | BACKGROUND Sézary syndrome is an extremely rare and fatal cutaneous T-cell lymphoma (CTCL). Mogamulizumab, an anti-CCR4 monoclonal antibody, has recently been associated with increased progression-free survival in a randomized clinical trial in CTCL. We aimed to evaluate OS and prognostic factors in Sézary syndrome, including treatment with mogamulizumab, in a real-life setting. METHODS Data from patients with Sézary (ISCL/EORTC stage IV) and pre-Sézary (stage IIIB) syndrome diagnosed from 2000 to 2020 were obtained from 24 centers in Europe. Age, disease stage, plasma lactate dehydrogenases levels, blood eosinophilia at diagnosis, large-cell transformation and treatment received were analyzed in a multivariable Cox proportional hazard ratio model. This study has been registered in ClinicalTrials (SURPASSe01 study: NCT05206045). FINDINGS Three hundred and thirty-nine patients were included (58% men, median age at diagnosis of 70 years, Q1-Q3, 61-79): 33 pre-Sézary (9.7% of 339), 296 Sézary syndrome (87.3%), of whom 10 (2.9%) had large-cell transformation. One hundred and ten patients received mogamulizumab. Median follow-up was 58 months (95% confidence interval [CI], 53-68). OS was 46.5% (95% CI, 40.6%-53.3%) at 5 years. Multivariable analysis showed that age ≥ 80 versus <50 (HR: 4.9, 95% CI, 2.1-11.2, p = 0.001), and large-cell transformation (HR: 2.8, 95% CI, 1.6-5.1, p = 0.001) were independent and significant factors associated with reduced OS. Mogamulizumab treatment was significantly associated with decreased mortality (HR: 0.34, 95% CI, 0.15-0.80, p = 0.013). INTERPRETATION Treatment with mogamulizumab was significantly and independently associated with decreased mortality in Sézary syndrome. FUNDING French Society of Dermatology, Swiss National Science Foundation (IZLIZ3_200253/1) and SKINTEGRITY.CH collaborative research program. | |
| dc.description.sponsorship | Universitätsklinik für Dermatologie | |
| dc.identifier.doi | 10.48350/199015 | |
| dc.identifier.pmid | 39007062 | |
| dc.identifier.publisherDOI | 10.1016/j.eclinm.2024.102679 | |
| dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/179161 | |
| dc.language.iso | en | |
| dc.publisher | Elsevier | |
| dc.relation.ispartof | EClinicalMedicine | |
| dc.relation.issn | 2589-5370 | |
| dc.relation.organization | Clinic of Dermatology | |
| dc.relation.url | https://doi.org/10.48620/84960 | |
| dc.subject | Cutaneous T-cell lymphoma Immunotherapy Mogamulizumab Monoclonal antibody Sézary syndrome | |
| dc.subject.ddc | 600 - Technology::610 - Medicine & health | |
| dc.title | Real-life efficacy of immunotherapy for Sézary syndrome: a multicenter observational cohort study. | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| dspace.file.type | text | |
| oaire.citation.issue | 102679 | |
| oaire.citation.volume | 73 | |
| oairecerif.author.affiliation | Universitätsklinik für Dermatologie | |
| oairecerif.author.affiliation | Universitätsklinik für Dermatologie | |
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| unibe.date.licenseChanged | 2024-07-16 13:30:52 | |
| unibe.description.ispublished | pub | |
| unibe.eprints.legacyId | 199015 | |
| unibe.refereed | true | |
| unibe.subtype.article | journal |
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