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dc.contributor.authorHermans, Sjoerd J. F.
dc.contributor.authorVersluis, Jurjen
dc.contributor.authorvan Werkhoven, Erik D.
dc.contributor.authorvan Norden, Yvette
dc.contributor.authorJanssen, Jeroen J. W. M.
dc.contributor.authorHuls, Gerwin A.
dc.contributor.authorPabst, Thomas
dc.contributor.authorBreems, Dimitri A.
dc.contributor.authorBerkx, Elizabeth
dc.contributor.authorDinmohamed, Avinash G.
dc.contributor.authorHuijgens, Peter C.
dc.contributor.authorSträng, Eric
dc.contributor.authorHernández Rivas, Jesús María 
dc.contributor.authorSobas, Marta
dc.contributor.authorAyala Diaz, Rosa
dc.contributor.authorMartínez López, Joaquín
dc.contributor.authorMetzeler, Klaus H.
dc.contributor.authorHaferlach, Torsten
dc.contributor.authorThiede, Christian
dc.contributor.authorUyl-de Groot, Carin A.
dc.contributor.authorBullinger, Lars
dc.contributor.authorLöwenberg, Bob
dc.contributor.authorOssenkoppele, Gert J.
dc.contributor.authorPignatti, Francesco
dc.contributor.authorCornelissen, Jan J.
dc.date.accessioned2026-07-02T10:46:45Z
dc.date.available2026-07-02T10:46:45Z
dc.date.issued2026-01
dc.identifier.citationHermans, S. J. F., Versluis, J., Van Werkhoven, E. D., Van Norden, Y., Janssen, J. J. W. M., Huls, G. A., Pabst, T., Breems, D. A., Berkx, E., Dinmohamed, A. G., Huijgens, P. C., Sträng, E., Hernández Rivas, J. M., Sobas, M., Ayala Diaz, R., Martinez Lopez, J., Metzeler, K. H., Haferlach, T., Thiede, C., … Cornelissen, J. J. (2026). Comparability of external and internal control patients for the prospective randomized HOVON ‐103 trial in older AML patients. British Journal of Haematology, 208(1), 179-188. https://doi.org/10.1111/bjh.20185es_ES
dc.identifier.urihttp://hdl.handle.net/10366/172037
dc.description.abstract[EN]Real-world data (RWD) previously contributed to post-marketing regulatory decision-making, but are currently also considered as external controls to single-arm trials. The use of RWD control data may be compromised by methodological issues, urging validation of RWD control cohorts. Two external control cohorts of newly diagnosed acute myeloid leukaemia patients, one registered by the HARMONY Alliance (HA) and one by the Netherlands Cancer Registry (NCR), were compared to the control arm of the randomized HOVON-103 trial (H103 controls). All patients, aged >65 years with a WHO performance score of 0-2 (or missing), received standard induction chemotherapy. 1:1 propensity score calliper matching (PSM) was applied to improve comparability, and overall (OS) and relapse-free survival (RFS) were assessed. Fewer data elements were available in external cohorts compared to H103 controls, specifically in the NCR cohort. Baseline characteristics of the external cohorts differed from H103 controls; missing data were also more frequent and predominantly concerned WHO performance score. After PSM, HA patients demonstrated non-significantly different OS and RFS to H103 controls at 2 years (26 ± 4% vs. 31 ± 5%, p = 0.59; 24 ± 5% vs. 30 ± 6%, p = 0.52), while NCR patients had 12% lower OS (28 ± 4% vs. 40 ± 4%, p = 0.21). Validation of external control cohorts is needed before incorporating RWD control data into comparative analyses, as missing data, specifically comorbidities, and residual confounding may limit comparability.es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relation.ispartofseries25GMO;5
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/es_ES
dc.subjectLeukemia, Myeloid, Acutees_ES
dc.subjectAntineoplastic Combined Chemotherapy Protocolses_ES
dc.subjectHumanses_ES
dc.subjectAgedes_ES
dc.subjectMalees_ES
dc.subjectFemalees_ES
dc.subjectAged, 80 and overes_ES
dc.subjectProspective Studieses_ES
dc.subjectRegistrieses_ES
dc.subject.meshAged, 80 and over *
dc.subject.meshAged *
dc.subject.meshProspective Studies *
dc.subject.meshLeukemia, Myeloid, Acute *
dc.subject.meshHumans *
dc.subject.meshRegistries *
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols *
dc.titleComparability of external and internal control patients for the prospective randomized HOVON-103 trial in older AML patientses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1111/bjh.20185es_ES
dc.identifier.doi10.1111/bjh.20185
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid40419286
dc.identifier.essn1365-2141
dc.journal.titleBritish journal of haematologyes_ES
dc.volume.number208es_ES
dc.issue.number1es_ES
dc.page.initial179es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsancianos de 80 o más años *
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada *
dc.subject.decshumanos *
dc.subject.decsanciano *
dc.subject.decssistema de registros *
dc.subject.decsleucemia mieloide aguda *
dc.subject.decsestudios prospectivos *


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