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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorMiyoshi, Yasuo
dc.contributor.authorYoshimura, Yuta
dc.contributor.authorSaito, Kenichi
dc.contributor.authorMuramoto, Kenzo
dc.contributor.authorSugawara, Michiko
dc.contributor.authorAlexis, Karenza
dc.contributor.authorCortés Castan, Javier
dc.date.accessioned2021-09-16T08:31:26Z
dc.date.available2021-09-16T08:31:26Z
dc.date.issued2020-07
dc.identifier.citationMiyoshi Y, Yoshimura Y, Saito K, Muramoto K, Sugawara M, Alexis K, et al. High absolute lymphocyte counts are associated with longer overall survival in patients with metastatic breast cancer treated with eribulin—but not with treatment of physician’s choice—in the EMBRACE study. Breast Cancer. 2020 Jul;27:706–715.
dc.identifier.issn1880-4233
dc.identifier.urihttps://hdl.handle.net/11351/6325
dc.descriptionEribulin; Metastatic breast cancer; Overall survival
dc.description.abstractBackground Eribulin, a nontaxane synthetic inhibitor of microtubule dynamics, is widely used to manage locally advanced or metastatic breast cancer (MBC). Eribulin has demonstrated immunomodulatory activity on the tumour microenvironment. Baseline neutrophil-to-lymphocyte ratio (NLR), a marker of immune status, may predict progression-free survival in eribulin treatment. This post hoc analysis assessed predictors for overall survival (OS). Methods The phase 3 open-label study (EMBRACE) of eribulin versus treatment of physician’s choice (TPC) in patients with MBC provided source data. Baseline absolute lymphocyte counts (ALCs) and NLR were evaluable in 751 and 713 patients, respectively. Results Eribulin prolonged OS versus TPC in patients with baseline ALC ≥ 1500/µl (hazard ratio [HR] 0.586; 95% confidence interval [CI] 0.437–0.784; P < 0.001). There was no significant difference by treatment for ALC < 1500/µl (HR 1.002; 95% CI 0.800–1.253; P = 0.989). Univariate and multivariate analyses were performed and identified baseline ALC as a potential predictor of OS in eribulin-treated patients. Interaction analysis of OS supported 1500/µl as a potentially differential cutoff value. NLR at a cutoff value of 3 was associated with prolonged OS (eribulin group). However, similar results were also observed in the TPC group, without apparent interaction effect, suggesting that NLR may be a general prognostic marker rather than a specific predictor of OS for eribulin. Discussion This hypothesis-generating study speculates that baseline ALC may be an independent predictor for longer OS in eribulin-treated MBC patients and could be clinically impactful because it can be evaluated without the need for additional invasive procedures.
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofseriesBreast Cancer;27
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectMama - Càncer - Tractament
dc.subjectAnàlisi de supervivència (Biometria)
dc.subject.meshBreast Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshProgression-Free Survival
dc.titleHigh absolute lymphocyte counts are associated with longer overall survival in patients with metastatic breast cancer treated with eribulin—but not with treatment of physician’s choice—in the EMBRACE study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1007/s12282-020-01067-2
dc.subject.decsneoplasias de la mama
dc.subject.decs/farmacoterapia
dc.subject.decssupervivencia libre de progresión
dc.relation.publishversionhttps://doi.org/10.1007/s12282-020-01067-2
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Miyoshi Y] Department of Surgery, Division of Breast and Endocrine Surgery, Hyogo College of Medicine, Mukogawa-cho 1-1, Nishinomiya, Hyogo 663-8501, Japan. [Yoshimura Y, Muramoto K, Sugawara M] Eisai Co., Ltd., Koishikawa, Bunkyo-ku, Tokyo, Japan. [Saito K, Alexis K] Eisai Inc., Woodclif Lake, NJ, USA. [Cortes J] IOB Institute of Oncology, Quironsalud Group, Madrid, Barcelona, Spain. Breast Cancer Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.identifier.pmid32133606
dc.identifier.wos000544235400019
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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