Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study

dc.contributor
Institut Català de la Salut
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[Vahdat LT] Weill Cornell Medicine, New York, NY, USA. [Schmid P] Center for Experimental Cancer Medicine, Barts Cancer Institute, London, UK. [Forero-Torres A] University of Alabama School of Medicine, Birmingham, AL, USA. [Blackwell K] Duke University Medical Center, Durham, NC, USA. [Telli ML] Stanford University School of Medicine, Stanford, CA, USA. [Melisko M] University of California, San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, CA, USA. [Cortes J] IOB Institute of Oncology, Quironsalud Group, Madrid & Barcelona. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
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Vall d'Hebron Barcelona Hospital Campus
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Vahdat, Linda T.
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Forero-Torres, Andres
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Blackwell, Kimberly
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Telli, Melinda L.
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Melisko, Michelle
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Cortés Castan, Javier
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Schmid, Peter
dc.date.accessioned
2025-10-25T05:39:27Z
dc.date.available
2025-10-25T05:39:27Z
dc.date.issued
2022-02-22T11:26:34Z
dc.date.issued
2022-02-22T11:26:34Z
dc.date.issued
2021-05-20
dc.identifier
Vahdat LT, Schmid P, Forero-Torres A, Blackwell K, Telli ML, Melisko M, et al. Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study. NPJ Breast Cancer. 2021 May 20;7:57.
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2374-4677
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https://hdl.handle.net/11351/7063
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10.1038/s41523-021-00244-6
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34016993
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000657821100002
dc.identifier.uri
http://hdl.handle.net/11351/7063
dc.description.abstract
Breast cancer; Cancer
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Càncer de mama; Càncer
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Cáncer de mama; Cáncer
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The METRIC study (NCT#0199733) explored a novel antibody–drug conjugate, glembatumumab vedotin (GV), targeting gpNMB that is overexpressed in ~40% of patients with triple-negative breast cancer (TNBC) and associated with poor prognosis. The study was a randomized, open-label, phase 2b study that evaluated progression-free survival (PFS) of GV compared with capecitabine in gpNMB-overexpressing TNBC. Patients who had previously received anthracycline and taxane-based therapy were randomized 2:1 to receive, GV (1.88 mg/kg IV q21 days) or capecitabine (2500 mg/m2 PO daily d1–14 q21 days). The primary endpoint was RECIST 1.1 PFS per independent, blinded central review. In all, 327 patients were randomized to GV (213 treated) or capecitabine (92 treated). Median PFS was 2.9 months for GV vs. 2.8 months for capecitabine. The most common grade ≥3 toxicities for GV were neutropenia, rash, and leukopenia, and for capecitabine were fatigue, diarrhea, and palmar-plantar erythrodysesthesia. The study did not meet the primary endpoint of improved PFS over capecitabine or demonstrate a relative risk/benefit improvement over capecitabine.
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Funding provided by Celldex Therapeutics, Inc.
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application/pdf
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application/pdf
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application/pdf
dc.language
eng
dc.publisher
Nature Research
dc.relation
NPJ Breast Cancer;7
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https://doi.org/10.1038/s41523-021-00244-6
dc.rights
Attribution 4.0 International
dc.rights
http://creativecommons.org/licenses/by/4.0/
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info:eu-repo/semantics/openAccess
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Scientia
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Mama - Càncer - Tractament
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Metàstasi
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Avaluació de resultats (Assistència sanitària)
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DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms::Triple Negative Breast Neoplasms
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Other subheadings::Other subheadings::Other subheadings::/drug therapy
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DISEASES::Neoplasms::Neoplastic Processes::Neoplasm Metastasis
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ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Diagnosis::Prognosis::Treatment Outcome
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ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama::neoplasias de mama triple negativos
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Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia
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ENFERMEDADES::neoplasias::procesos neoplásicos::metástasis neoplásica
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TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::diagnóstico::pronóstico::resultado del tratamiento
dc.title
Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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