PD-L1 testing based on the SP142 antibody in metastatic triple-negative breast cancer: summary of an expert round-table discussion

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Ciencias Morfolóxicasgl
dc.contributor.authorPeg, Vicente
dc.contributor.authorLópez García, María Ángeles
dc.contributor.authorComerma, Laura
dc.contributor.authorPeiró, Gloria
dc.contributor.authorGarcía-Caballero Parada, Tomás
dc.contributor.authorConcha López, Ángel
dc.contributor.authorSuárez Gauthier, Ana
dc.contributor.authorRuiz, Irune
dc.contributor.authorRojo, Federico
dc.date.accessioned2021-03-18T09:30:22Z
dc.date.available2021-03-18T09:30:22Z
dc.date.issued2021
dc.description.abstractTriple-negative breast cancer (TNBC) is more aggressive than other breast cancer subtypes. TNBC is characterized by increased expression of Programmed Death-ligand 1 (PD-L1), a signal used by many tumors to escape the immune response. Expression of PD-L1 is a positive predictor of response to immunotherapy; therefore, it should be investigated in TNBC in order to select patients who may benefit from anti-PD-L1 therapies. While many PD-L1 assays are available, only the VENTANA platform with the anti-PD-L1 (SP142) antibody is licensed as a companion diagnostic device for selecting patients with metastatic/advanced TNBC who are candidates for treatment with atezolizumab. In this article, we provide a summary of an expert round-table discussion about PD-L1 testing, using the SP142 antibody in metastatic TNBCgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThis article was funded by Roche Diagnostics S.L. The present work was supported by grants from the Spanish Ministry of Economy and Competitiveness (MINECO) with European Regional Development Fund (ERDF) funding through the Institute of Health Carlos III (AES Program, PI15/00934; CIBERONC, Biomedical Research Networking Centre for Cancer). V Peg has received grants from Roche; held advisory roles for Roche, MSD and AstraZeneca and has received honoraria from Sysmex Spaingl
dc.identifier.citationFuture Oncology 2021 17:10, 1209-1218. https://doi.org/10.2217/fon-2020-1100gl
dc.identifier.doi10.2217/fon-2020-1100
dc.identifier.essn1744-8301
dc.identifier.issn1479-6694
dc.identifier.urihttp://hdl.handle.net/10347/24826
dc.language.isoenggl
dc.publisherFuture Medicinegl
dc.relation.publisherversionhttps://doi.org/10.2217/fon-2020-1100gl
dc.rights© 2021 Federico Rojo (on behalf of all co-authors). This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/gl
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAntibodygl
dc.subjectBreast cancergl
dc.subjectDiagnosisgl
dc.subjectImmunohistochemistrygl
dc.subjectImmunotherapygl
dc.subjectPD-L1gl
dc.titlePD-L1 testing based on the SP142 antibody in metastatic triple-negative breast cancer: summary of an expert round-table discussiongl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublicationf825b64a-9678-43c6-8c1d-6a943ec91adb
relation.isAuthorOfPublication.latestForDiscoveryf825b64a-9678-43c6-8c1d-6a943ec91adb

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