Publication: PD-L1 testing based on the SP142 antibody in metastatic triple-negative breast cancer: summary of an expert round-table discussion.
dc.contributor.author | Peg, Vicente | |
dc.contributor.author | López-García, María Ángeles | |
dc.contributor.author | Comerma, Laura | |
dc.contributor.author | Peiró, Gloria | |
dc.contributor.author | García-Caballero, Tomás | |
dc.contributor.author | López, Ángel Concha | |
dc.contributor.author | Suárez-Gauthier, Ana | |
dc.contributor.author | Ruiz, Irune | |
dc.contributor.author | Rojo, Federico | |
dc.date.accessioned | 2023-02-09T10:38:07Z | |
dc.date.available | 2023-02-09T10:38:07Z | |
dc.date.issued | 2020-12-08 | |
dc.description.abstract | Triple-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 TNBC. | |
dc.identifier.doi | 10.2217/fon-2020-1100 | |
dc.identifier.essn | 1744-8301 | |
dc.identifier.pmid | 33289433 | |
dc.identifier.unpaywallURL | https://doi.org/10.2217/fon-2020-1100 | |
dc.identifier.uri | http://hdl.handle.net/10668/16754 | |
dc.issue.number | 10 | |
dc.journal.title | Future oncology (London, England) | |
dc.journal.titleabbreviation | Future Oncol | |
dc.language.iso | en | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.page.number | 1209-1218 | |
dc.pubmedtype | Journal Article | |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | PD-L1 | |
dc.subject | antibody | |
dc.subject | breast cancer | |
dc.subject | diagnosis | |
dc.subject | immunohistochemistry | |
dc.subject | immunotherapy | |
dc.subject.mesh | Antibodies, Monoclonal | |
dc.subject.mesh | B7-H1 Antigen | |
dc.subject.mesh | Biomarkers, Tumor | |
dc.subject.mesh | Clinical Decision-Making | |
dc.subject.mesh | Disease Management | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Immunohistochemistry | |
dc.subject.mesh | Molecular Targeted Therapy | |
dc.subject.mesh | Neoplasm Metastasis | |
dc.subject.mesh | Neoplasm Staging | |
dc.subject.mesh | Triple Negative Breast Neoplasms | |
dc.title | PD-L1 testing based on the SP142 antibody in metastatic triple-negative breast cancer: summary of an expert round-table discussion. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 17 | |
dspace.entity.type | Publication |