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


Por: Peg, V, Lopez-Garcia, M, Comerma, L, Peiro, G, Garcia-Caballero, T, Lopez, A, Suarez-Gauthier, A, Ruiz, I and Rojo, F

Publicada: 1 abr 2021 Ahead of Print: 1 dic 2020
Resumen:
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. Lay abstract Triple negative breast cancer (TNBC) is the most aggressive breast cancer subtype. Recent discoveries in TNBC have shown that the higher the expression of the surface molecule PD-L1 in the cancer cells, the better the response of patients to immunotherapy. While several tests or diagnostics assays for detecting PD-L1 exist, only the antibody anti-PD-L1 SP142 possesses proven diagnostic value for selecting metastatic TNBC patients eligible for atezolizumab immunotherapy. Throughout the present article, a group of experts discusses how to best carry out the assessment of PD-L1 status with this assay.

Filiaciones:
Peg, V:
 Vall dHebron Hosp Univ, Dept Anat Patol, Barcelona Hosp Campus, Barcelona, Spain

 Vall dHebron Inst Recerca VHIR, Grp Patol Mol, Barcelona, Spain

 Inst Salud Carlos III, Ctr Invest Biomed Red Canc CIBERONC, Madrid, Spain

 Univ Autonoma Barcelona, Bellaterra, Spain

Lopez-Garcia, M:
 Inst Salud Carlos III, Ctr Invest Biomed Red Canc CIBERONC, Madrid, Spain

 Hosp Univ Virgen del Rocio, Serv Anat Patol, Seville, Spain

Comerma, L:
 Hosp del Mar, Dept Anat Patol, Barcelona, Spain

:
 Hosp Gen Univ Alicante, Inst Invest Sanitaria & Biomed Alicante ISABIAL, Dept Patol, Alicante, Spain

Garcia-Caballero, T:
 Univ Santiago, Fac Med & Odontol, Dept CienciasMorfol, Santiago De Compostela, Spain

Lopez, A:
 Complejo Hosp Univ A Coruna, Serv Anat Patol, Biobanco INIBIC, La Coruna, Spain

Suarez-Gauthier, A:
 Hosp Univ HM Sanchinarro, Dept Anat Patol, Lab Dianas Terapeut, Madrid, Spain

Ruiz, I:
 Hosp Univ Donostia, Serv Patol, Donostia San Sebastian, Spain

Rojo, F:
 Fdn Jimenez Diaz, CIBERONC, IIS, Serv Anat Patol, Madrid, Spain
ISSN: 17448301





Future Oncology
Editorial
Future Medicine Ltd., UNITEC HOUSE, 3RD FLOOR, 2 ALBERT PLACE, FINCHLEY CENTRAL, LONDON, N3 1QB, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 17 Número: 10
Páginas: 1209-1218
WOS Id: 000596532600001
ID de PubMed: 33289433
imagen Green Published, Hybrid Gold

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