ALERTA PARA LOS PACIENTES: Las mascarillas son ahora opcionales en nuestras oficinas de la VOA. Si usted está inmunocomprometido o se siente enfermo, se recomienda encarecidamente el uso de mascarillas. Gracias. HAGA CLIC AQUÍ para más detalles.

Investigación clínica & Ensayos

USO 21537

Estudio aleatorizado, abierto, de fase 3 de Sacituzumab Govitecan frente al tratamiento de elección del médico en pacientes con cáncer de mama triple negativo localmente avanzado, inoperable o metastásico no tratado previamente y cuyos tumores no expresan PD-L1 o en pacientes previamente tratadas con agentes anti-PD-(L)1 en la fase inicial cuyos tumores sí expresan PD-L1 (GS-US-592-6238)

 

Tipos de enfermedades: Investigación sobre el cáncer de mama

Requisitos de elegibilidad:

Locally advanced (inoperable) or metastatic triple negative breast cancer that is PD-L1 negative with measurable disease, patients with PD-L1 positive tumors at screening may be eligible if they received treatment with PD-L1 inhibitor in neoadjuvant or adjuvant setting
-Must have completed treatment for stage I-III as indicated with 6 ≥ months between finishing treatment with curative intent and documented disease recurrence, de novo metastatic triple negative breast cancer allowed
-No: previous treatment for advanced disease; received systemic anticancer treatment within past 6 months or radiation treatment within last 2 weeks; received topoisomerase 1 inhibitors or antibody drug conjugatescontaining isomerase inhibitor; HIV positive patients with history of Kaposi’s sarcoma and/or multicentric Castleman’s disease; active Hep B or Hep C infection; have known active central nervous system metastasis or carcinomatous meningitis; allogenic tissue or solid organ transplant; myocardial infarction or unstable angina pectoris within last 6 months, history of ventricular arrhythmia or high grade atrioventricular block or other cardiac arrhythmias requiring antiarrhythmic medication, New York Heart Association Grade III or IV heart failure or ejection fraction < 40%, history of QT interval prolongation; have active chronic inflammatory bowel disease (ulcerative colitis or Crohn’s) or GI perforation in last 6 months

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