NRG-BR009 OFSET (Breast Cancer) - Clinical Trial

¿Cuál es el Propósito de este estudio?

We are doing this study to compare two commonly used treatment choices for early-stage breast cancer in premenopausal women. We want to know if either option is a better choice than the other.

¿Cuál es la Condición que se está estudiando?

ER-Positive & HER2-Negative Breast Cancer

¿Quién puede participar en el Estudio?

Adults ages 18+ who:

  • Are diagnosed with breast cancer that is ER-positive and HER2-negative
  • Are premenopausal (have evidence of functioning ovaries)

For more information about who can join this study, contact the study team at nick.jeffries@duke.edu.

Grupo etario
Adultos

¿Qué Implica?

If you choose to join this study, you will be get a random assignment (like a coin flip) to 1 of 2 groups:

Group 1: If you are in this group, you will get the usual hormonal drugs to treat this type of cancer. You will get a drug as a pill you take by mouth every day. You will continue to receive the hormonal drug daily for at least 5 years unless you develop an allergy or severe side effects to the drug, or your breast cancer returns. You will get an injection of an ovarian suppression drug.

Group 2: If you are in this group, you will get the usual chemotherapy chosen by your doctor to treat this type of cancer. You also will get the usual hormonal drugs to treat this type of cancer. You will get a hormonal drug as a pill you take by mouth every day. You will continue to receive the hormonal drug daily for at least 5 years unless you develop an allergy or severe side effects to the drug, or your breast cancer returns. You will get an injection of an ovarian suppression drug.

Detalles del Estudio

Título Completo
NRG-BR009: A Phase III Adjuvant Trial Evaluating the Addition of Adjuvant Chemotherapy to Ovarian Function Suppression Plus Endocrine Therapy in Premenopausal Patients with pN0-1, ER-Positive/HER2-Negative Breast Cancer and an Oncotype Recurrence Score
Investigador Principal
Alexandra Thomas, MD, FACP
Especialista en oncología médica
Número de Protocolo
IRB: PRO00115431
NCT: NCT05879926
Fase
Phase III
ClinicalTrials.gov
Estado de inscripción
Abierto para inscripción
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Contribuya a Duke Health