Site for S2206 Phase III Trial of Neoadjuvant Durvalumab (NSC 778709) plus Chemotherapy versus Chemotherapy Alone for Adults with MammaPrint Ultrahigh (MP2) Hormone Receptor (HR) Positive / Human Epidermal Growth Factor Receptor (HER2) Negative Stage II-III Breast Cancer
Are you eligible to participate in this study?
You may be eligible for this study if you meet the following criteria:
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Conditions: Mammaprint Ultrahigh (mp2) Hormone Receptor (hr) Positive / Human Epidermal Growth Factor Receptor (her2) Negative Stage Ii-iii Breast Cancer
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Age: Between 18 Year(s) - 100 Year(s)
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Gender: Male or Female
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Other Inclusion Criteria:
- Participants must have histologically confirmed ER positive and/or PR positive (hormone receptor positive) and HER2 negative breast cancer
- Participants must have clinical stage II or III breast cancer
- Participants must not have metastatic disease
You may not be eligible for this study if the following are true:
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- Participants have locally recurrent breast cancer
- Participants have received any prior treatment for their current breast cancer, including chemotherapy, immunotherapy, biologic or hormonal therapy, and must be candidates for doxorubicin, paclitaxel, and durvalumab therapy
- Participants have a history of (non-infectious) pneumonitis that required steroids or evidence of active pneumonitis
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.