Study | study type
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Pathology | T1 | T0 | Patients | sample sizes | ROB | Results | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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la/mBC - HR positive breast cancer - HR positive la/mBC - HR positive | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
versus eribulin | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
pembrolizumab alone | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
NCT03051659, 2020 NCT03051659 | RCT | la/mBC - HR positive | eribulin mesylate plus pembrolizumab | eribulin mesylate monotherapy | Patients must have histologically or cytologically confirmed Stage IV invasive breast cancer, must have HR positive, HER2-negative breast cancer (ER>1% and/or, PR>1%, HER2-negative, must have already received or been intolerant to at least two lines of hormonal therapies (including the adjuvant or metastatic setting) or be appropriate candidates for chemotherapy, | 44 / 44 | NA | inconclusive |
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