Phase 1b Study of Olaparib and Estradiol in Advanced ER+ Breast Cancer (PHOEBE)
Summary
Determine the safety and recommended Phase II dose of olaparib in combination with 17b-estradiol in post-menopausal patients with advanced ER+/HER2- breast cancer.
Detailed description
Patients with endocrine-resistant ER+/HER2- breast cancer are eligible. Patients will be treated with the combination of 17b-estradiol and olaparib for 2 cycles, and then treated with single-agent 17b-estradiol until disease progression. Clinical benefit, progression-free survival, objective response, tumor metabolic response, and toxicity will be determined.
Arms & interventions
- DrugOlaparib
Participants will be treated with olaparib at the approved doses for the treatment of subtypes of breast cancer or at reduced dose/frequency for participants with moderate renal impairment.
- Drug17b-estradiol
17b-estradiol will be taken orally three times per day.
Outcome measures
Primary
Determine the Phase II dose of olaparib in combination with 17b-estradiol
Determine the safety and recommended Phase II dose of olaparib in combination with 17b-estradiol in post-menopausal patients with advanced ER+/HER2- breast cancer.
Time frame: 8 weeks
Secondary
Clinical benefit rate
Time frame: 6 months
Objective response rate
Time frame: 6 months
Progression-free survival
Time frame: 12 months
Plasma Olaparib concentration
Time frame: 6 hours
Plasma 17b-Estradiol/Estrone concentration
Time frame: 6 hours
Eligibility criteria
Study locations (1)
Dartmouth Cancer Center
Lebanon, New Hampshire, 03756