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Association details:
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Azacitidine and Entinostat in Treating Patients With Advanced Breast Cancer

Excerpt:
...- Patients with triple negative disease must have progressed through at least 1 prior chemotherapy regimen (administered in the adjuvant or metastatic setting); hormone receptor-positive patients must have progressed through two lines of hormonal therapy (administered in the adjuvant or metastatic setting), unless otherwise eligible as per below, and at least 1 prior chemotherapy regimen (administered in the adjuvant or metastatic setting) with...
Trial ID:
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Phase 1 trial of entinostat as monotherapy and combined with exemestane in Japanese patients with hormone receptor-positive advanced breast cancer

Published date:
11/24/2021
Excerpt:
This phase 1 study (3 + 3 dose-escalation design) enrolled postmenopausal women with advanced/metastatic HR+ BC...Six patients (50%) achieved stable disease (SD) for ≥ 6 months, including one treated for > 19 months. Median progression-free survival was 13.9 months (95% CI 1.9-not calculable); median overall survival was not reached....Entinostat monotherapy and combined entinostat/exemestane were well tolerated in Japanese patients...
Secondary therapy:
exemestane
DOI:
10.1186/s12885-021-08973-4
Trial ID:
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Phase 1 trial of entinostat as monotherapy and combined with exemestane in Japanese patients with hormone receptor-positive advanced breast cancer

Published date:
11/24/2021
Excerpt:
This phase 1 study (3 + 3 dose-escalation design) enrolled postmenopausal women with advanced/metastatic HR+ BC...Six patients (50%) achieved stable disease (SD) for ≥ 6 months, including one treated for > 19 months. Median progression-free survival was 13.9 months (95% CI 1.9-not calculable); median overall survival was not reached....Entinostat monotherapy and combined entinostat/exemestane were well tolerated in Japanese patients...
DOI:
10.1186/s12885-021-08973-4
Trial ID: