Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Anatomic Stage IV Breast Cancer AJCC v8
  • Hormone Receptor Positive Breast Carcinoma
  • Metastatic Breast Carcinoma
  • Prognostic Stage IV Breast Cancer AJCC v8
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 70 years and 125 years
Gender
Both males and females

Description

PRIMARY OBJECTIVE: I. To estimate the incidence of grade 3 or higher toxicities attributed to abemaciclib monotherapy in adults aged 70 or older with hormone receptor positive metastatic breast cancer. SECONDARY OBJECTIVES: I. To describe the full toxicity profile including all grade 2 and higher ad...

PRIMARY OBJECTIVE: I. To estimate the incidence of grade 3 or higher toxicities attributed to abemaciclib monotherapy in adults aged 70 or older with hormone receptor positive metastatic breast cancer. SECONDARY OBJECTIVES: I. To describe the full toxicity profile including all grade 2 and higher adverse events, and patient-reported adverse events (AEs) using Patients Reported Outcomes (PRO)-Common Terminology Criteria for Adverse Events (CTCAE) measures. II. To describe rates of dose reductions, dose holds, treatment discontinuations due to factors other than progression, and hospitalizations. III. To estimate median (and 95% confidence interval [CI]) failure-free survival, progression-free survival and overall survival. IV. To describe the results of Was It Worth It (WIWI) and Overall Treatment Utility (OTU) questionnaires. V. To describe the rate of adherence to abemaciclib. VI. To determine average plasma steady-state abemaciclib Ctrough concentrations. VII. To evaluate the association of adherence rate with abemaciclib plasma t-rough concentrations. VIII. To describe associations between cancer-specific, comprehensive Geriatric Assessment (cGA) scores and the incidence of toxicities and their grade. EXPLORATORY OBJECTIVE: I. To determine the association between biomarkers of aging and grades 3 or higher toxicity. OUTLINE: Patients receive abemaciclib orally (PO) twice daily (BID) on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up at 30 days, then every 6 months for 2 years.

Tracking Information

NCT #
NCT04305834
Collaborators
National Cancer Institute (NCI)
Investigators
Principal Investigator: Mina S Sedrak City of Hope Medical Center