Abemaciclib Combined With FOLFOX/FOLFIRI Regimen in Patients With Advanced Colorectal Liver Metastases Cancer
- Sponsor
- Fudan University
- Study ID
- NCT07441369
- Phase
- PHASE2
- Status
- Enrolling By Invitation
Conditions
- Liver Metastases From Colorectal Cancer (mCRC)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Abemaciclib — DRUGAbemaciclib was administered orally at 100-200mg twice daily for each 28-day cycle.
- Oxaliplatin — DRUG85mg/m², ivdrip, D1
- Calcium Folinate — DRUG400mg/m², ivdrip, D1; or calcium levofolinate, 200 mg/m², ivdrip, D1
- 5-Fluorouracil — DRUG400mg/m², iv, D1; and 2400mg/m², civ, 46-48h
- Irinotecan — DRUG180mg/m², ivdrip, D1
Study Details
This is a single-center, single-arm, open-label clinical study, to explore the efficacy and safety of abemaciclib combined with FOLFOX/FOLFIRI regimen in patients with advanced colorectal liver metastases cancer who failed standard two or three-line therapy.
Key Dates
- Start date
- May 1, 2026
- Status verified
- Apr 2026
- Primary completion
- Apr 30, 2027
- Completion
- Apr 30, 2027
Study Design
- Enrollment
- 16 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Abemaciclib+ mFOLFOX/FOLFIRIAbemaciclib was administered orally at 100-200mg twice daily for each 28-day cycle. mFOLFOX6 and FOLFIRI will be administered every 2-4 weeks.
Primary Outcome Measure
ORR [ Time Frame: 12 months ]