Lenvatinib
Cross-source consensus on Lenvatinib from 1 sources and 3 claims.
1 sources · 3 claims
How it works
Dosage & preparation
Evidence quality
Highlighted claims
- In NEO-ERA-01, lenvatinib is administered at 8 mg daily, started on Day 5 of each neoadjuvant cycle. — Neoadjuvant hepatic arterial infusion chemotherapy (HAIC) with GEMOX and lenvatinib in combination with adebrelimab for resectable high-risk recurrent intrahepatic cholangiocarcinoma (ICC): study protocol of the NEO-ERA-01 feasibility trial
- Lenvatinib contributes anti-angiogenic activity and may modulate the tumor immune microenvironment. — Neoadjuvant hepatic arterial infusion chemotherapy (HAIC) with GEMOX and lenvatinib in combination with adebrelimab for resectable high-risk recurrent intrahepatic cholangiocarcinoma (ICC): study protocol of the NEO-ERA-01 feasibility trial
- Preclinical synergy and phase II data support combining lenvatinib with chemotherapy and PD-L1 inhibition before surgery. — Neoadjuvant hepatic arterial infusion chemotherapy (HAIC) with GEMOX and lenvatinib in combination with adebrelimab for resectable high-risk recurrent intrahepatic cholangiocarcinoma (ICC): study protocol of the NEO-ERA-01 feasibility trial