| Literature DB >> 33300372 |
Matthew H Taylor1, Emmett V Schmidt2, Corina Dutcus3, Elaine M Pinheiro2, Yasuhiro Funahashi4, Gregory Lubiniecki2, Drew Rasco5.
Abstract
Tumor progression and immune evasion result from multiple oncogenic and immunosuppressive signals within the tumor microenvironment. The combined blockade of VEGF and inhibitory immune checkpoint signaling has been shown to enhance immune activation and tumor destruction in preclinical models. The LEAP clinical trial program is evaluating the safety and efficacy of lenvatinib (a multikinase inhibitor) plus pembrolizumab (a PD-1 inhibitor) across several solid tumor types. Preliminary results from ongoing trials demonstrate robust antitumor activity and durable responses across diverse tumor types with a manageable safety profile. Thus, lenvatinib plus pembrolizumab is anticipated to be an important potential new regimen for several solid cancers that currently have limited therapeutic options. Clinical trial registration: NCT03884101, NCT03713593, NCT03820986, NCT03776136, NCT03797326, NCT03829319, NCT03829332, NCT03976375, NCT04428151, NCT04199104, NCT03898180, NCT04246177 (ClinicalTrials.gov).Entities:
Keywords: LEAP program; combination therapy; lenvatinib; pembrolizumab; solid tumors
Year: 2020 PMID: 33300372 DOI: 10.2217/fon-2020-0937
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404