A multicenter, phase Ib/II, open-label study of tivozanib with durvalumab in advanced hepatocellular carcinoma (DEDUCTIVE)

Author:

Mahmood Sharmeen1,Li Daneng2,Lee Arielle3,Rowe Julie4,Beg Muhammed5,Kasturi Vijay6,Iyer Renuka7,Abrams Thomas8,Dayyani Farshid1ORCID

Affiliation:

1. UC Irvine Health, Orange, CA 92868, USA

2. City of Hope Comprehensive Cancer Center, Duarte, CA 91010, USA

3. University of Texas Health East Texas HOPE Cancer Center, Tyler, TX 75708, USA

4. University of Texas School of Health Sciences at Houston, Houston, TX 77030, USA

5. University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

6. AVEO Oncology, Boston, MA 02108, USA

7. Roswell Park Comprehensive Cancer Center, Buffalo, NY 14203, USA

8. Dana Farber Cancer Institute, Boston, MA 02215, USA

Abstract

Durvalumab, a PD-L1 inhibitor, is part of an immunotherapeutic drug class shown to have prolonged survival benefit in patients with advanced stage hepatocellular carcinoma (HCC). Tivozanib is a potent and selective VEGFR 1, 2 and 3 tyrosine kinase inhibitor. While these medications have both demonstrated single-agent activity in HCC and have been combined safely with other therapies, there is no data on their concurrent therapeutic effects. In the phase Ib DEDUCTIVE trial, the combination of tivozanib plus durvalumab is evaluated for safety and tolerability. Here, the design of and rationale for this trial in both treatment naive patients and those who progress on atezolizumab and bevacizumab for advanced or metastatic HCC are described. Clinical Trial Registration: NCT03970616

Funder

AVEO Oncology

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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