Dr. Khan on Implications of the REFLECT Trial in HCC

Gazala N. Khan, MD
Published: Wednesday, May 22, 2019



Gazala N. Khan, MD, medical oncologist, Henry Ford Health System, discusses the implications of the REFLECT trial in advanced hepatocellular carcinoma (HCC).

The REFLECT trial was a large, randomized, phase III, noninferiority trial looking at lenvatinib (Lenvima) versus sorafenib (Nexavar) in the frontline setting of advanced HCC. The study was positive in that lenvatinib met all of its noninferiority endpoints compared with the standard of care, sorafenib. Specifically, lenvatinib demonstrated a median overall survival (OS) of 13.6 months versus 12.3 months with sorafenib (HR, 0.92; 95% CI, 0.79-1.06).

Based on these data, Khan says lenvatinib is as effective as sorafenib on all fronts. In addition to overall survival, investigators looked at progression-free survival (PFS) and time to progression as secondary endpoints. Similarly, lenvatinib appeared to be superior in PFS, time to progression, as well as response rate, says Khan. As such, the FDA approved the agent in August 2018 for use as frontline therapy in patients with unresectable HCC.
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Gazala N. Khan, MD, medical oncologist, Henry Ford Health System, discusses the implications of the REFLECT trial in advanced hepatocellular carcinoma (HCC).

The REFLECT trial was a large, randomized, phase III, noninferiority trial looking at lenvatinib (Lenvima) versus sorafenib (Nexavar) in the frontline setting of advanced HCC. The study was positive in that lenvatinib met all of its noninferiority endpoints compared with the standard of care, sorafenib. Specifically, lenvatinib demonstrated a median overall survival (OS) of 13.6 months versus 12.3 months with sorafenib (HR, 0.92; 95% CI, 0.79-1.06).

Based on these data, Khan says lenvatinib is as effective as sorafenib on all fronts. In addition to overall survival, investigators looked at progression-free survival (PFS) and time to progression as secondary endpoints. Similarly, lenvatinib appeared to be superior in PFS, time to progression, as well as response rate, says Khan. As such, the FDA approved the agent in August 2018 for use as frontline therapy in patients with unresectable HCC.

View Conference Coverage
Online CME Activities
TitleExpiration DateCME Credits
Oncology Briefings™: Individualizing Treatment After Second-Line Therapy for Patients With mCRCAug 29, 20191.0
Community Practice Connections™: Navigating New Sequencing Challenges for the Treatment of Hepatocellular CarcinomaAug 30, 20191.5
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