Increasing Liver Cancer Treatment Options

The FDA has approved expanding the use of lenvatinib to treat certain patients with the most common type of liver cancer.

The U.S. Food and Drug Administration (FDA) recently approved expanding the use of the molecularly targeted therapeutic lenvatinib (Lenvima) to include treating certain patients with the most common type of liver cancer, hepatocellular carcinoma.

Under the expanded approval, lenvatinib can be used as an initial treatment for patients who have hepatocellular carcinoma that cannot be treated with surgery.

Liver cancer is the third type of cancer that the FDA has approved lenvatinib for treating. It was approved for certain patients with thyroid cancer and kidney cancer in Feb. 2015 and May 2016, respectively.

Liver cancer incidence has been increasing in the United States for the past four decades, according to data from the National Cancer Institute. New approaches to treatment are urgently needed because the five-year relative survival rate has improved little during that time; it remains at just 17.7 percent.

Most of the 42,220 new cases of liver cancer expected to be diagnosed in the United States in 2018 will be classed as hepatocellular carcinoma. Many patients diagnosed with advanced hepatocellular carcinoma are treated with sorafenib (Nexavar).

The approval of lenvatinib as an initial treatment for patients who have hepatocellular carcinoma that cannot be treated with surgery was based on results from the phase III REFLECT clinical trial. The results, which were published in the Lancet, showed that lenvatinib was not inferior to sorafenib in overall survival, nor was it statistically significantly better; median overall survival was 13.6 months among the 478 patients who received lenvatinib compared with 12.3 months among the 476 patients who received sorafenib.

Sorafenib and lenvatinib exert their anticancer effects in similar ways. They both target multiple proteins called tyrosine kinases, which promote growth and cancer progression in different ways. Some of the tyrosine kinases sorafenib and lenvatinib target promote the growth of the blood and lymphatic vessel networks that tumors establish to grow and survive. Thus, one effect of these molecularly targeted therapeutics is to impede the growth of new blood and lymphatic vessels. As such, they are known as antiangiogenic therapeutics, as well as molecularly targeted therapeutics.

This article was adapted with permission from a post on the AACR's official blog, CANCER RESEARCH Catalyst. The FDA approval was rendered on Aug. 16, 2018. Find out more about the decision on the FDA website.

Last year the AACR provided over $49 million in grants and awards funding lifesaving cancer research. There are many ways you can support our mission to prevent and cure all cancers. Take Action

The American Association for Cancer Research (AACR) is a 501c3 registered nonprofit organization with offices at 615 Chestnut Street, 17th Floor, Philadelphia, PA 19106 | 215.440.9300