NICE recommends use of TheraSphere for treatment of primary and secondary liver cancer
BTG plc, the specialist healthcare company, announced that the National Institute for Health and Care Excellence (NICE) has issued guidance recommending the use of Selective Internal Radiation Therapy (SIRT), which includes TheraSphere, for patients with liver cancer across the NHS. The guidance supports the use of this innovative treatment for patients with primary hepatocellular carcinoma as well as for those with intrahepatic cholangiocarcinoma and follows the previous recommendation for its use in patients with colorectal cancer liver metastases.
The NHS in England is currently preparing guidelines on how SIRT should be used as a treatment option for patients with liver cancer, including those with colorectal cancer liver metastases and cholangiocarcinoma, after recently issuing an interim policy on how this therapy should be funded. It is anticipated that this latest NICE guidance will result in a similar evaluation for patients with primary liver cancer.
“NICE’s guidance further highlights the growing acceptance and understanding of radioembolization in the treatment of liver cancer,” said Peter Pattison, general manager TheraSphere. “With over 4,000 new liver cancer cases diagnosed annually in the UK5, this new guidance will potentially provide patients with access to a broader range of treatment options.”
Pattison added, “With many countries looking to the UK for direction on their own reimbursement decisions and processes, this guidance should lead to greater awareness amongst physicians and patients and may also prompt similar guidance in other geographies. In addition to increasing liver cancer treatment options for physicians and patients in the UK, this guidance will assist BTG as we continue to explore other reimbursement opportunities in various regions across the world.”
TheraSphere is a form of radioembolization therapy that consists of millions of small glass beads (20 to 30 micrometers in diameter) containing radioactive yttrium-90 (Y-90). The product is injected by physicians into the artery of the patient’s liver through a catheter, which allows for a high dose of radiation to be delivered directly to the tumour via blood flow thereby limiting the damage to surrounding healthy tissue and side effects to the patients.
TheraSphere is used in the European Union and in Canada for the treatment of hepatic neoplasia in patients who have appropriately positioned arterial catheters. Since its introduction in Europe, more than 1,000 patients have been treated with TheraSphere.
Common side effects include mild to moderate fatigue, pain and nausea for about a week. Physicians describe these symptoms as similar to those of the flu. Some patients experience some loss of appetite and temporary changes in several blood tests.
TheraSphere is manufactured by Nordion (Canada) Inc. for BTG International Canada Inc. TheraSphere is a trademark of Theragenics Corporation used under license by BTG International Canada Inc. BTG and the BTG roundel logo are trademarks of BTG International Ltd, and are registered trademarks in the US, EU and certain other territories. All rights reserved.
BTG is developing and commercialising products targeting critical care, cancer and varicose veins.