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US FDA approval for cancer treatment Xofigo


Bayer HealthCare has announced that the US Food and Drug Administration (FDA) approved Xofigo® (radium 223 dichloride) for the treatment of patients with castration-resistant prostate cancer (CRPC), symptomatic bone metastases and no known visceral metastatic disease.
Xofigo is the first alpha particle-emitting radioactive therapeutic agent approved by the FDA that has demonstrated improvement in overall survival (OS) and delay in time to first symptomatic skeletal event (SSE) compared to placebo, as shown in the pivotal Phase III ALSYMPCA trial.
The commercial production of Xofigo is underway, and first doses are expected to be ready for patient treatment within a few weeks. Bayer has worldwide exclusive marketing rights for Xofigo. In the US, Bayer HealthCare and Algeta US, LLC will co-promote the product.
“Xofigo shows a favourable safety profile and has the potential to improve patient outcomes in a completely novel way. Radium 223 emits alpha particles that affect cancer cells in bone metastases and may contribute to a survival improvement,” said Kemal Malik, MD, member of the Bayer HealthCare Executive Committee and Head of Global Development. “This FDA approval will provide prostate cancer patients and the physicians who care for them with a new and innovative treatment option.” 
“Most men with advanced prostate cancer develop bone metastases, which can be life-threatening,” said Oliver Sartor, MD, North American Principal Investigator for the pivotal trial and medical director of the Tulane Cancer Center. “Xofigo has demonstrated an anti-tumour effect on bone metastases and an overall survival effect in prostate cancer, making it an important addition to the treatment of CRPC patients.”
Bone is the most common site in the body to be affected by metastatic cancer and bone metastases are particularly prevalent in patients with prostate cancer. Approximately 90% of patients with metastatic prostate cancer show evidence of bone metastases. Bone metastases can lead to an increase in frequency of skeletal events and have been shown to be the main cause of morbidity and death in patients with CRPC.
Efficacy and Safety Data Supporting Xofigo Approval
The approval of Xofigo (radium 223 dichloride, radium 223) is based on data from the pivotal Phase III ALSYMPCA (ALpharadin in SYMptomatic Prostate CAncer) trial. At the interim analysis, radium 223 significantly improved overall survival (OS) [HR=0.695 (95% CI 0.552-0.875), p=0.00185]; median OS was 14.0 months with radium 223 plus best standard of care versus 11.2 months with placebo plus best standard of care. Additionally, at the interim analysis there was a delay in the time to first symptomatic skeletal event (SSE) for patients treated with radium 223 versus placebo.
An updated analysis, conducted after the study was unblinded, showed a further improvement in overall survival (OS) for patients treated with radium 223 versus placebo, with a median OS of 14.9 months versus 11.3 months; HR=0.695 (95% CI 0.581-0.832).
The most common adverse reactions (greater than or equal to 10%) in patients receiving radium 223 in the ALSYMPCA trial were nausea, diarrhoea, vomiting and peripheral oedema. The most common haematologic laboratory abnormalities (greater than or equal to 10%) were anaemia, lymphocytopenia, leukopenia, thrombocytopenia and neutropenia.
About Xofigo® (radium 223 dichloride) Injection
Xofigo® with the active ingredient radium 223 dichloride (radium 223) is an alpha particle-emitting radioactive therapeutic agent with an anti-tumour effect on bone metastases. Radium 223 mimics calcium and forms complexes with the bone mineral hydroxyapatite at areas of increased bone turnover, such as bone metastases. The high linear energy transfer of alpha emitters may cause double-strand DNA breaks in adjacent cells, resulting in an anti-tumour effect on bone metastases. The alpha particle range from radium 223 is less than 100 micrometers, which may limit damage to the surrounding normal tissue.
Radium 223 is currently not approved by the European Medicines Agency (EMA) or other authorities outside the U.S. Bayer submitted a Marketing Authorisation Application to the EMA for radium 223 in December 2012 for the treatment of CRPC patients with bone metastases.
In September 2009, Bayer signed an agreement with Algeta ASA (Oslo, Norway) for the development and commercialisation of radium 223. Under the terms of the agreement, Bayer will develop, apply for health authority approvals worldwide and commercialise radium 223 globally. Algeta will co-promote radium 223 with Bayer in the U.S.
About the ALSYMPCA Trial
The ALSYMPCA trial was a Phase III, randomised, double-blind, placebo-controlled international study of radium 223 dichloride with best standard of care versus placebo with best standard of care in symptomatic CRPC patients with bone metastases. The trial enrolled 921 patients in more than 100 centres in 19 countries. The study treatment consisted of up to six intravenous injections of radium 223 or placebo each separated by an interval of four weeks.
The primary endpoint of the study was overall survival (OS). A key secondary endpoint was time to first symptomatic skeletal event (SSE), as defined as external beam radiation therapy (EBRT) to relieve skeletal symptoms, new symptomatic pathologic bone fracture, occurrence of spinal cord compression, or tumour-related orthopaedic surgical intervention.

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