Ongoing prostate cancer clinical trial shows an increased risk of death and fractures
The European Medicines Agency (EMA) announced upon the meeting of its Pharmacovigilance Risk Assessment Committee (PRAC) held on 27 to 30 November 2017 that itis investigating an increased risk of death and fractures reported in an ongoing clinical trial with the prostate cancer medicine radium-223 dichloride (Xofigo).
The clinical trial is comparing Xofigo with placebo, both given in combination with
abiraterone acetate (Zytiga) and prednisone/prednisolone. It includes prostate cancer patients with no symptoms or only mild symptoms, such as pain.
A preliminary analysis by an independent committee responsible for overseeing the trial reported a rate of death of 27% (109 out of 401 patients) for the Xofigo combination compared with 20% (82 out of 405 patients) for the placebo combination. Fractures also occurred more frequently with the Xofigo combination than the placebo combination (24% versus 7%).
Patients in this study are no longer treated with Xofigo and all the patients involved are being monitored closely.
The EMA’s PRAC will review the full results of this study as well as other available data to evaluate their impact on the authorised use of Xofigo.
While a full investigation is ongoing, doctors are asked not to use Xofigo in combination with Zytiga and prednisone/prednisolone to treat metastatic castration-resistant prostate cancer (mCRPC) patients.
Patients who are currently being treated with Xofigo and have any questions about their treatment should contact their doctor.
Xofigo is used to treat adult men with cancer of the prostate. It is authorised for use when medical or surgical castration does not work, and when the cancer has spread to the bones and is causing symptoms such as pain. Zytiga is used in men with mCRPC.
The ongoing study of Xofigo in combination with Zytiga and prednisone/prednisolone included patients with CRPC that has spread mainly to the bones, who have no symptoms or only mild symptoms and who have not been treated with chemotherapy.
Xofigo was authorised in the European Union in November 2013.
The review of Xofigo has been initiated at the request of the European Commission, under
Article 20 of Regulation (EC) No 726/2004. The review is being carried out by the PRAC, the Committee responsible for the evaluation of safety issues for human medicines, which will make a set of recommendations. The PRAC recommendations will then be forwarded to the Committee for Medicinal Products for Human Use CHMP, responsible for questions concerning medicines for human use, which will adopt an opinion. The final stage of the review procedure is the adoption by the European Commission of a legally binding decision applicable in all EU Member States.