Since 13 November 2013, XOFIGO has been authorised on the European zone for the treatment of patients with prostate cancer, in the phase of resistance to castration, with symptomatic bone metastases. bone metastases frequently give rise to "bone events" that include spinal cord compressions and pathological fractures requiring surgery or external radiotherapy. Bone metastases are an important cause of death, disability, quality of life degradation and increase the cost of treatment. Xofigo is indicated in patients with bone metastases symptomatic of hormone-resistant prostate cancer and without known visceral metastases.
Since 13 November 2013, XOFIGO has been authorised on the European zone for the treatment of patients with prostate cancer, in the phase of resistance to castration, with symptomatic bone metastases. Prostate cancer is the most common non-cutaneous cancer in men internationally, and more than 90% of patients with hormone-resistant prostate cancer will have bone metastases. They frequently give rise to "bone events" that include spinal cord compressions and pathological fractures requiring surgery or external radiotherapy. Bone metastases are an important cause of death, disability, quality of life degradation and increase the cost of treatment. There is therefore a need for bone-targeting therapeutic agents that provide a benefit in terms of survival. Xofigo is indicated in patients with bone metastases symptomatic of hormone-resistant prostate cancer and without known visceral metastases. This treatment appears to have fewer side effects than chemotherapy (and does not call into question subsequent chemotherapy) or that the currently available metabolic bone radiotherapy as well as better pain control and survival gain than the latter do not
Study Type
OBSERVATIONAL
Enrollment
67
The various clinicam database will be collected solely to meet the objectives of the study. All data collected to create the database for this project will be anonymized
Icm Val D'Aurelle
Montpellier, Herault, France
ICO Bordeaux
Bordeaux, France
UP Clermont Ferrand
Clermont-Ferrand, France
Chu Grenoble
Grenoble, France
IPC Marseille
Marseille, France
CRLC de Nantes
Nantes, France
APHP Hopital Cochin
Paris, France
ONCOLOPE
Toulouse, France
Assess the epidemiological characteristics of the treated patient population
clinical data collection in the medical record
Time frame: during the treatment of XOFIGO an average of 24 weeks
Assess the presence of adverse events resulting from short-term and medium-term XOFIGO treatment
clinical data collection in the medical record
Time frame: during the treatment of XOFIGO an average of 24 weeks
Assess the number of patients who were able to benefit from the complete treatment (6 cycles)
clinical data collection in the medical record
Time frame: during the treatment of XOFIGO an average of 24 weeks
Collect the causes of premature discontinuation of treatment
clinical data collection in the medical record
Time frame: during the treatment of XOFIGO an average of 24 weeks
assess the antalgic effet of treatment (number of antalgic taken and how many time)
clinical data collection in the medical record
Time frame: during the treatment of XOFIGO an average of 24 weeks
assess the overall survival
clinical data collection in the medical record
Time frame: during the treatment of XOFIGO an average of 24 weeks
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