The aim of this study is to establish a common geriatric oncology medical database. The patients concerned are the patients having benefited from a geriatric oncology consultation in one of the participating centres. This database is designed with a view on the one hand to better describe to better understand this population and on the other hand to facilitate the conduct of future retrospective or prospective studies on this population. The constitution of this observatory of patients seen in consultation should facilitate the development of studies from the analysis of data collected, and occasional surveys by the rapid identification of cases. Data from this database could provide clinicians with valuable informative elements of descriptive epidemiology and concerning the organization of care in the geriatric oncology field.
The study is presented during the first consultation of oncogeriatric care or after this consultation (for patients having benefited from the consultation between January 2014 and October 2014) : the patient is informed with an information note and is told that he can express its opposition to the use of its clinical data. In case of no opposition from the patient, the referent geriatrician will complete the patient form with the requested data and will forward it for computerized processing.
Study Type
OBSERVATIONAL
Enrollment
2,914
Centre Hospitalier d'Arras
Arras, France
Centre Hospitalier
Béthune, France
Centre Hospitalier
Boulogne-sur-Mer, France
Centre Hospitalier, Douai
Douai, France
Centre Hospitalier
Dunkirk, France
Hospitalier Le Cateau-Cambresis
Le Cateau-Cambrésis, France
Polyclinique de Riaumont
Liévin, France
CHRU de Lille
Lille, France
Hôpital Saint Vincent de Paul
Lille, France
Centre Oscar Lambret
Lille, France
...and 5 more locations
Measurement of the prevalence of different clinical criteria of interest : demographic characteristics, disease state, patient status according to the geriatric criteria (Comprehensive Geriatric Assessment (CGA)).
Time frame: Up to 5 years
Measurement of the prevalence of different medical and social criteria of interest.
Patient's life characteristics (place of living, isolation) and the helps set up (presence of a natural caregiver, sources of professional help).
Time frame: Up to 5 years
Measurement of the association between one or more factors of interest (clinical, biological and medical and social) related to a proposal to amend or not the initially proposed therapeutic strategy.
Time frame: Up to 5 years
Percentage of patients included in trials.
Time frame: Up to 5 years
Temporal evolutions of clinical, medical and social characteristics.
Time frame: Up to 5 years
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