ResOs

National network specialized in pathology and care of bone sarcomas

SarcomaBCB

L’ANSM suspend les essais masitinib promus par AB Science. Le GSF-GETO recommande imatinib ou sunitinib en remplacement.

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Data dictionary


Birth date
ID : 140
Type : Free value
Content : DATE
Mandatory : Yes
Multiple values : No
Unique : No
Description : The patient's birth date

Sex
ID : 141
Type : Constrained
Content : TEXT
Mandatory : Yes
Multiple values : No
Unique : No
Description : The patient's gender
Possible values :
Female, Male

Patient information
ID : 1032
Type : Constrained
Content : TEXT
Mandatory : No
Multiple values : No
Unique : No
Description : Consent information
Possible values :
Uninformed, Addressed mail, No opposition, Opposition, Consent

Initials
ID : 1031
Type : Free value
Content : TEXT
Mandatory : Yes
Multiple values : No
Unique : No
Description : Patient initials : 4 characters (2 of Lastname, 2 of Firstname)Attention to compound names

Centre (RESOS)
ID : 1072
Type : Constrained
Content : TEXT
Mandatory : Yes
Multiple values : No
Unique : No
Description : Centre RESOS
Possible values :
Lyon CLB, CHU Rouen, IUCT Toulouse, Hôp. Pontchaillou, Bicêtre, Bergonié, Curie, CHRU Caen, Strasbourg CHU, Timone, Cochin, Tours Trousseau, Nantes CHU, CHU Nancy, Rangueil Toulouse, CHRU Lille, Bordeaux Pellegrin

Significant previous history
ID : 1
Type : Constrained
Content : TEXT
Mandatory : No
Multiple values : Yes
Unique : No
Description : No: no significant previous historyNF1: presence of neurofibromatosis type 1 or Recklinghausen diseaseNF2: presence of neurofibromatosis type 2Radiation therapy: tumour developed in a previously radiated areaLymphoedema: tumour developed on a preexisting lymphoedemaGardner: presence of a Gardner syndromLi Fraumeni: presence of a Li Fraumeni diseasePrevious cancer: the patient has previously developed another cancer different from the current tumourOther: other significant previous history with a possible link with the current tumour
Possible values :
No, Previous cancer, NF1, Gardner syndrome, Li Fraumeni syndrome, Retinoblastoma syndrome, Ollier disease, Maffucci syndrome, Paget disease, Multiple osteochondromas, McCune-Albright syndrome, Rothmund-Thomson syndrome, Werner syndrome, Cherubism, Other genetic disease, Other, Unknown

Creation date patient
ID : 181
Type : Free value
Content : DATE
Mandatory : Yes
Multiple values : No
Unique : No
Description : The date when the patient has been created in the database