Age
Item
patients must have reached their 18th birthday
boolean
C0001779 (UMLS CUI [1])
Childbearing Potential Contraceptive methods
Item
women of childbearing potential must agree to use effective methods of contraception
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Social Security Program Affiliated
Item
patients must be affiliated to a social security regime
boolean
C0037435 (UMLS CUI [1,1])
C1510826 (UMLS CUI [1,2])
Imatinib
Item
patients must have received imatinib therapy for at least 36 months.
boolean
C0935989 (UMLS CUI [1])
Molecular Complete Response | RT-PCR Measures Negative Quantity | BCR-ABL Transcript
Item
patients must be in complete molecular remission during at least two consecutive years with at least five rt-pcr negative measures for bcr-abl transcripts.
boolean
C4050308 (UMLS CUI [1])
C0599161 (UMLS CUI [2,1])
C0079809 (UMLS CUI [2,2])
C1513916 (UMLS CUI [2,3])
C1265611 (UMLS CUI [2,4])
C1835417 (UMLS CUI [3,1])
C1519595 (UMLS CUI [3,2])
HIV negative | Hepatitis C test negative | Hepatitis B test negative
Item
patients must be hiv, hcv and hbv negatives
boolean
C0481430 (UMLS CUI [1])
C1619717 (UMLS CUI [2])
C1611173 (UMLS CUI [3])
Follow-up Molecular
Item
patients who have molecular follow-up realized in accordance with international recommendations
boolean
C1522577 (UMLS CUI [1,1])
C1521991 (UMLS CUI [1,2])
Informed Consent
Item
all patients must be informed of the investigational nature of this study and must sign and give written informed consent.
boolean
C0021430 (UMLS CUI [1])
Patients Protection Law | Informed Consent Unable
Item
patients who are protected by the law. patients who are unable to give their consent to participate to the study.
boolean
C0030705 (UMLS CUI [1,1])
C1545588 (UMLS CUI [1,2])
C0220866 (UMLS CUI [1,3])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Imatinib Discontinued | Pathology At risk for relapse | Therapeutic procedure At risk for relapse | Pathology Interferes with Study immunologic | Therapeutic procedure Interferes with Study immunologic | Exception Interferon
Item
patients who have pathologies or treatments that are able to enhance the potential relapse risk after stopping imatinib. patients who have pathologies or treatments which able to interfere with immunologic study (excepted ifn α):
boolean
C0935989 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C0677042 (UMLS CUI [2,1])
C1320679 (UMLS CUI [2,2])
C0087111 (UMLS CUI [3,1])
C1320679 (UMLS CUI [3,2])
C0677042 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C2603343 (UMLS CUI [4,3])
C0205470 (UMLS CUI [4,4])
C0087111 (UMLS CUI [5,1])
C0521102 (UMLS CUI [5,2])
C2603343 (UMLS CUI [5,3])
C0205470 (UMLS CUI [5,4])
C1705847 (UMLS CUI [6,1])
C3652465 (UMLS CUI [6,2])
Adrenal Cortex Hormones | Immunosuppressive Agents | Chemotherapy Malignant Neoplasms | Therapeutic radiology procedure Malignant Neoplasms | Hemopoietic stem cell transplantation | Hemopoietic stem cell transplantation Planned
Item
corticosteroids or other immuno suppressors other concomitant malign pathology treated by chemotherapy or radiotherapy previous or programmed haematopoietic stem cell allogreffe
boolean
C0001617 (UMLS CUI [1])
C0021081 (UMLS CUI [2])
C0392920 (UMLS CUI [3,1])
C0006826 (UMLS CUI [3,2])
C1522449 (UMLS CUI [4,1])
C0006826 (UMLS CUI [4,2])
C0472699 (UMLS CUI [5])
C0472699 (UMLS CUI [6,1])
C1301732 (UMLS CUI [6,2])