The objective of this retrospective study is to examine the outcome of patients who relapse with Ph+ ALL and to potentially identify response profiles in order toadvance the treatment regimens that can be offered.
Study Type
OBSERVATIONAL
Enrollment
500
GRAALL
Pierre-Bénite, France
RECRUITINGLong term survival
Time frame: 5 years
10 year-survival
Time frame: 10 years
Molecular response (BCR::ABL1 ratio)
Molecular response is assessed using BCR::ABL1 ratio, on bone marrow if available (if not, on blood)
Time frame: At the end of each line of treatment, at each relapse, at 5 years after the last relapse, at 10 years after the last relapse
Hematologic response
Hematologic response is defined by less than 5% of blasts on bone marrow aspiration
Time frame: At the end of each line of treatment, at each relapse, at 5 years after the last relapse, at 10 years after the last relapse
Death date
Time frame: Up to 10 years
Cause of death
Cause of death can be : 1)disease, 2)complications related to treatment except bone marrow transplant, 3)Hematopoietic Stem Cells Transplantation related, 4)other
Time frame: Up to 10 years
Treatment characteristics (treatment name)
Name of chemotherapy or immunotherapy used
Time frame: At day 1 of each new treatment of relapse
Treatment characteristics (treatment dates)
Start date and end date of treatment
Time frame: At day 1 and at the end of each line of treatment of relapse
Treatment characteristics (dose)
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Dose of each treatment
Time frame: At day 1 of each new treatment of relapse