About this trial
An observatory for patients aged 18 years and over with Philadelphia chromosome positive (Ph+ or BCR::ABL1) acute lymphoblastic leukemia (ALL) and treated with the combination of BCR::ABL1 inhibitors and chemotherapy and/or corticosteroids and/or a monoclonal antibody.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Male or female patients ≥ 18 years
Philadelphia chromosome or BCR::ABL1 positive acute lymphoblastic leukaemia
Treatment with the combination of BCR::ABL1 inhibitors and chemotherapy and/or corticotherapy and/or a monoclonal antibody
Disqualifiers
Patients deceded and having previously refused data collection
Not included in a prospective clinical trial
Trial population
Acute Lmphoblastic Leukaemia with Philadelphia chromosome or BCR::ABL1 positive
Trial design
Cohort
Other
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Overall survival by 12 months
Secondary outcomes
overal survival by 36 months
proportion of complete remission
the molecular response defined by BCR//ABL1/ABL1 ratio in bone marrow and/or peripheral blood
the molecular response defined by IGTR quantification proportion in bone marrow and/or peripheral blood
Sponsors and contacts
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