ALL Ph Positive Clinical Trial
Official title:
A Multicenter Total Therapy Strategy for De Novo Adult Philadelphia Chromosome Positive (Ph+) Acute Lymphoblastic Leukemia (ALL) Patients. GIMEMA Protocol LAL1509, EudraCT Number 2010-019119-39
This study will enroll adult de novo Ph+ acute lymphoblastic leukemia (ALL) patients (≥18 years, ≤60 years). Induction treatment will consist of 12 weeks of Dasatinib oral administration (140 mg QD). Patients will initiate treatment with steroids 7 days prior to starting Dasatinib and will continue up to day 31. Patients will continue treatment with Dasatinib up to day 84, except for disease progression, intolerable toxicity, or withdrawal from study.
This study will enroll adult de novo Ph+ acute lymphoblastic leukemia (ALL) patients (≥18
years, ≤60 years). Induction treatment will consist of 12 weeks of Dasatinib oral
administration (140 mg QD). Patients will initiate treatment with steroids 7 days prior to
starting Dasatinib and will continue up to day 31. Patients will continue treatment with
Dasatinib up to day 84, except for disease progression, intolerable toxicity, or withdrawal
from study.
Thereafter:
- patients in hematological and molecular CR will receive a post-remissional treatment
consisting of Dasatinib alone for a 6 months period
- patients in hematological CR with persistence of molecular disease will be allografted
or, if not eligible or a donor is not available, treated with 2 cycles of a
Clofarabine-Cyclophosphamide schedule.
After allograft:
- MRD negative patients (i.e. in CHR and PCR negative) will receive a 6 months Dasatinib
maintenance treatment;
- MRD positive patients (i.e. in CHR and PCR positive) will receive Dasatinib as
maintenance treatment until relapse or progression.
Patients not transplanted and treated with Clofarabine/Cyclophosphamide will also receive
Dasatinib as maintenance treatment until relapse or progression.
;