Clinical trial

Prospective Study of Treatment Free Remission in Patients With Chronic Myeloid Leukemia in Chronic Phase Who Achieved Deep Molecular Response With Tyrosine Kinase Inhibitors in Real Life Setting in Argentina - (Argentine Stop Trial)

Name
Argentina Stop Trial
Description
The principal aim of this study is to evaluate complete molecular remission in patients with chronic myeloid leukemia (CML) in deep molecular response after stopping tyrosine kinase inhibitor (TKI) treatment. The second aim is to characterize the immunological status of patients with CML at the time of TKI interruption and then at 3 months after the interruption.
Trial arms
Trial start
2019-02-01
Estimated PCD
2022-06-01
Trial end
2025-01-01
Status
Recruiting
Treatment
Discontinuing treatment with Tyrosine Kinase Inhibitor after enrolment
Discontinuing treatment with Tyrosine Kinase Inhibitor after enrolment with a scheduled molecular monitoring until month 24.
Arms:
CML patient TKI discontinuation study
Size
75
Primary endpoint
Molecular relapse free survival during 24 months
24 months
Eligibility criteria
Inclusion criteria: 1. Signed Informed consent. 2. Patients with a diagnosis of CML BCR-ABL positive in CP treated with approved TKI (Imatinib, Nilotinib or Dasatinib) in 1st line or in 2nd line due to intolerance to the 1st line or in 2nd line due to the lack of deep MR with 1st line TKI, which never presented criteria for treatment failure. 3. Age ≥ 18 years 4. ≥ 4 years of treatment with imatinib, nilotinib or dasatinib. 5. Achievement of MR 4.5 in a standardized laboratory (BCR-ABL1 IS ≤ 0.0032%). 6. Evidence of MR 4.5 sustained for ≥ 2 years, as documented in at least 4 tests performed at least 3 months apart. 7. Evidence of typical quantifiable BCR-ABL1 transcript (b3a2 \[e14a2\] and / or b2a2 \[e13a2\], typical isoforms of p210). Exclusion criteria: 1. Patients who previously discontinued TKI and demonstrated recurrence of the disease. 2. Patients with failure to any TKI at any time. 3. Patients who presented accelerated phase or CML in blast crisis at any time. 4. Patients with atypical transcript not quantifiable by RT qPCR 5. BCR-ABL mutation detected at any time during the course of the resistant disease
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'interventionModelDescription': 'multicentre, open-label, uncontrolled trial', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 75, 'type': 'ESTIMATED'}}
Updated at
2023-07-03

1 organization

1 product

1 indication

Organization
Fundaleu