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Discontinuation study of nilotinib in patients with chronic myeloid leukemia who have maintained complete molecular remission for at least 2 years: the prospective, multicenter stop study in Japan adult leukemia study group

Discontinuation study of nilotinib in patients with chronic myeloid leukemia who have maintained complete molecular remission for at least 2 years: the prospective, multicenter stop study in Japan adult leukemia study group - JALSG-D-STOP216

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024985
Enrollment
50
Registered
2016-11-24
Start date
2016-11-24
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic myeloid leukemia

Interventions

Discontinuation of dasatinib and retreatment with dasatinib for CML patients who lost TFR

Sponsors

Japan Adult Leukemia Study Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. BCR-ABL-positive CML patients in chronic phase (CP) 2. CML patients in CP with ECOG Performance Status 0-2 3. CML patients in CP, who have been treated with dasatinib with a daily dose equal or more than 50mg for more than three years since diagnosis 4. CML patients in CP, who have maintained complete molecular response (CMR) for more than two years 5. CML patients in CP without severe (more than grade 3) adverse events by dasatinib 6. CML patients in CP, who agree to discontinuation of dasatinib 7. CML patients in CP, who can visit the hospital on scheduled days 8. CML patients in CP with written consent for the trial

Exclusion criteria

Exclusion criteria: 1. CML patients in CP, who had an experience of treatment with TKI other than dasatinib or interferon-a for more than 4 weeks 2. CML patients in CP, who have been treated with dasatinib with a daily dose less than 50mg excepting transient dose reduction due to the adverse events 3. CML patients in CP, who had an experience of allogeneic hematopoietic stem cell transplantation 4. CML patients in CP with an episode of disease progression to accelerated or blastic phase 5. CML patients in CP with an episode of loss of CMR despite the continuous treatment with dasatinib 6. CML patients in CP with poor adherence to dasatinib 7.CML patients in CP, who don't accept retreatment with dasatinib after losing TFR 8. CML patients in CP with other inappropriate conditions for the trial

Design outcomes

Primary

MeasureTime frame
TFR rate at 12 months after dasatinib discontinuation

Secondary

MeasureTime frame
1. TFR rate at 24 months after dasatinib discontinuation 2. CMR rate at 12 months and 24 months after dasatinib discontinuation 3. Overall survival, progression-free survival, treatment-free survival, event-free survival 4. Relationship between TFR and CMR duration time, treatment duration time, early molecular response, Sokal risk stratification, and trough concentration 5. Efficacy of the restartment with dasatinib for CML patients, who lost TFR 6. Analysis of clinical features of dasatinib withdrawal syndrome

Countries

Japan

Contacts

Public ContactItaru Matsumura

Kinki University, Faculty of Medicine Department of Hematology and Rheumatology

i.matsu@med.kindai.ac.jp072-366-0221

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026