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Persistence of MR3 in Chronic Myeloid Leukemia (CML) After a 2nd Stop of TKI Treatment (DASTOP2)

A

Amsterdam UMC, location VUmc

Status and phase

Unknown
Phase 2

Conditions

CML, Relapsed

Treatments

Drug: Dasatinib

Study type

Interventional

Funder types

Other

Identifiers

NCT03573596
DASTOP2

Details and patient eligibility

About

This study will enroll CML patients who have failed a first TKI stopping attempt. After failure and at least a year of TKI treatment, patients will proceed to dasatinib treatment for another 2 years. If MR4 or better is re-achieved and maintained for at least one year, patients will be eligible for a second stop. After verification of MR4, TKI treatment will be stopped and patients followed in the same manner as after first stop. If MMR is lost (BCR-ABL >0.1% (IS)), TKI treatment will once again be restarted.

Full description

The DASTOP2 study aims to retreat patients who relapse in the Euro-SKI study (or who stopped TKI treatment outside trials but according to EURO-SKI procedures), with TKI for at least another 3 years, out of last two years with dasatinib. If MR4 or better is re-achieved and maintained for at least one year, patients will be eligible for a second stop. After verification of MR4, TKI treatment will be stopped and patients followed in the same manner as after first stop. If MMR is lost (BCR-ABL >0.1% (IS)), TKI treatment will once again be restarted.

Patients exhibiting hematological relapse after first stop attempt will not be offered a second stop within this study. The same applies to patients in whom TKI was restarted prematurely (without loss of MMR).

Enrollment

134 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. CML in chronical phase (CP) under TKI treatment after failing a prior attempt to stop treatment within EURO-SKI or outside the study but according to EURO-SKI trial procedures. For the latter group this requires at least 3 years of TKI treatment (first line or second line due to intolerance to first line) before first stop, and MR4 for at least one year before stopping.
  2. Treated with TKI for at least one year after having failed a prior attempt to stop TKI. Previous TKI can be any.
  3. Typical BCR/ABL1 transcript (b3a2 and/or b2a2) must have been confirmed at diagnosis or later during the disease course.
  4. 18 years or older.

Exclusion criteria

  1. Previous hematological relapse after first stop of TKI.
  2. Previous AP/BC at any time in the history of the disease.
  3. Restart of TKI without loss of MMR after first stop
  4. Current participation in another clinical study.
  5. Previous or planned allogeneic stem cell transplantation.
  6. Patients with contra-indications to dasatinib therapy due to comorbidities.
  7. Subjects with acute hepatitis B virus (HBV) infections.
  8. Uncontrolled or significant cardiovascular disease.
  9. Pulmonary arterial hypertension.
  10. Pleural or pericardial effusions of any grade at study entry are excluded
  11. History of significant bleeding disorder unrelated to CML
  12. Hypersensitivity to dasatinib and excipients of dasatinib tablets.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

134 participants in 1 patient group

dasatinib
Other group
Description:
2 years of dasatinib treatment before discontinuation if MR 4 is achieved for at least 1 year
Treatment:
Drug: Dasatinib

Trial contacts and locations

21

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Central trial contact

Ulla Olsson-Strömberg, MD PhD; Jeroen JW Janssen, MD PhD

Data sourced from clinicaltrials.gov

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