The main goal of the study is the assessment of duration of major molecular response (MMR) or better at 12 and 36 months after stopping tyrosine kinase inhibitors (TKI) therapy a second or third time in patients with at least three years prior TKI treatment comprising at least two years of nilotinib treatment within this trial and maintained stable MR4 (BCR-ABL ratio \<0,01% on international Scale (IS) for at least one year and MR4.5 (BCR-ABL ratio \<0,0032% on IS) for at least 6 months: * who failed a first stop in the EURO-SKI study (standardized criteria) * who failed a first or second stop outside the EURO-SKI study but would have had fulfilled same eligible criteria and were stopped according to EURO-SKI rules * who failed a first or second stop outside the EURO-SKI study without fulfilling EURO-SKI rules
The proposal is to re-treat patients with a minimum of two years with nilotinib 2x300 mg/d resulting in total of at least three years TKI treatment who show recurrent disease after unsuccessful first or second stop after TKI treatment in or outside the EURO-SKI study. If MR4 or better is re-achieved and maintained for at least one year and MR4.5 or better is re-achieved and maintained for at least 6 months, patients will be eligible for a second stop attempt within this study. For MR4, three consecutive PCRs with MR4 or deeper should be measured within one year and for MR4.5, two PCRs during 6 months should demonstrate a MR4.5. Patients who exhibited hematological relapse after the first stop attempt will not be eligible for a second stop attempt within this study. After inclusion, 3 monthly monitoring will be performed under nilotinib treatment within the trial. Patients fulfilling the criteria mentioned above will then enter the screening phase. After verification of MR4.5, TKI treatment will be stopped and patients followed in the same manner as described in EURO-SKI (monthly PCRs for 6 months, 6-weekly PCRs 7-12 months after stopping, thereafter 3-monthly). If MMR is lost (BCR-ABL \>0.1% (IS)), TKI treatment will once again be restarted; here the same TKI (nilotinib) is recommended. It is assumed that after failure of first (or second) stop a switch to treatment with 2GTKI may increase the chance of stopping a second (or third) time \[Legros et al. Blood 2012; Rea et al. Blood 2014\] It is expected that the rate of a successful second (or third) stop at 12 and 36 months is more than 25%.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
75
2nd or 3rd TKI stop after pre-treatment with nilotinib.
Pre-treatment with nilotinib 300 mg/bid for 2 years
Universitätsklinikum Freiburg
Freiburg im Breisgau, Baden-Wurttemberg, Germany
Universitätsmedizin Mannheim
Mannheim, Baden-Wurttemberg, Germany
Klinikum rechts der Isar
München, Bavaria, Germany
Medizinische Hochschule Hannover
Hannover, North Rhine-Westphalia, Germany
Universitätsklinikum der RWTH
Aachen, Germany
Klinikum Bayreuth
Bayreuth, Germany
Klinikum Chemnitz
Chemnitz, Germany
Onkologische Schwerpunktpraxis
Esslingen am Neckar, Germany
Universitätsklinikum Halle (Saale)
Halle, Germany
Schwerpunktpraxis Onkologie
Heilbronn, Germany
...and 5 more locations
Assessment of duration of MMR or better at 12 months after stopping TKI therapy a second or third time
Assessment of duration of MMR or better at 12 months after stopping TKI therapy a second time in patients with at least three years prior TKI treatment comprising at least two years of nilotinib treatment within this trial and maintained stable MR4 for at least one year and MR4.5 for at least 6 months
Time frame: 12 months after stopping
Assessment of quality of life (QoL) profiles under nilotinib treatment and comparison with previous TKI therapy before switch and after stopping
To investigate QoL changes over time in relapse-free patients without TKI re-start as measured by the EORTC QLQ-C30 and CML 24 (one combined questionnaire)
Time frame: 5 years
Identification of clinical and biological factors correlating with the persistence of MMR or better after stopping TKI
Proportion of high risk patients according to the risk score at 6 months after stopping TKI;
Time frame: 6 months after stopping
Estimation of overall survival
Overall survival is calculated from the date of 2nd stop of TKI treatment until the date of death irrespective of the cause of death. Patients still alive at the date of analysis will be censored at the date of last follow-up.
Time frame: 3 years
Time to re-achievement of MR4.5 after restart of therapy
Assessment of molecular response after 3 years
Time frame: 3 years
Number of patients with grade 1 through grade 5 adverse events (AEs) that are related to study drug, graded according to NCI CTCAE Version 3.0
Assessment of incidence of any AEs (e.g. from musculoskeletal system) that arise after stopping TKI treatment a second time
Time frame: 3 years
Assessment of duration of MMR or better
Assessment of duration of MMR or better at 36 months after stopping TKI therapy a second or third time in patients with at least three years prior TKI treatment comprising at least two years of nilotinib treatment
Time frame: 36 months after stopping
Number of patients with grade 1 through grade 5 adverse events (AEs) that are related to study drug, graded according to NCI CTCAE Version 3.0
Assessment of incidence of any AEs (e.g. from musculoskeletal system) that arise after stopping TKI treatment a second time
Time frame: 2 years treatment with nilotinib 300 mg/bid
Estimation of progression-free survival
Progression-free survival is defined as overall survival plus the additional events progression to accelerated phase or blast crisis that also terminate PFS
Time frame: 3 years
Identification of clinical and biological factors correlating with the persistence of MMR or better after 6 months
Proportion of female patients without molecular relapse
Time frame: 6 months after stopping
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