Multicenter Single-arm Pilot Study Evaluating Efficacy of Nilotinib in CML Patients With Molecular Relapse After Glivec Discontinuation Within the Context of the STIM Trials (STIM and STIM2)
- Conditions
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
- Interventions
- Registration Number
- NCT01774630
- Lead Sponsor
- University Hospital, Bordeaux
- Brief Summary
Chronic myeloid leukemia (CML) is a hematopoietic neoplasm characterized by the reciprocal translocation t(9;22). The resulting oncoprotein, bcr-abl is an essential trigger for growth and survival of leukemic cells. In the past decade, the bcr-abl tyrosine kinase inhibitor (TKI) imatinib (IM or Glivec©) has been the standard of care for patients with CML, inducing durable responses. However, requiring continuing IM indefinitely and the ability of IM to eradicate the CML clone was uncertain.
In a small proportion of patients, IM can induce complete molecular response (CMR) defined by the disappearance of the bcr-abl transcript in conventional quantitative RT-PCR. The question whether or not these patients are cured and can discontinue drug therapy has been assessed by Mahon and coll, in the STIM study. He demonstrates that IM can be safely discontinued in patient with a CMR of at least 2 year duration and all patients who relapsed after IM discontinuation mainly did it in the first 6 months and responded to reintroduction of imatinib.
Nilotinib is a rationally designed second generation tyrosine kinase inhibitor with improved target specificity over imatinib. Its efficacy and safety in the treatment of patients who are resistant or intolerant to imatinib as well as patients with newly diagnosed CML-CP led to the registration in second and first line treatment of CML-CP patients. Nilotinib produces even faster and deeper responses with more occurrence of CMR than does Imatinib. Consequently, one can assume that a more potent drug such nilotinib could induce deeper and sustained CMR allowing longer period off treatment than IM.
The objective of this pilot trial is to assess if Nilotinib can rescue STIM patients in molecular relapse after IM discontinuation and to provide an estimation about duration of CMR after nilotinib discontinuation in 2nd line therapy among patients experiencing 2 years of stable CMR with nilotinib.
- Detailed Description
Patients with CML included in STIM trials, stopped their treatment by imatinib because the signal was not detectable. In case of reappearance of this transcript Bcr-Abl, the patient relapses. The trial Nilo Post STIM is suggested to the patient to assess if Nilotinib can rescue STIM patients in molecular relapse after IM discontinuation and to provide an estimation about duration of CMR after nilotinib discontinuation in 2nd line therapy among patients experiencing 2 years of stable CMR with nilotinib.
The treatment/strategy for this study:
* Screening
* Inclusion/exclusion criteria
* CML history
* Confirm molecular relapse after discontinuation of imatinib (quantitative RT-PCR on two consecutive assessments from peripheral blood samples)
* Treatment
• Nilotinib 300mg BID for 2 years
* Premature treatment discontinuation while on study: primary or secondary resistance progression to accelerated phase or blast crisis, AE (to be defined later).
* In case of unsatisfactory response: transcript stability or increase on two consecutive PCR: nilotinib blood monitoring, and nilotinib dose escalation up to 400mg BID will be proposed
* Discontinuation at 2 years for patients who resumed confirmed CMR
* Follow-up while on treatment with nilotinib:
* Physical exam, basic laboratory parameters, monthly during the first 3 months then every 3 months.
* Centralized quantitative RT-PCR for Bcr-Abl monthly for 6 months then every 3 months for 24 months
* Follow AE management guidelines for nilotinib reduction/interruptions
* Follow-up after nilotinib discontinuation
* Patients in confirmed molecular relapse
* Physical exam, event collection, basic laboratory parameters (including glycemic and lipid profile) every 2 months during the first year then every 3 months
* Hematology and centralized quantitative RT-PCR monthly the first year then every 3 months for 12 months
* Patients without confirmed molecular relapse will take another treatment (dasatinib for example) and will stop their follow-up in the trial
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 31
- Male and female patients
- Patient participating to the STIM trials (including STIM, STIM2 et EURO-SKI) and with confirmed molecular relapse on two consecutive RQ PCR, after imatinib discontinuation
- Still in chronic phase
- Not yet treated for this relapse
- At least 18 years old (no upper age limit)
- SGOT and SGPT < 2.5 UNL
- Serum creatinin < 2 UNL
- No planned allogeneic stem cell transplantation
- Signed informed consent
- ECOG score 0 to 2
- Pregnancy, lactation
- Prior or concurrent malignancy other than CML (exceptions to be mentioned)
- Serious uncontrolled cardiovascular disease
- Severe psychiatric/neurological disease (previous or ongoing)
- Ongoing treatment at risk for inducing "torsades de pointe"
- QTcF > 450ms despite correction of predisposing factors (i.e electrolytes...)
- Congenital long QTcF
- No health insurance coverage
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Nilotinib Nilotinib 300 mg/twice a day
- Primary Outcome Measures
Name Time Method Estimated survival rate of patients without molecular relapse 3 years after enrollment Evaluation by RTq-PCR monthly the first year of treatment with nilotinib then every 3 months until 24 months, date of discontinuation of Nilotinib for patients in sustained complete molecular response (CMR). After discontinuation of Nilotinib patie CMR is defined as \>5 log reduction in Bcr-Abl and Abl levels and undetectable transcripts on quantitative RTq-PCR
- Secondary Outcome Measures
Name Time Method Event free survival (EFS) Overall and after nilotinib discontinuation Same events as for EFS described above
Rate and kinetics of CMR while on treatment with nilotinib at 6 and 12 months of treatment with nilotinib Same definition of CMR as above
Safety tolerability of nilotinib and compliance Any time Haematological and non-haematological adverse events (AE) graded will be according to the NCI CTC AE v4. Compliance will be estimated using the 4 items Morisky scale
Duration of CMR while on treatment with nilotinib Any time Defined as the time from the date of first documented CMR to the date of first confirmed molecular relapse defined as positivity of Bcr-Abl transcripts in quantitative RT-PCR with a ratio of bcr-abl to Abl ≥ 10-5, as confirmed by a second analysis point at two successive assessments
Duration of CMR after nilotinib discontinuation Measured from the start of nilotinib discontinuation to the date of first confirmed molecular relapse as defined above Predictive factors of maintained CMR after nilotinib discontinuation: sex, Sokal risk score at diagnosis, duration of previous treatment with imatinib, CMR duration before and after discontinuation of imatinib After discontinuation of nilotinib Parameters will be recorded before and after both sequences of treatment imatinib and nilotinib
Trial Locations
- Locations (10)
Centre Hospitalier Lyon Sud, Service Hématologie
🇫🇷Pierre Benite, France
CHU de Toulouse, Service d'Hématologie
🇫🇷Toulouse, France
Centre Hospitalier de Versailles - Hôpital André Mignot - Service de Médecine B
🇫🇷Le Chesnay, France
Hôpital Haut Lévêque, Service Hématologie
🇫🇷Pessac, France
Institut Bergonié
🇫🇷Bordeaux, France
CHU de Nice, Service Hématologie Clinique
🇫🇷Nice, France
CHU Angers
🇫🇷Angers, France
CH Valence
🇫🇷Valence, France
Hôpital Pontchaillou
🇫🇷Rennes, France
CH d'Annecy
🇫🇷Pringy, France