Stem Cell Monitoring for CML Patients Undergoing Nilotinib Therapy

Inclusion Criteria:

Patients 18 years or older
Eastern Cooperative Oncology Group (ECOG) Performance status 0,1, or 2

Documented diagnosis of Ph+ Chronic phase CML:

Chronic phase: None of the criteria for accelerated or blastic phase

Accelerated phase

Blasts ≥ 15% in blood or BM
Blasts plus progranulocytes ≥ 30% in blood or bone marrow (BM)
Basophilia ≥ 20% in blood or BM
Platelets < 100 × 109/L unrelated to therapy
Cytogenetic clonal evolution

Blast phase

≥ 30% blasts in blood or BM
Extramedullary disease with localized immature blasts

Adequate end organ function, defined as the following:

Creatinine < 1.5 x upper limit of normal (ULN)
Absolute neutrophil count (ANC) > 1.5 x 109/L
Platelets > 100 x 109/L
Total bilirubin < 1.5 x ULN (Does not apply to patients with isolated hyperbilirubinemia [e.g., Gilbert's disease] grade <3)
Aspartate aminotransferase (AST) (SGOT) and Alanine aminostransferase (ALT) (SGPT) < 3 x ULN
Serum amylase and lipase ≤ 2 x ULN
Alkaline phosphatase ≤ 2.5 x ULN

Patients must have the following laboratory values (WNL = within normal limits at the local institution lab) or corrected to within normal limits with supplements prior to the first dose of study medication:

Potassium (WNL)
Magnesium (WNL)
Phosphorus (WNL)
Calcium (WNL)

Exclusion Criteria:

Previous treatment with any other tyrosine kinase inhibitor except for up to 2 weeks of nilotinib

Impaired cardiac function including any one of the following:

Inability to monitor the QT interval on ECG
Congenital long QT syndrome or a known family history of long QT syndrome.
Clinically significant resting brachycardia (<50 beats per minute)
Q-T Corrected (corrected Q-T interval) (QTc) > 450 msec on baseline ECG. If QTc >450 msec and electrolytes are not within normal ranges, electrolytes should be corrected and then the patient re-screened for QTc
Myocardial infarction within 12 months prior to starting study Other clinically significant uncontrolled heart disease (e.g. unstable angina, congestive heart failure or uncontrolled hypertension)
History of or presence of clinically significant ventricular or atrial tachyarrhythmias
Complete left bundle branch block
Right bundle branch block plus left anterior/posterior hemiblock
Use of ventricular-paced pacemaker
History of unstable angina within 1 year of study entry
Patients currently receiving treatment with strong CYP3A4 inhibitors and treatment cannot be either discontinued or switched to a different medication prior to starting study drug. (http://medicine.iupui.edu/clinpharm/ddis/) ).
Patients currently receiving treatment with any medications that have the potential to prolong the QT interval and the treatment cannot be either discontinued or switched to a different medication prior to starting study drug (http://crediblemeds.org/)
Impaired gastrointestinal (GI) function or GI disease that may significantly alter the absorption of study drug (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, small bowel resection or gastric bypass surgery).
History of acute pancreatitis within 1 year of study entry or past medical history of chronic pancreatitis
Severe and/or uncontrolled concurrent medical disease that in the opinion of the investigator could cause unacceptable safety risks or compromise compliance with the protocol (e.g. uncontrolled diabetes, uncontrolled infection)
History of another active malignancy within 5 years prior to study entry with the exception of previous or concomitant basal cell skin cancer and previous carcinoma in situ treated curatively
Known presence of significant congenital or acquired bleeding disorder unrelated to cancer
Major surgery within 4 weeks prior to Day 1 of the study or who have not recovered from prior surgery
Treatment with other investigational agents within 30 days of Day 1.
Pregnant or nursing (lactating) women, where pregnancy is defined as the state of female after conception and until the termination of gestation, confirmed by a positive Human chorionic gonadotropin (hCG) laboratory test. Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during the study and for 14 days after the final dose of nilotinib.