Efficacy and Safety of Dose Redution of Radotinib as a First Line Treament in Ph+ CML

Exclusion Criteria

• •1. Patients with Philadelphia chromosome negative
• •2. Patients who used Radotinib for 8 days or longer before study entry
• •3. Patients who had been treated with other targeted anti-cancer therapy, except for Hydrea or Agrylin, which inhibits the growth of leukemic cells
• •4. Patients who have hypersensitivity to active ingredient or any of the excipients of this investigational product.
• •5. Patients with impaired cardiac function as defined below:
• •* Patients who cannot have QT intervals measured according to ECG
• •* Complete left bundle branch block
• •* Patients with cardiac pacemakers
• •* Patients with congenital long QT syndrome or the family history of known long QT syndrome
• •* The mean QTcF \>450msec ECG tests at baseline
• •* Clinically significant resting bradycardia (\< 50 bpm) History of, or presence of symptomatic ventricular or atrial tachyarrhythmias
• •* Clinically significant resting bradycardia (\< 50 bpm)
• •* Medical history of clinically confirmed myocardial or infarctionof unstable angina (within last 12 months)
• •* Other clinically significant cardiac disease (e.g. congestive heart failure, or uncontrolled hypertension)
• •6. Cytologically confirmed CNS involvement (if asymptomatic, spinal fluid examination is not necessary prior to first treatment)
• •7. Severe or uncontrolled chronic medical condition (e.g., uncontrolled diabetes, active or uncontrolled infection)
• •8. Other significant congenital or acquired bleeding disorders that are not related to underlying leukemia
• •9. Patients who previously received radiotherapy to at least 25% of the bone marrow
• •10. Patients who had a major surgery within 4 weeks prior to study entry or has not recovered from side effects of such surgery
• •11. Patients who diagosed with another clinically significant malignant tumor wihin 5years before study etnry, excluding basal cell carcinoma
• •12. Patients who are currently receiving treatment with a strong CYP3A4 inhibitor (e.g., erythromycin, ketoconazole, itraconazole, voriconazole, clarithromycin, telithromycin, ritonavir, mibefradil) or CYP3A4 inducer (e.g., dexamthasone, phenytoin, carbamazepine, rifampin, rifabutin, rifapentin, phenobarbitol, St. John's Wort). Treatment cannot be safely discontinued or switched to a different medication prior to initiation of study treatment
• •13. Patients who are currently receiving treatment with a medication that has the potential to prolong the QT interval. Treatment cannot be safely discontinued or switched to a different medication prior to initiation of study treatment
• •14. Impairment of GI function or GI disease that may significantly alter absorption of study drugs (e.g., ulcerative colitis, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, small bowel resection, GI bypass surgery).
• •15. History of acute or chronic pancreatitis within last one year
• •16. Acute or chronic liver or pancreas disease or severe renal disease
• •17. Patients with HbsAg, HCV Ab positive
• •* following subjects can be enrolled.
• •* Inactive hepatitis B surface antigen (HBsAg) carriers(site specific local lab normal range lower limit assessed by investigator)
• •* undergoding HCV Ab or HCV RNA testing judged by investigator to be eligible for enroll
• •18. History of HIV Ab positive or confirmed HIV Ab positvie.
• •19. Pregnant or the women with breast-feeding 2