Phase II Clofarabine and Cytarabine for Newly Diagnosed Acute Myeloid Leukemia

• Status: Terminated
• Trial end date: 2015-03-01
• Target enrollment: 0
• Participant gender: All

Summary

The combination of clofarabine and cytarabine is an effective and reasonably well-tolerated treatment regimen in patients with either relapsed/refractory or newly diagnosed AML. For this prospective study, we propose the use of clofarabine and cytarabine for second course induction therapy for patients with persistent AML after treatment with an anthracycline and cytarabine.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University of Pittsburgh
• Treatments: Antimetabolites; Clofarabine; Cytarabine

Criteria

Inclusion Criteria:

1. Patients with newly diagnosed AML based on the World Health Organization classification who have persistent disease after their first course treatment with an anthracycline and cytarabine

2. Able to understand and have the ability to provide written informed consent

3. Patients over 18 years of age

4. Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2

5. Left ventricular ejection fraction (LVEF) ≥ 50%

6. Negative urine pregnancy test for all females

7. All subjects must agree to use an effective method of contraception while receiving the study drugs

Exclusion Criteria:

1. Diagnosis of acute promyelocytic leukemia

2. Relapsed AML

3. Prior use of clofarabine

4. Previous allogeneic or autologous hematopoietic cell transplantation

5. Impaired liver function (serum total bilirubin > 2.0 mg/dL, alanine aminotransferase and aspartate aminotransferase ≥ 4 x the upper limit of normal)

6. Impaired renal function (serum creatinine ≥ 2.0 mg/dL)

7. Uncontrolled or life-threatening infection that is not responding to antimicrobial therapy

8. History of a psychiatric disorder which may compromise compliance with the protocol or which does not allow for appropriate informed consent

9. Concurrent active malignancy; exceptions include patients who have been disease free for 5 years, patients with a history of completely resected non-melanoma skin cancer or successfully treated in situ carcinoma, or patients with another malignancy that is indolent or definitively treated

10. Evidence of severe or uncontrolled systemic diseases (e.g., unstable or uncompensated respiratory or cardiac disease)