Azacytidine for the Treatment of Myelodysplastic Syndromes/Acute Myeloid Leukemia (MDS/AML) With High Risk (Chromosome 7 and or Complex) Cytogenetic Abnormalities

NCT ID: NCT00915785

Last Updated: 2013-04-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-11-30

Brief Summary

The purpose of this study is to assess the hematological and cytogenetic responses with 5 azacytidine in patients over 55 years of age with MDS/AML due to chromosome 7 abnormalities and to assess the hematological and cytogenetic response rates in patients with relapsed AML and chromosome 7 abnormality.

Conditions

Myelodysplastic Syndromes; Leukemia, Myeloid, Acute

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

5 azacytidine

Group Type: EXPERIMENTAL

5 azacytidine

Intervention Type: DRUG

Patients will receive azacytidine 75 mg/m2/day SC for 7 days every 28 days for up to 6 cycles, unless they are discontinued from the treatment.

Interventions

5 azacytidine

Patients will receive azacytidine 75 mg/m2/day SC for 7 days every 28 days for up to 6 cycles, unless they are discontinued from the treatment.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Abnormalities to chromosome 7, including monosomy 7 either alone or as part of a complex clone.
• Be > 55 years of age; younger if first or subsequent relapse in patient less < 55 years but with a chromosome 7 abnormality alone or as part of a complex clone.
• Have an International Prognostic Scoring System (IPSS) score of INT 1.5 and a diagnosis of RAEB or RAEB-T per French-American-British (FAB) classification criteria or a diagnosis of Myelodysplastic CMMoL per modified FAB criteria meeting the following:

• Monocytosis in peripheral blood > 1x109/L;
• Dysplasia in one or more myeloid cell lines;
• 10% to 29% blasts in the BM;
• White blood cell (WBC) < 13,000 x109/L;
• Have a life expectancy of at least 3 months;
• Have an Eastern Cooperative Oncology Group (ECOG) Performance Status Grade of 0-2.
• Have serum bilirubin levels of at least 1.5 x the upper limit of the normal range for the laboratory (ULN). Higher levels are acceptable if these can be attributed to:

• active hemolysis (as indicated by positive direct Coombs' testing);
• decreased or absent haptoglobin level;
• elevated indirect bilirubin and/or lactate dehydrogenase [LDH]); or
• ineffective erythropoiesis (as indicated by bone marrow findings).
• Have serum glutamic-oxaloacetic transaminase (SGOT) (aspartate aminotransferase [AST]) or serum glutamic-pyruvic transaminase (SGPT) (alanine aminotransferase [ALT]) levels of at least 2 x ULN.
• Have serum creatinine levels of at least 1.5 x ULN.
• Women of childbearing potential may participate, providing they meet the following conditions:

• must agree to use at least 2 effective contraceptive methods throughout the study and for 3 months following the date of the last dose of study medication;
• must have a negative serum pregnancy test obtained within 24 hours prior to Day 1.
• Males with female partners of childbearing potential must agree to use at least 2 effective contraceptive methods throughout the study and should avoid fathering a child for 6 months following the date of the last dose of study medication.
• Be able to provide written informed consent.

Exclusion Criteria

• Prior treatment with azacitidine.
• Diagnosis of malignant disease within the previous 12 months (excluding basal cell carcinoma with no complications).
• Diagnosis of metastatic disease.
• Previous diagnosis of hepatic tumors.
• Radiation therapy, chemotherapy, or cytotoxic therapy, given to treat conditions other than MDS/AML and administered within the previous 12 months prior to the first day of treatment (Day 1).
• Known or suspected hypersensitivity to azacitidine or mannitol.
• Prior or active disease that, in the opinion of the Investigator, may interfere with the procedures or evaluations to be conducted in the study.
• Serious medical illness likely to limit survival to under or equal to 12 months after screening or likely to prevent granting of informed consent (e.g., history of severe congestive heart failure, clinically unstable cardiac disease, or pulmonary disease).
• Psychiatric illness that would prevent granting of informed consent;
• Treatment with erythropoietin or myeloid growth factors (granulocyte colony-stimulating factor [G-CSF] or granulocyte-macrophage colony-stimulating factor [GM-CSF]) during the previous 21 days prior to Day 1.
• Treatment with androgenic hormones during the previous 14 days prior to Day 1.
• Active viral infection with known human immunodeficiency virus (HIV) or viral hepatitis type B or C.
• Treatment with other investigational drugs within the previous 30 days prior to Day 1, or ongoing adverse events from previous treatment with investigational drugs, regardless of the time period.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

King's College London

OTHER

Sponsor Role: lead

Responsible Party

King's College London

Principal Investigators

Ghulam J Mufti, MB, DM, FRCP, FRCPath

Role: PRINCIPAL_INVESTIGATOR

King's College London

Locations

King's College Hospital NHS Foundation Trust

London, , United Kingdom

Countries

United Kingdom

Other Identifiers

REC - 05/Q0703/168

Identifier Type: -

Identifier Source: secondary_id

EudraCT - 2005-003732-22

Identifier Type: -

Identifier Source: secondary_id

05CC12

Identifier Type: -

Identifier Source: org_study_id