Abstract | MAIN PURPOSE: RESEARCH QUESTIONS: Is single agent voreloxin active in preclinical models of AML? Does the combination of voreloxin and cytarabine enhance the activity of either agent alone? METHODS: Inhibition of proliferation was studied in three cancer cell lines: HL-60 ( acute promyelocytic leukemia), MV4-11 (AML), and CCRF-CEM ( Acute lymphoblastic leukemia). Combination index (CI) analysis established the effect of the drugs in combination. A mouse model of bone marrow ablation was used to investigate in vivo efficacy of the drugs alone and in combination. Peripheral white blood cell and platelet counts were followed to assess marrow impact and recovery. RESULTS:
Voreloxin and cytarabine alone and in combination exhibited cytotoxic activity in human leukemia cell lines and in vivo. The two drugs had additive or synergistic activity in vitro and supra-additive activity in vivo. Bone marrow ablation was accompanied by reductions in peripheral white blood cells and platelets that were reversible within 1 week, consistent with the AML treatment paradigm. CONCLUSIONS: These data support ongoing clinical evaluation of voreloxin both alone and in combination with cytarabine for the treatment of AML.
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Authors | Caroline D Scatena, Jeffrey L Kumer, Jennifer P Arbitrario, Anthony R Howlett, Rachael E Hawtin, Judith A Fox, Jeffrey A Silverman |
Journal | Cancer chemotherapy and pharmacology
(Cancer Chemother Pharmacol)
Vol. 66
Issue 5
Pg. 881-8
(Oct 2010)
ISSN: 1432-0843 [Electronic] Germany |
PMID | 20058009
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Naphthyridines
- Thiazoles
- Cytarabine
- vosaroxin
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Topics |
- Animals
- Antineoplastic Combined Chemotherapy Protocols
(pharmacology)
- Blood Platelets
(drug effects, metabolism)
- Bone Marrow Cells
(drug effects, metabolism)
- Cell Proliferation
(drug effects)
- Cytarabine
(administration & dosage)
- Disease Models, Animal
- Drug Synergism
- Female
- HL-60 Cells
- Humans
- Leukemia, Promyelocytic, Acute
(drug therapy, pathology)
- Leukocytes
(drug effects, metabolism)
- Mice
- Naphthyridines
- Precursor Cell Lymphoblastic Leukemia-Lymphoma
(drug therapy, pathology)
- Thiazoles
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