Low dose combination CDA substrate drug/cedazuridine with extended administration
This invention relates to methods and compositions for administering an effective amount of a CDA substrate drug and an effective amount of cedazuridine. In particular, the invention relates to methods for treating cancer, inhibiting degradation of a CDA substrate drug, and reducing DNA methylation in a subject in need thereof comprising administering an effective amount of a CDA substrate drug and an effective amount of cedazuridine.
1. A method for treating cancer in a subject in need thereof, wherein said cancer is myelodysplastic syndromes (MDS), leukemia, or lymphoma, comprising administering to the subject:
(i) decitabine at a dose of about 5 mg to about 15 mg; and
(ii) an effective amount of cedazuridine,
thereby treating cancer in the subject.
2. The method of claim 1 , wherein the leukemia is acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic myeloid leukemia (CML), myeloproliferative neoplasms (MPN), or chronic myelomonocytic leukemia (CMML).
3. The method of claim 1 , wherein the MDS is International Prognostic Scoring System (IPSS) low and/or IPSS intermediate 1 MDS.
4. The method of claim 1 , wherein the administering is performed in one composition.
5. The method of claim 1 , wherein the decitabine is administered at a cumulative dose of from about 15 mg to about 75 mg cumulative per 28-day cycle of treatment.
6. The method of claim 1 , wherein the effective amount of cedazuridine is from about 40 mg per dose to about 1000 mg per dose.
7. The method of claim 1 , wherein the effective amount of cedazuridine is from about 100 mg to about 7000 mg cumulative per 28-day cycle of treatment.
8. The method of claim 1 , wherein the administering reduces absolute neutrophil count (ANC) in the subject to less than 0.5×10 9 cells/L for no more than two weeks following a 28-day cycle of treatment.
9. The method of claim 1 , wherein the administering expands hemoglobin F-expressing.
10. The method of claim 1 , wherein the administering reduces DNA methylation in the subject by at least 5% as compared to DNA methylation in the subject prior to the administering.