PMID- 29095654 OWN - NLM STAT- MEDLINE DCOM- 20190415 LR - 20220114 IS - 1473-4877 (Electronic) IS - 0300-7995 (Linking) VI - 34 IP - 2 DP - 2018 Feb TI - Incidence of type 2 diabetes mellitus and hyperlipidemia in patients prescribed dasatinib or nilotinib as first- or second-line therapy for chronic myelogenous leukemia in the US. PG - 353-360 LID - 10.1080/03007995.2017.1399870 [doi] AB - OBJECTIVE: Evaluate the incidence of type 2 diabetes mellitus (T2DM) and hyperlipidemia (HLD) in CML patients initiating therapy with dasatinib or nilotinib. METHODS: Retrospective study using MarketScan claims from January 2006 to December 2014. The first analysis evaluated occurrence of T2DM, defined as >/=2 claims with a T2DM ICD-9 code or 1 diagnosis claim and an antidiabetic medication. The second analysis evaluated occurrence of HLD, defined as >/=2 claims with an HLD ICD-9 code, or 1 diagnosis claim and an anti-HLD medication. Incidence rates were computed as number of events divided by sum of person years (PY) at risk for all subjects. Multivariate Cox proportional hazards models estimated hazard ratios (HRs) for T2DM or HLD. RESULTS: There were 2004 and 1280 patients who met the criteria for the T2DM analysis (n = 1272 dasatinib, n = 732 nilotinib) and HLD analysis (n = 845 dasatinib, n = 435 nilotinib). The incidence rate of T2DM was 40.4 per 1000 PY (95% CI: 27.60, 56.98) for nilotinib and 17.6 per 1000 PY (95% CI: 11.14, 26.38) for dasatinib. HR for occurrence of T2DM was 2.77 (95% CI: 1.58, 4.86), indicating that patients on nilotinib had a significantly higher adjusted risk for incident T2DM. The incidence rate of HLD was 74.6 per 1000 PY (95% CI: 50.70, 105.94) for nilotinib and 46.4 per 1000 PY (95% CI: 33.00, 63.45) for dasatinib. HR for occurrence of HLD was 1.75 (95% CI: 1.07, 2.87) indicating that patients on nilotinib had a significantly higher adjusted risk for incident HLD. CONCLUSIONS: Patients receiving nilotinib had significantly higher rates of incident T2DM or HLD than patients on dasatinib. FAU - Franklin, Meg AU - Franklin M AD - a Franklin Pharmaceutical Consulting LLC , Rock Hill , SC , USA. FAU - Burns, Leah AU - Burns L AD - b Center for Observational Research and Data Sciences , Princeton , NJ , USA. FAU - Perez, Samuel AU - Perez S AD - c Mu Sigma , Northbrook , IL , USA. FAU - Yerragolam, Deepak AU - Yerragolam D AD - d Mu Sigma Business Solutions , Karnataka , India. FAU - Makenbaeva, Dinara AU - Makenbaeva D AD - e Bristol-Myers Squibb Company , Princeton , NJ , USA. LA - eng PT - Journal Article PT - Observational Study PT - Research Support, Non-U.S. Gov't DEP - 20171130 PL - England TA - Curr Med Res Opin JT - Current medical research and opinion JID - 0351014 RN - 0 (Protein Kinase Inhibitors) RN - 0 (Pyrimidines) RN - F41401512X (nilotinib) RN - RBZ1571X5H (Dasatinib) SB - IM MH - Adult MH - Aged MH - Correlation of Data MH - *Dasatinib/administration & dosage/adverse effects MH - Diabetes Mellitus, Type 2/*epidemiology MH - Female MH - Humans MH - Hyperlipidemias/*epidemiology MH - Incidence MH - Insurance Claim Review MH - *Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy/epidemiology MH - Male MH - Middle Aged MH - Proportional Hazards Models MH - Protein Kinase Inhibitors/administration & dosage/adverse effects MH - *Pyrimidines/administration & dosage/adverse effects MH - Retrospective Studies MH - Risk Assessment MH - United States/epidemiology OTO - NOTNLM OT - CML OT - hyperlipidemia OT - metabolic outcomes OT - type 2 diabetes mellitus OT - tyrosine kinase inhibitors EDAT- 2017/11/03 06:00 MHDA- 2019/04/16 06:00 CRDT- 2017/11/03 06:00 PHST- 2017/11/03 06:00 [pubmed] PHST- 2019/04/16 06:00 [medline] PHST- 2017/11/03 06:00 [entrez] AID - 10.1080/03007995.2017.1399870 [doi] PST - ppublish SO - Curr Med Res Opin. 2018 Feb;34(2):353-360. doi: 10.1080/03007995.2017.1399870. Epub 2017 Nov 30.