medication adherence molecular monitoring and clinical outcomes in patients with chronic myelogenous leukemia in a large hmo

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medication adherence molecular monitoring and clinical outcomes in patients with chronic myelogenous leukemia in a large hmo

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SCIENCE AND PRACTICE Journal of the American Pharmacists Association xxx (2017) 1e8 Contents lists available at ScienceDirect Journal of the American Pharmacists Association journal homepage: www.japha.org RESEARCH Medication adherence, molecular monitoring, and clinical outcomes in patients with chronic myelogenous leukemia in a large HMO Reina Haque*, Jiaxiao Shi, Joanie Chung, Xiaoqing Xu, Chantal Avila, Christopher Campbell, Syed A Ahmed, Lei Chen, Joanne E Schottinger a r t i c l e i n f o a b s t r a c t Article history: Received 11 July 2016 Accepted 10 January 2017 Objective: Our objective was to examine the association between adherence to tyrosine kinase inhibitors (TKIs) and molecular monitoring and the risk of disease progression or mortality among patients with chronic phase chronic myeloid leukemia (CML) Design: We assembled a retrospective cohort of patients with CML (chronic phase, no prior cancer history, and confirmed to be Philadelphia chromosome positive) using data from electronic health records and chart reviews Medication possession ratio (MPR) was used to measure drug adherence Setting: A large, community-based, integrated health plan in Southern California Participants: The cohort consisted of 245 adult patients (18 years old) with Philadelphia positive chronic phase CML diagnosed from 2001 to 2012 and followed through 2013 Main outcome measures: In survival analyses, we examined the association of TKI adherence (MPR) and polymerase chain reaction (PCR) monitoring test frequency with the composite clinical outcome, progression to accelerated phase diseaseeblast crisis or mortality (progression-free survival) The cohort was followed for a maximum of 13 years (median 4.6 years) Results: Over 90% of the cohort initiated TKI therapy within months of diagnosis, and the mean MPR was 88% (SD 18%) Virtually all patients (96%) started on imatinib The rates of progression to accelerated phaseeblast crisis and mortality were lower in patients with greater TKI adherence (20.4/1000 person-years) versus lower adherence (27.0/1000 personyears) Patients who underwent PCR monitoring had a significantly reduced risk of progression or mortality, which was seen in patients with high and low TKI adherence status from both the groups (hazard ratio [HR] 0.07 [95% CI 0.03-0.19 if MPR >90%] and HR 0.70 [95% CI 0.02-0.21 if MPR

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