Adherence trajectories in oral therapy for chronic myeloid leukemia: Overview of a research protocol.
Adherence trajectories in oral therapy for chronic myeloid leukemia: Overview of a research protocol.
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慢性髓样白血病的口服治疗中的依从性轨迹:研究方案的概述。
DOI:
10.1002/nur.22069
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发表时间:
2020-09
影响因子:
2
通讯作者:
Jennings BM
中科院分区:
文献类型:
--
作者:
Yeager KA;Waldrop-Valverde D;Paul S;Bruner DW;Klisovic R;Burns E;Mason TA;Patel N;Jennings BM
Over a quarter of chemotherapy regimens now include oral agents. Individuals living with cancer are now responsible for administering this lifesaving therapy at home by taking every dose as prescribed. One type of oral chemotherapy, tyrosine kinase inhibitors (TKIs), is the current recommended treatment for chronic myeloid leukemia. This targeted therapy has markedly improved survival but comes with significant side effects and financial costs. In the study described in this protocol, the investigators seek to understand the dynamic nature of TKI adherence experienced by individuals diagnosed with CML. Using a mixed method approach in this prospective observational study, funded by the National Cancer Institute, we seek to describe subjects’ adherence trajectories over one year. We aim to characterize adherence trajectories in individuals taking TKIs using model-based cluster analysis. Next, we will determine how side effects and financial toxicity influence adherence trajectories. Then we will examine the influence of TKI adherence trajectories on disease outcomes. Additionally, we will explore the experience of patients taking TKIs by interviewing a subset of participants in different adherence trajectories. The projected sample includes 120 individuals taking TKIs who we will assess monthly for 12 months, measuring adherence with an objective measure (Medication Event Monitoring System- MEMS®). Identifying differential trajectories of adherence for TKIs is important for detecting subgroups at the highest risk of nonadherence and will support designing targeted interventions. Results from this study can potentially translate to other oral agents to improve care across different types of cancer.
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影响因子:
28.4
作者:
Dueck AC;Mendoza TR;Mitchell SA;Reeve BB;Castro KM;Rogak LJ;Atkinson TM;Bennett AV;Denicoff AM;O'Mara AM;Li Y;Clauser SB;Bryant DM;Bearden JD 3rd;Gillis TA;Harness JK;Siegel RD;Paul DB;Cleeland CS;Schrag D;Sloan JA;Abernethy AP;Bruner DW;Minasian LM;Basch E;National Cancer Institute PRO-CTCAE Study Group
通讯作者:
National Cancer Institute PRO-CTCAE Study Group
影响因子:
3.2
作者:
Hsieh, HF;Shannon, SE
通讯作者:
Shannon, SE
影响因子:
6.2
作者:
de Souza JA;Yap BJ;Wroblewski K;Blinder V;Araújo FS;Hlubocky FJ;Nicholas LH;O'Connor JM;Brockstein B;Ratain MJ;Daugherty CK;Cella D
通讯作者:
Cella D
影响因子:
1.3
作者:
Anderson, Kristin R.;Chambers, Carole R.;Sheikh, Naureen
通讯作者:
Sheikh, Naureen
影响因子:
1.8
作者:
Komarek, Arnost;Komarkova, Lenka
通讯作者:
Komarkova, Lenka