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A Mixed Methods Study of Medication Adherence in Adults with Neurofibromatosis Type 1 (NF1) on a Clinical Trial of Selumetinib
被引:0
作者:
Curlee, Millicent S.
[1
]
Toledo-Tamula, Mary Anne
[1
]
Baker, Melissa
[1
,3
]
Wikstrom, Daniel
[1
]
Harrison, Cynthia
[1
,4
]
Rhodes, Amanda
[1
]
Fagan, Margaret
[1
]
Tibery, Cecilia
[2
]
Wolters, Pamela L.
[1
]
Widemann, Brigitte C.
[1
]
Gross, Andrea M.
[1
]
Martin, Staci
[1
]
机构:
[1] NCI, Pediat Oncol Branch, Ctr Canc Res, 9030 Old Georgetown Rd, Bethesda, MD 20892 USA
[2] Leidos Biomed Res Inc, Frederick Natl Lab Canc Res, Clin Res Directorate, Frederick, MD 21702 USA
[3] Nova Southeastern Univ, Coll Psychol, Ft Lauderdale, FL 33328 USA
[4] NYU Langone Hlth, NYU Grossman Sch Med, New York, NY 10016 USA
来源:
基金:
美国国家卫生研究院;
关键词:
neurofibromatosis;
plexiform neurofibroma;
selumetinib;
medication adherence;
qualitative interview;
medication event monitoring system;
pill count;
medication diary;
clinical trial;
PLEXIFORM NEUROFIBROMAS;
CHILDREN;
OUTCOMES;
ASSOCIATION;
ADOLESCENTS;
DEPRESSION;
FREQUENCY;
IMPACT;
COHORT;
D O I:
10.3390/cancers17020295
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Oral therapeutic options for plexiform neurofibromas (PNs) in individuals with neurofibromatosis type 1 (NF1) are receiving attention in clinical research. The MEK inhibitor (MEKi) Selumetinib is FDA-approved in children ages 2+ years with inoperable PNs, and shows activity in adults. Prolonged therapy with selumetinib is necessary to maintain tumor reduction. Therefore, investigating long-term adherence is vital to understand patterns of adherence over time and its impact on clinical outcomes. Mixed methods research offers rich information about adherence that can inform future intervention trials, and can assist practitioners in addressing medication adherence concerns. Methods: This mixed-method pilot study is the first examination of the feasibility of a technology-based adherence assessment method, the medication events monitoring system (MEMSTM), among individuals with NF1-PN. Adherence was monitored in a small sample of patients (N = 12; mean age = 34.36 years; 58% male) with NF1 and PN across eighteen 28-day treatment cycles. Qualitative data were obtained from individual interviews using inductive and deductive techniques for thematic analysis. Results: The predetermined criterion was met, suggesting that using MEMSTM is feasible despite some challenges with the caps. Depression and overall stress were significantly related to reduced adherence, although these results should be considered hypothesis-generating. Barriers to medication adherence included forgetting and the timing of doses related to eating. Facilitators included consistency, reminders, and social support. Conclusions: This study highlights patient characteristics that may be related to increased risk for nonadherence, as well as challenges with electronic pill caps that should be considered in future clinical trials for NF1-related PN. Results can inform future adherence interventions for adults with NF1 and PNs. Future research with larger samples is needed to fully explore factors related to long-term medication adherence among individuals with NF1.
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