A study of donepezil in female breast cancer survivors with self-reported cognitive dysfunction 1 to 5 years following adjuvant chemotherapy

被引:64
|
作者
Lawrence, J. A. [1 ,5 ]
Griffin, L. [1 ]
Balcueva, E. P. [2 ]
Groteluschen, D. L. [3 ]
Samuel, T. A. [4 ]
Lesser, G. J. [1 ,5 ]
Naughton, M. J. [1 ]
Case, L. D. [1 ]
Shaw, E. G. [1 ]
Rapp, S. R. [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC 27157 USA
[2] Michigan CCOP, Saginaw, MI 48602 USA
[3] St Vincent CCOP, Green Bay Oncol, Green Bay, WI 54301 USA
[4] Med Coll Georgia MBCCOP, Augusta, GA 30912 USA
[5] Wake Forest Univ, Bowman Gray Sch Med, Dept Hematol & Oncol, Winston Salem, NC 27157 USA
关键词
Cognitive dysfunction; Breast cancer survivors; Donepezil; Memory; QUALITY-OF-LIFE; PHASE-II; WOMEN; FATIGUE; STATES; ASSOCIATION; PERFORMANCE; IMPAIRMENT; PREVALENCE; DEMENTIA;
D O I
10.1007/s11764-015-0463-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Some breast cancer survivors report cognitive difficulties greater than 1 year after chemotherapy. Acetylcholinesterase inhibitors (AChEI) may improve cognitive impairment. We conducted a randomized, placebo-controlled, pilot study to assess the feasibility of using the AChEI, donepezil, to improve subjective and objective measures of cognitive function in breast cancer survivors. Women who received adjuvant chemotherapy 1-5 years prior with current cognitive dysfunction symptoms were randomized to 5 mg of donepezil/day vs placebo for 6 weeks and if tolerated 10 mg/day for 18 weeks for a total of 24 weeks. A battery of validated measures of attention, memory, language, visuomotor skills, processing speed, executive function, and motor dexterity and speed was administered at baseline and at 24 and 36 weeks. Subjective cognitive function, fatigue, sleep, mood, and health-related quality of life were evaluated at baseline and at 12, 24, and 36 weeks. Sixty-two patients were enrolled, 76 % completed the study, self-reported compliance was 98 %, and toxicities were minimal. At the end of treatment, the donepezil group performed significantly better than the control group on two parameters of memory-the Hopkins Verbal Learning Test -Revised (HVLT-R) Total Recall (p = 0.033) and HVLT-R Discrimination (p = 0.036). There were no significant differences on other cognitive variables or in subjective cognitive function or quality of life. Accrual to this feasibility trial was robust, retention was good, compliance was excellent, and toxicities were minimal. Randomized clinical trials in breast cancer survivors to improve cognitive dysfunction are feasible. A phase III trial testing the efficacy of donepezil is warranted given these pilot results.
引用
收藏
页码:176 / 184
页数:9
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