Rapp Stephen R, Case L Doug, Peiffer Ann, Naughton Michelle M, Chan Michael D, Stieber Volker W, Moore Dennis F, Falchuk Steven C, Piephoff James V, Edenfield William J, Giguere Jeffrey K, Loghin Monica E, Shaw Edward G
Stephen R. Rapp, L. Doug Case, Ann Peiffer, Michelle M. Naughton, Michael D. Chan, and Edward G. Shaw, Wake Forest School of Medicine and Wake Forest Community Clinical Oncology Program Research Base; Volker W. Stieber, Novant Health System, Winston-Salem, NC; Dennis F. Moore Jr, Wichita Community Clinical Oncology Program, Wichita, KS; Steven C. Falchuk, Christiana Care Health Services, Newark, DE; James V. Piephoff, Mercy Hospital, St Louis, MO; William J. Edenfield and Jeffrey K. Giguere, Cancer Center of Carolinas, Greenville, SC; and Monica E. Loghin, University of Texas MD Anderson Cancer Center, Houston, TX.
J Clin Oncol. 2015 May 20;33(15):1653-9. doi: 10.1200/JCO.2014.58.4508. Epub 2015 Apr 20.
PURPOSE: Neurotoxic effects of brain irradiation include cognitive impairment in 50% to 90% of patients. Prior studies have suggested that donepezil, a neurotransmitter modulator, may improve cognitive function. PATIENTS AND METHODS: A total of 198 adult brain tumor survivors ≥ 6 months after partial- or whole-brain irradiation were randomly assigned to receive a single daily dose (5 mg for 6 weeks, 10 mg for 18 weeks) of donepezil or placebo. A cognitive test battery assessing memory, attention, language, visuomotor, verbal fluency, and executive functions was administered before random assignment and at 12 and 24 weeks. A cognitive composite score (primary outcome) and individual cognitive domains were evaluated. RESULTS: Of this mostly middle-age, married, non-Hispanic white sample, 66% had primary brain tumors, 27% had brain metastases, and 8% underwent prophylactic cranial irradiation. After 24 weeks of treatment, the composite scores did not differ significantly between groups (P = .48); however, significant differences favoring donepezil were observed for memory (recognition, P = .027; discrimination, P = .007) and motor speed and dexterity (P = .016). Significant interactions between pretreatment cognitive function and treatment were found for cognitive composite (P = .01), immediate recall (P = .05), delayed recall (P = .004), attention (P = .01), visuomotor skills (P = .02), and motor speed and dexterity (P < .001), with the benefits of donepezil greater for those who were more cognitively impaired before study treatment. CONCLUSION: Treatment with donepezil did not significantly improve the overall composite score, but it did result in modest improvements in several cognitive functions, especially among patients with greater pretreatment impairments.
目的:脑部放疗的神经毒性作用包括50%至90%的患者出现认知障碍。先前的研究表明,作为一种神经递质调节剂的多奈哌齐可能改善认知功能。 患者与方法:共有198名在接受部分或全脑放疗后至少6个月的成人大脑肿瘤幸存者被随机分配,接受每日一次剂量(6周5毫克,18周10毫克)的多奈哌齐或安慰剂治疗。在随机分组前以及第12周和第24周时,进行了一组评估记忆、注意力、语言、视觉运动、言语流畅性和执行功能的认知测试。评估了认知综合评分(主要结局)和各个认知领域。 结果:在这个主要为中年、已婚、非西班牙裔白人的样本中,66%患有原发性脑肿瘤,27%患有脑转移瘤,8%接受了预防性颅脑照射。治疗24周后,两组之间的综合评分无显著差异(P = 0.48);然而,在记忆(识别,P = 0.027;辨别,P = 0.007)以及运动速度和灵活性方面(P = 0.016),观察到多奈哌齐组有显著优势。在认知综合评分(P = 0.01)、即时回忆(P = 0.05)、延迟回忆(P = 0.004)、注意力(P = 0.01)、视觉运动技能(P = 0.02)以及运动速度和灵活性(P < 0.001)方面,发现治疗前认知功能与治疗之间存在显著交互作用,对于研究治疗前认知障碍程度较重的患者,多奈哌齐的益处更大。 结论:多奈哌齐治疗并未显著改善总体综合评分,但确实使几种认知功能有适度改善,尤其是在治疗前损伤较重的患者中。
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