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甲磺酸伊马替尼作为一线治疗药物用于慢性期慢性髓性白血病的生活质量评估。

Assessment of quality of life with imatinib mesylate as first-line treatment in chronic phase-chronic myeloid leukemia.

机构信息

Department of Oncology, Allama Iqbal Medical College/Jinnah Hospital, Lahore, Pakistan.

出版信息

Leuk Lymphoma. 2011 Jun;52(6):1017-23. doi: 10.3109/10428194.2011.560310. Epub 2011 May 3.

Abstract

Imatinib mesylate (IM) is a first-line treatment of chronic phase-chronic myeloid leukemia (CP-CML). The primary objective of this study was to assess the quality of life (QOL) in patients with CP-CML treated with IM. Ninety patients with newly diagnosed CP-CML were assessed for QOL with first-line IM. Patients completed the cancer-specific FACT-BRM questionnaire (functional assessment of cancer therapy-biologic response modifiers) at baseline and at 3 and 6 months. FACT-BRM consists of subscales including physical well-being (PWB), social and family well-being (SFWB), emotional well-being (EWB), functional well-being (FWB), BRM-physical, and BRM-mental. The primary endpoint was the Trial Outcome Index (TOI), created as a measure of physical function and well-being. An increase of ≥5 from baseline was considered to be a clinically significant improvement. The mean TOI score increased from 75.5 at baseline to 85.2 (p<0.0001) at 6 months, representing a healthy QOL. When comparing the individual TOI subscales, there was a mean increase of 16.4 in the daily functioning and well-being score, and a mean decrease of 6.2, 4.9, and 16.1 was noted in fatigue, emotional/cognitive dysfunction, and side-effects scores at 6 months, respectively. Improvement was not affected by age, sex, or Sokal score. With prolonged treatment, IM results in a higher physical well-being, less fatigue and emotional and cognitive dysfunction, and very few side-effects.

摘要

甲磺酸伊马替尼(IM)是慢性期慢性髓性白血病(CP-CML)的一线治疗药物。本研究的主要目的是评估接受 IM 治疗的 CP-CML 患者的生活质量(QOL)。对 90 例新诊断为 CP-CML 的患者进行了一线 IM 治疗的 QOL 评估。患者在基线和 3 个月和 6 个月时完成了癌症特异性 FACT-BRM 问卷(癌症治疗功能评估-生物反应调节剂)。FACT-BRM 包括身体状况(PWB)、社会和家庭状况(SFWB)、情感状况(EWB)、功能状况(FWB)、BRM-身体和 BRM-心理等子量表。主要终点是试验结局指数(TOI),作为身体功能和健康状况的衡量标准。与基线相比,增加≥5 被认为是临床显著改善。TOI 评分从基线时的 75.5 增加到 6 个月时的 85.2(p<0.0001),代表了健康的 QOL。当比较个体 TOI 子量表时,日常生活功能和健康状况评分平均增加了 16.4,疲劳、情绪/认知功能障碍和副作用评分分别平均下降了 6.2、4.9 和 16.1。改善不受年龄、性别或 Sokal 评分的影响。随着治疗时间的延长,IM 可提高身体舒适度、减轻疲劳、情绪和认知功能障碍,且副作用很少。

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