Mortimer Joanne E, Waliany Sarah, Dieli-Conwright Christina M, Patel Sunita K, Hurria Arti, Chao Joseph, Tiep Brian, Behrendt Carolyn E
Department of Medical Oncology, City of Hope Comprehensive Cancer Center, Duarte, California.
Division of Biokinesiology and Physical Therapy, University of Southern California, Los Angeles, California.
Cancer. 2017 May 15;123(10):1810-1816. doi: 10.1002/cncr.30426. Epub 2017 Jan 6.
Objective, treatment-independent markers of cancer-related fatigue are needed to advance clinical trials. In the current study, the authors evaluated physical, neurocognitive, and serologic markers for correlation with self-reported fatigue before and after (neo)adjuvant chemotherapy for patients with early-stage breast cancer.
Women with AJCC TNM Stage I-III breast cancer consented to assessment before and after the completion of 4 cycles of dose-dense doxorubicin and cyclophosphamide. Assessment included self-reported fatigue (using the Brief Fatigue Inventory), depression (using the Center for Epidemiologic Studies-Depression Scale [CES-D]), Pittsburgh Sleep Quality Index, and 28 objective measures (grip strength in dominant and nondominant hands, 6-minute walk, daily total energy expenditure, 14 neurocognitive tests, and 10 serologic markers). Generalized linear regression models of fatigue were constructed (1 model per marker), and adjusted for depression, timing before/after chemotherapy, menopausal status, obesity, and educational level. P values were adjusted to control the False Discovery Rate.
Of 28 subjects, 3 withdrew without completing baseline assessments. Prechemotherapy and postchemotherapy data were available for the evaluation of physical measures (25 subjects aged 50.6 ± 9.5 years), neurocognitive tests (22 subjects), and serologic markers (10 subjects). On covariate-adjusted analysis, interleukin (IL)-12 was found to be associated with fatigue at both assessments (P<.01). Serum eotaxin (P < .01), IL-1RA (P < .01), monocyte chemoattractant protein 1 (MCP-1) (P<.01), and performance on 2 neurocognitive (Trail Making) tests (P<.01 and P = .02, respectively) were found to be inversely associated with fatigue before chemotherapy but not afterward, whereas daily energy expenditure, serum MCP-1, and serum macrophage inflammatory protein 1a (MIP-1a) were found to be associated with fatigue after receipt of chemotherapy but not before (P<.01 for each). The association between energy expenditure and fatigue was detectable only if an actively athletic subject with outlier values of energy expenditure was excluded.
Serum IL-12 merits confirmatory testing as an objective, treatment-independent measure of fatigue in patients with early-stage breast cancer. Cancer 2017;123:1810-1816. © 2017 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
推进临床试验需要与癌症相关疲劳无关的客观治疗指标。在本研究中,作者评估了身体、神经认知和血清学指标与早期乳腺癌患者(新)辅助化疗前后自我报告的疲劳之间的相关性。
美国癌症联合委员会(AJCC)TNM分期为I-III期的乳腺癌女性患者同意在完成4个周期的剂量密集型阿霉素和环磷酰胺化疗前后接受评估。评估内容包括自我报告的疲劳(使用简明疲劳量表)、抑郁(使用流行病学研究中心抑郁量表[CES-D])、匹兹堡睡眠质量指数以及28项客观指标(优势手和非优势手的握力、6分钟步行距离、每日总能量消耗、14项神经认知测试和10项血清学指标)。构建了疲劳的广义线性回归模型(每个指标1个模型),并对抑郁、化疗前后时间、绝经状态、肥胖和教育水平进行了调整。对P值进行了调整以控制假发现率。
28名受试者中,3人未完成基线评估即退出。可获得化疗前和化疗后的身体指标(25名年龄50.6±9.5岁的受试者)、神经认知测试(22名受试者)和血清学指标(10名受试者)数据用于评估。在协变量调整分析中,发现白细胞介素(IL)-12在两次评估时均与疲劳相关(P<.01)。血清嗜酸性粒细胞趋化因子(P<.01)、IL-1受体拮抗剂(IL-1RA)(P<.01)、单核细胞趋化蛋白1(MCP-1)(P<.01)以及2项神经认知(连线)测试的表现(分别为P<.01和P=.02)在化疗前与疲劳呈负相关,但化疗后无此相关性,而每日能量消耗、血清MCP-1和血清巨噬细胞炎性蛋白1α(MIP-1α)在化疗后与疲劳相关,但化疗前无此相关性(每项P<.01)。仅当排除一名能量消耗值异常的积极运动受试者时,才能检测到能量消耗与疲劳之间的关联。
血清IL-12作为早期乳腺癌患者疲劳客观、与治疗无关的指标,值得进一步验证性检测。《癌症》2017年;123:1810 - 1816。©2017作者。《癌症》由威利期刊公司代表美国癌症协会出版。这是一篇根据知识共享署名 - 非商业性使用 - 禁止演绎许可条款的开放获取文章,允许在任何媒介中使用和传播,前提是正确引用原始作品,使用为非商业性且不进行修改或改编。