Department of Oncology, Cumming School of Medicine, University of Calgary, Tom Baker Cancer Centre, 1331 29 St NW, Calgary, Alberta, T2N 4N2, Canada.
Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
BMC Cancer. 2019 Feb 14;19(1):150. doi: 10.1186/s12885-019-5349-2.
Cognitive impairment is commonly reported in patients receiving chemotherapy, but the acuity of onset is not known. This study utilized the psychomotor vigilance test (PVT) and trail-making test B (TMT-B) to assess cognitive impairment immediately post-chemotherapy.
Patients aged 18-80 years receiving first-line intravenous chemotherapy for any stage of breast or colorectal cancer were eligible. Patient symptoms, peripheral neuropathy and Stanford Sleepiness Scale were assessed. A five-minute PVT and TMT-B were completed on a tablet computer pre-chemotherapy and immediately post-chemotherapy. Using a mixed linear regression model, changes in reciprocal transformed PVT reaction time (mean 1/RT) were assessed. A priori, an increase in median PVT reaction times by > 20 ms (approximating PVT changes with blood alcohol concentrations of 0.04-0.05 g%) was considered clinically relevant.
One hundred forty-two cancer patients (73 breast, 69 colorectal, median age 55.5 years) were tested. Post-chemotherapy, mean 1/RT values were significantly slowed compared to pre-chemotherapy baseline (p = 0.01). This corresponded to a median PVT reaction time slowed by an average of 12.4 ms. Changes in PVT reaction times were not correlated with age, sex, cancer type, treatment setting, or use of supportive medications. Median post-chemotherapy PVT reaction time slowed by an average of 22.5 ms in breast cancer patients and by 1.6 ms in colorectal cancer patients. Post-chemotherapy median PVT times slowed by > 20 ms in 57 patients (40.1%). Exploratory analyses found no statistically significant association between the primary outcome and self-reported anxiety, fatigue or depression. TMT-B completion speed improved significantly post-chemotherapy (p = 0.03), likely due to test-retest phenomenon.
PVT reaction time slowed significantly immediately post-chemotherapy compared to a pre-chemotherapy baseline, and levels of impairment similar to effects of alcohol consumption in other studies was seen in 40% of patients. Further studies assessing functional impact of cognitive impairment on patients immediately after chemotherapy are warranted.
接受化疗的患者常报告认知障碍,但发病的急缓程度尚不清楚。本研究利用精神运动警觉测试(PVT)和连线测试 B(TMT-B)来评估化疗后即刻的认知障碍。
符合条件的患者为 18-80 岁,正在接受一线静脉化疗,无论乳腺癌或结直肠癌处于哪一期。评估患者的症状、周围神经病变和斯坦福嗜睡量表。在平板电脑上进行 5 分钟的 PVT 和 TMT-B 测试,分别在化疗前和化疗后即刻完成。采用混合线性回归模型评估倒数转化的 PVT 反应时间(平均 1/RT)的变化。依据先前研究,PVT 反应时间中位数增加>20 毫秒(近似于血液酒精浓度为 0.04-0.05g%时的 PVT 变化)被认为具有临床意义。
共对 142 名癌症患者(73 名乳腺癌患者,69 名结直肠癌患者,中位年龄 55.5 岁)进行了测试。与化疗前基线相比,化疗后平均 1/RT 值显著减慢(p=0.01)。这相当于 PVT 反应时间的中位数平均减慢 12.4 毫秒。PVT 反应时间的变化与年龄、性别、癌症类型、治疗环境或支持性药物的使用无关。乳腺癌患者的平均 PVT 反应时间减慢了 22.5 毫秒,结直肠癌患者减慢了 1.6 毫秒。化疗后,57 名患者(40.1%)的 PVT 中位数减慢超过 20 毫秒。探索性分析发现,主要结局与自我报告的焦虑、疲劳或抑郁之间无统计学显著关联。TMT-B 完成速度在化疗后显著提高(p=0.03),可能是由于测试-重测现象。
与化疗前基线相比,PVT 反应时间在化疗后即刻明显减慢,40%的患者出现了与其他研究中酒精作用相似的损害程度。需要进一步研究评估化疗后即刻认知障碍对患者的功能影响。