Department of Neurology, Saint Andrew's State General Hospital of Patras, Patras, Greece.
Eur J Neurol. 2013 May;20(5):788-94. doi: 10.1111/ene.12061. Epub 2012 Dec 17.
The aim of this post hoc analysis of data extracted from a prospective, multicenter study is to test in a large homogenous population of chemotherapy-naïve patients with colorectal cancer (CRC) treated with oxaliplatin (OXA)-based chemotherapy whether advanced age increases the risk of developing OXA-induced peripheral neuropathy (OXAIPN).
One-hundred and forty-five patients with CRC, without other significant co-morbidities predisposing to peripheral neuropathy, were divided according to their age into two groups: patients aged between 50 and 68 years (group I, n = 75); and patients aged ≥ 69 years (group II, n = 70). Patients were prospectively monitored at baseline and followed-up during chemotherapy using the motor and neurosensory National Cancer Institute Common Toxicity criteria, the clinical version of the Total Neuropathy Score and neurophysiology. The incidence and severity of both the acute and cumulative OXAIPN was thoroughly determined and then compared between age groups.
No statistically significant difference was observed in the incidence of both the acute (n = 64/75 vs. 56/70; P = 0.510) and cumulative OXAIPN (n = 51/75 vs. 49/70; P = 0.858) between age groups. The severity of OXAIPN was also similar between age groups. In line with the clinical data, the neurophysiological results between age groups were also comparable.
The results of this study indicate that advanced age does not seem to represent a significant risk factor of OXAIPN in patients with CRC without any other significant co-morbidities.
本研究旨在对一项前瞻性、多中心研究中提取的数据进行事后分析,以检验在接受奥沙利铂(OXA)为基础化疗的、无其他显著合并症导致周围神经病变风险的结直肠癌(CRC)化疗初治患者这一大同质人群中,高龄是否会增加发生 OXA 诱导的周围神经病变(OXAIPN)的风险。
145 例无其他显著合并症导致周围神经病变风险的 CRC 患者,根据年龄分为两组:50-68 岁患者(I 组,n = 75);≥69 岁患者(II 组,n = 70)。患者在基线时接受前瞻性监测,并在化疗期间使用国家癌症研究所(NCI)通用毒性标准、总神经病变评分(Total Neuropathy Score)的临床版和神经生理学进行随访。详细确定急性和累积 OXAIPN 的发生率和严重程度,并在两组之间进行比较。
两组急性(n = 64/75 比 n = 56/70;P = 0.510)和累积 OXAIPN(n = 51/75 比 n = 49/70;P = 0.858)的发生率均无统计学差异。两组间 OXAIPN 的严重程度也相似。与临床数据一致,两组间的神经生理学结果也相当。
本研究结果表明,在无其他显著合并症的 CRC 患者中,高龄似乎不是 OXAIPN 的显著危险因素。