Advanced age and liability to oxaliplatin-induced peripheral neuropathy: post hoc analysis of a prospective study
Article first published online: 17 DEC 2012
© 2012 The Author(s) European Journal of Neurology © 2012 EFNS
European Journal of Neurology
Volume 20, Issue 5, pages 788–794, May 2013
How to Cite
Argyriou, A. A., Briani, C., Cavaletti, G., Bruna, J., Alberti, P., Velasco, R., Lonardi, S., Cortinovis, D., Cazzaniga, M., Campagnolo, M., Santos, C. and Kalofonos, H. P. (2013), Advanced age and liability to oxaliplatin-induced peripheral neuropathy: post hoc analysis of a prospective study. European Journal of Neurology, 20: 788–794. doi: 10.1111/ene.12061
- Issue published online: 11 APR 2013
- Article first published online: 17 DEC 2012
- Manuscript Accepted: 1 NOV 2012
- Manuscript Received: 5 JUL 2012
- Instituto de Salud Carlos III. Grant Number: PI070493
Background and purpose
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.