Oxaliplatin- and docetaxel-induced polyneuropathy: clinical and neurophysiological characteristics

被引:34
作者
Bennedsgaard, Kristine [1 ]
Ventzel, Lise [1 ,2 ]
Andersen, Niels T. [3 ]
Themistocleous, Andreas C. [4 ,5 ]
Bennett, David L. [4 ]
Jensen, Troels S. [1 ,6 ]
Tankisi, Hatice [7 ]
Finnerup, Nanna B. [1 ,6 ]
机构
[1] Aarhus Univ, Danish Pain Res Ctr, Dept Clin Med, Palle Juul Jensens Blvd 1, DK-8200 Aarhus N, Denmark
[2] Aarhus Univ Hosp, Dept Oncol, Aarhus, Denmark
[3] Aarhus Univ, Dept Publ Hlth, Biostat, Aarhus, Denmark
[4] Univ Oxford, Nuffield Dept Clin Neurosci, Oxford, England
[5] Univ Witwatersrand, Fac Hlth Sci, Sch Physiol, Brain Funct Res Grp, Johannesburg, South Africa
[6] Aarhus Univ Hosp, Dept Neurol, Aarhus, Denmark
[7] Aarhus Univ Hosp, Dept Neurophysiol, Aarhus, Denmark
基金
欧盟地平线“2020”;
关键词
assessment tools; chemotherapy; corneal confocal microscopy; large fiber neuropathy; motor unit number estimation; nerve conduction study; neuropathic pain; neuropathy; pain; small fiber neuropathy; INDUCED PERIPHERAL NEUROPATHY; QUALITY-OF-LIFE; CORNEAL CONFOCAL MICROSCOPY; COLORECTAL-CANCER; DIAGNOSTIC-CRITERIA; CHEMOTHERAPY; PAIN; SEVERITY; QUESTIONNAIRE; VALIDATION;
D O I
10.1111/jns.12413
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The aim of this study was to evaluate the presence and characterization of chemotherapy-induced neuropathy (CIPN) and neuropathic pain 5 years after adjuvant chemotherapy with docetaxel or oxaliplatin. Patients from an ongoing prospective study, who had received adjuvant chemotherapy with docetaxel or oxaliplatin in 2011 to 2012 were invited to participate. The patients underwent a thorough examination with interview, neurological examination, questionnaires, assessment tools, nerve conduction studies (NCS), quantitative sensory testing, MScan motor unit number estimation (MUNE), and corneal confocal microscopy (CCM). Patients were divided into no, possible, probable, and confirmed CIPN. Out of the 132 eligible patients, 63 agreed to participate: 28 had received docetaxel and 35 had received oxaliplatin. Forty-one percent had confirmed CIPN, 34% possible or probable CIPN, and 22% did not have CIPN. The CIPN was characterized mainly by sensory nerve fiber loss, with a more pronounced large fiber than small fiber loss but also some motor fiber loss identified on NCS and MUNE. In general, patients had mild neuropathy with relatively low scores on assessment tools and no association with mood and quality of life. CCM was not useful as a diagnostic tool. Of the patients with probable or confirmed CIPN, 30% experienced pain, which was most often mild, but still interfered moderately with daily life in 20% to 25% and was associated with lower quality of life. In conclusion CIPN was confirmed in 41% 5 years after chemotherapy. The neuropathy was generally mild, but in patients with neuropathic pain it was associated with lower quality of life.
引用
收藏
页码:377 / 387
页数:11
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