Longitudinal assessment of oxaliplatin-induced neuropathy

被引:87
作者
Burakgazi, A. Z. [1 ]
Messersmith, W. [3 ]
Vaidya, D. [4 ]
Hauer, P. [1 ]
Hoke, A. [2 ]
Polydefkis, M. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21231 USA
[4] Johns Hopkins Univ, Sch Med, Dept Internal Med, Baltimore, MD 21231 USA
关键词
INDUCED PERIPHERAL NEUROTOXICITY; ADVANCED COLORECTAL-CANCER; NERVE-FIBER DENSITY; PHASE-II; CHEMOTHERAPY; FLUOROURACIL; LEUCOVORIN; CARCINOMA; RESISTANT; TRIAL;
D O I
10.1212/WNL.0b013e31822cfc59
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Objectives: To characterize the natural history of oxaliplatin-associated neuropathy (ON) and determine whether intraepidermal nerve fiber density (IENFD) is a sensitive measure of neuropathy progression. In addition, we sought to assess the potential of ON as a neuroprotection model and gain insight into the relationship between axon loss and neuropathic symptoms. Methods: Eight subjects receiving oxaliplatin for advanced colorectal cancer were prospectively followed prior to starting chemotherapy and at 30, 90, 180, and 360 days (180 days after completing treatment). Electrophysiology, punch biopsies, symptom assessment, and examinations with calculation of a reduced total neuropathy score (rTNS) were performed at each time point. Changes over time were assessed through Poisson regression for IENFD and a mixed effects model for rTNS and electrophysiology measures. Results: The distal leg IENFD, rTNS, peroneal, and sural amplitudes were all significantly reduced over time, while conduction velocity (peroneal and sural) and distal thigh IENFD were not. Measures of axon loss continued to worsen following discontinuation of oxaliplatin. Five of 8 subjects reported prominent symptoms associated with oxaliplatin administration. Conclusions: This study demonstrates that oxaliplatin is associated with mild, sensory, and motor axon loss that may not be reversible. Axonal loss was detected by electrophysiology, rTNS, and distal leg IENFD. Several subjects reported prominent sensory symptoms that were not associated with axon loss, and that may or may not represent neuropathy. ON is an attractive paradigm for neuroprotection studies and the distal leg IENFD is an objective measure that requires minimal subject participation or study site expertise. Neurology (R) 2011;77:980-986
引用
收藏
页码:980 / 986
页数:7
相关论文
共 22 条
[1]
Multicenter phase II study of bimonthly high-dose leucovorin, fluorouracil infusion, and oxaliplatin for metastatic colorectal cancer resistant to the same leucovorin and fluorouracil regimen [J].
André, T ;
Bensmaine, MA ;
Louvet, C ;
François, E ;
Lucas, V ;
Desseigne, F ;
Beerblock, K ;
Bouché, O ;
Carola, E ;
Merrouche, Y ;
Morvan, F ;
Dupon-André, G ;
de Gramont, A .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (11) :3560-3568
[2]
Phase II trial of oxaliplatin as first-line chemotherapy in metastatic colorectal cancer patients [J].
Bécouarn, Y ;
Ychou, M ;
Ducreux, M ;
Borel, C ;
Bertheault-Cvitkovic, F ;
Seitz, JF ;
Nasca, S ;
Nguyen, TD ;
Paillot, B ;
Raoul, JL ;
Duffour, J ;
Fandi, A ;
Dupont-André, G ;
Rougier, P .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (08) :2739-2744
[3]
Multi-center assessment of the Total Neuropathy Score for chemotherapy-induced peripheral neurotoxicity [J].
Cavaletti, G ;
Jann, S ;
Pace, A ;
Plasmati, R ;
Siciliano, G ;
Briani, C ;
Cocito, D ;
Padua, L ;
Ghiglione, E ;
Manicone, M ;
Giussani, G .
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2006, 11 (02) :135-141
[4]
Grading of chemotherapy-induced peripheral neurotoxicity using the Total Neuropathy Scale [J].
Cavaletti, G ;
Bogliun, G ;
Marzorati, L ;
Zincone, A ;
Piatti, M ;
Colombo, N ;
Parma, G ;
Lissoni, A ;
Fei, F ;
Cundari, S ;
Zanna, C .
NEUROLOGY, 2003, 61 (09) :1297-1300
[5]
Oxaliplatin-associated neuropathy: A review [J].
Cersosimo, RJ .
ANNALS OF PHARMACOTHERAPY, 2005, 39 (01) :128-135
[6]
PERIPHERAL NEUROPATHY FROM TAXOL AND CISPLATIN COMBINATION CHEMOTHERAPY - CLINICAL AND ELECTROPHYSIOLOGICAL STUDIES [J].
CHAUDHRY, V ;
ROWINSKY, EK ;
SARTORIUS, SE ;
DONEHOWER, RC ;
CORNBLATH, DR .
ANNALS OF NEUROLOGY, 1994, 35 (03) :304-311
[7]
A prospective study of suramin-induced peripheral neuropathy [J].
Chaudhry, V ;
Eisenberger, MA ;
Sinibaldi, VJ ;
Sheikh, K ;
Griffin, JW ;
Cornblath, DR .
BRAIN, 1996, 119 :2039-2052
[8]
Can Chemotherapy Be Discontinued in Unresectable Metastatic Colorectal Cancer? The GERCOR OPTIMOX2 Study [J].
Chibaudel, Benoist ;
Maindrault-Goebel, Frederique ;
Lledo, Gerard ;
Mineur, Laurent ;
Andre, Thierry ;
Bennamoun, Mostepha ;
Mabro, May ;
Artru, Pascal ;
Carola, Elisabeth ;
Flesch, Michel ;
Dupuis, Olivier ;
Colin, Philippe ;
Larsen, Annette K. ;
Afchain, Pauline ;
Tournigand, Christophe ;
Louvet, Christophe ;
de Gramont, Aimery .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (34) :5727-5733
[9]
Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer [J].
de Gramont, A ;
Figer, A ;
Seymour, M ;
Homerin, M ;
Hmissi, A ;
Cassidy, J ;
Boni, C ;
Cortes-Funes, H ;
Cervantes, A ;
Freyer, G ;
Papamichael, D ;
Le Bail, N ;
Louvet, C ;
Hendler, D ;
de Braud, F ;
Wilson, C ;
Morvan, F ;
Bonetti, A .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (16) :2938-2947
[10]
Oxaliplatin as single agent in previously untreated colorectal carcinoma patients: A phase II multicentric study [J].
Diaz-Rubio, E ;
Sastre, J ;
Zaniboni, A ;
Labianca, R ;
Cortes-Funes, H ;
de Braud, F ;
Boni, C ;
Benavides, M ;
Dallavalle, G ;
Homerin, M .
ANNALS OF ONCOLOGY, 1998, 9 (01) :105-108