Clinical and electrophysiological features of peripheral neuropathy induced by administration of cisplatin plus paclitaxel-based chemotherapy

被引:46
作者
Argyriou, A. A.
Polychronopoulos, P.
Koutras, A.
Xiros, N.
Petsas, T.
Argyriou, K.
Kalofonos, H. P.
Chroni, E.
机构
[1] Univ Patras, Sch Med, Dept Neurol, Clin Neurophysiol Lab, Rion, Greece
[2] Univ Patras, Sch Med, Dept Med, Div Oncol, Rion, Greece
关键词
cisplatin plus paclitaxel; peripheral neuropathy; incidence; severity; evolution;
D O I
10.1111/j.1365-2354.2006.00718.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The current prospective study sought to trace the incidence and severity of cisplatin plus paclitaxel (DDP+P)-induced neuropathy and to determine its clinical and electrophysiological pattern. Furthermore, it was attempted to describe its evolution by following up the course of peripheral neuropathy (PN) during chemotherapy as well as 3 months after its discontinuation. Thirteen adult patients scheduled to be treated with six courses of cumulative DDP+P-based regimens for a non-myeloid malignancy participated in this study. These patients were clinically and electrophysiologically monitored at baseline, during chemotherapy and 3 months after its discontinuation. The severity of PN was summarized by means of a modified PN score. Evidence of PN was disclosed in nine of the 13 patients (69.2%). The mean PN score for patients that manifested some grade of PN was 17.3 +/- 6.1 (range 9-28). All longitudinal comparisons concerning the motor conduction velocities (MCV) variables failed to reach significance. By contrast, comparisons of the mean changes at baseline and each of the follow-up studies revealed a significant decrease in all sensory action potentials examined. The follow-up evaluation performed 3 months after the discontinuation of chemotherapy showed that the DDP+P-induced neuropathy persists and progresses over time. Our results indicate that the majority of patients treated with a DDP+P-based regimen at full dose intensities would manifest an axonal, predominately sensory PN, of mild to moderate severity, which would persist for several months after the discontinuation of chemotherapy.
引用
收藏
页码:231 / 237
页数:7
相关论文
共 33 条
  • [1] Paclitaxel and cisplatin in patients with recurrent and metastatic head and neck squamous cell carcinoma
    Adamo, V
    Ferraro, G
    Pergolizzi, S
    Sergi, C
    Laudani, A
    Settineri, N
    Alafaci, E
    Scimone, A
    Spano, F
    Spitaleri, G
    [J]. ORAL ONCOLOGY, 2004, 40 (05) : 525 - 531
  • [2] [Anonymous], ELECTRODIAGNOSIS DIS
  • [3] Vitamin E for prophylaxis against chemotherapy-induced neuropathy - A randomized controlled trial
    Argyriou, AA
    Chroni, E
    Koutras, A
    Ellul, J
    Papapetropoulos, S
    Katsoulas, G
    Iconomou, G
    Kalofonos, HP
    [J]. NEUROLOGY, 2005, 64 (01) : 26 - 31
  • [4] Neurological monitoring of neurotoxicity induced by paclitaxel/cisplatin chemotherapy
    Berger, T
    Malayeri, R
    Doppelbauer, A
    Krajnik, G
    Huber, H
    Auff, E
    Pirker, R
    [J]. EUROPEAN JOURNAL OF CANCER, 1997, 33 (09) : 1393 - 1399
  • [5] Neurotoxicity and ototoxicity of cisplatin plus paclitaxel in comparison to cisplatin plus cyclophosphamide in patients with epithelial ovarian cancer
    Cavaletti, G
    Bogliun, G
    Crespi, V
    Marzorati, L
    Zincone, A
    Marzola, M
    Rota, S
    Galli, A
    Tredici, P
    Tredici, G
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (01) : 199 - 206
  • [6] CAVALETTI G, 1995, CANCER, V75, P1141, DOI 10.1002/1097-0142(19950301)75:5<1141::AID-CNCR2820750514>3.0.CO
  • [7] 2-U
  • [8] PERIPHERAL NEUROPATHY FROM TAXOL AND CISPLATIN COMBINATION CHEMOTHERAPY - CLINICAL AND ELECTROPHYSIOLOGICAL STUDIES
    CHAUDHRY, V
    ROWINSKY, EK
    SARTORIUS, SE
    DONEHOWER, RC
    CORNBLATH, DR
    [J]. ANNALS OF NEUROLOGY, 1994, 35 (03) : 304 - 311
  • [9] Davidson NG, 1996, SEMIN ONCOL, V23, P6
  • [10] Paclitaxel and cisplatin in advanced or recurrent carcinoma of the endometrium: Long-term results of a phase II multicenter study
    Dimopoulos, MA
    Papadimitriou, CA
    Georgoulias, V
    Moulopoulos, LA
    Aravantinos, G
    Gika, D
    Karpathios, S
    Stamatelopoulos, S
    [J]. GYNECOLOGIC ONCOLOGY, 2000, 78 (01) : 52 - 57