A descriptive study of persistent oxaliplatin-induced peripheral neuropathy in patients with colorectal cancer

被引:29
|
作者
Vatandoust, Sina [1 ]
Joshi, Rohit [1 ]
Pittman, Kenneth B. [2 ]
Esterman, Adrian [3 ,4 ]
Broadbridge, Vy [2 ]
Adams, Jacqueline [1 ]
Singhal, Nimit [1 ]
Yeend, Susan [2 ]
Price, Timothy Jay [5 ,6 ]
机构
[1] LyellMcEwin Hosp, Dept Med Oncol, Adelaide, SA, Australia
[2] Queen Elizabeth Hosp, Dept Med Oncol, Woodville, SA 5011, Australia
[3] Univ S Australia, Sansom Inst Hlth Serv Res, Adelaide, SA 5001, Australia
[4] Univ S Australia, Sch Nursing & Midwifery, Adelaide, SA 5001, Australia
[5] Queen Elizabeth Hosp, Woodville, SA 5011, Australia
[6] Univ Adelaide, Woodville, SA 5011, Australia
关键词
Oxaliplatin; Neurotoxicity syndromes; Colorectal neoplasms; Antineoplastic agents; Colonic neoplasms; Rectal neoplasms; Antineoplastic combined chemotherapy protocols; ROOT GANGLION NEURONS; III COLON-CANCER; SURGICAL ADJUVANT CHEMOTHERAPY; WEEKLY BOLUS FLUOROURACIL; STAGE-II; ALCOHOLIC NEUROPATHY; NEUROTOXICITY; LEUCOVORIN; PREVENTION; INFUSIONS;
D O I
10.1007/s00520-013-2004-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prolonged neurotoxicity after systemic chemotherapy has the potential to impact on quality of life. We explored the frequency of persistent peripheral neuropathy in patients who received oxaliplatin for colorectal cancer at two local centres. Questionnaires were sent to patients who completed treatment with oxaliplatin for colorectal cancer at least 20 months prior to entering the study. Neuropathy questions were adapted from the FACT/GOG-Ntx (V.4) questionnaire. Of the 56 eligible patients, 27 returned the questionnaire. Twenty-five patients (93 %) experienced neuropathic symptoms during their treatment; 11 had grade-2, and two had grade-3 symptoms. At the time of completing the questionnaire, 17 patients (63.0 %; 95%CI 43.9-79.4 %) were still symptomatic with 12 patients (44.4 %; 95%CI 26.8-63.3) having grade-2 or grade-3 symptoms and three patients (11.1 %; 95%CI 2.9-27.3) having grade-3 neuropathic symptoms. Participants who received more than 900 mg/m(2) oxaliplatin had a significantly higher risk of persistent grade-2 or grade-3 neuropathy (p = 0.031, RR = 8.3 95%CI = 1.2-57.4). There was a trend toward increased risk of persistent neuropathy of any grade among participants with a history of regular alcohol use (p = 0.051; RR = 1.7 95%CI 1.0-2.8). Persistent oxaliplatin-induced neuropathy is not as uncommon as previously suggested, and the rate of grade-2 and grade-3 symptoms could be considerably higher than previous reports.
引用
收藏
页码:513 / 518
页数:6
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