Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Department of Oncology, Mayo Clinic, Rochester, Minnesota, USA.
J Neurol Neurosurg Psychiatry. 2018 Jun;89(6):636-641. doi: 10.1136/jnnp-2017-317215. Epub 2018 Feb 8.
To assess disease burden of chemotherapy-induced peripheral neuropathy (CIPN), which is a common dose-limiting side effect of neurotoxic chemotherapy. Late effects of CIPN may increase with improved cancer survival.
Olmsted County, Minnesota residents receiving neurotoxic chemotherapy were identified and CIPN was ascertained via text searches of polyneuropathy symptoms in the medical record. Clinical records were queried to collect data on baseline characteristics, risk factors, signs and symptoms of CIPN, medications, impairments and International Classification of Diseases, Ninth Revision (ICD-9) diagnostic codes for all subjects.
A total of 509 individuals with incident exposure to an inclusive list of neurotoxic chemotherapy agents between 2006 and 2008 were identified. 268 (52.7%) of these individuals were determined to have CIPN. The median time from incident exposure to first documented symptoms was 71 days. Patients with CIPN received a neuropathy ICD-9 diagnosis in only 37 instances (13.8%). Pain symptoms and use of pain medications were observed more often in patients with CIPN. Five-year survival was greater in those with CIPN (55.2%) versus those without (36.1%). Those with CIPN surviving greater than 5 years (n=145) continued to have substantial impairments and were more likely to be prescribed opioids than those without CIPN (OR 2.0, 1.06-3.69).
Results from our population-based study are consistent with previous reports of high incidence of CIPN in the first 2 years following incident exposure to neurotoxic chemotherapeutic agents, and its association with significant pain symptomatology and accompanied long-term opioid use. Increased survival following exposure to neurotoxic chemotherapy and its long-term disease burden necessitates further study among survivors.
评估化疗引起的周围神经病(CIPN)的疾病负担,这是神经毒性化疗的常见剂量限制副作用。CIPN 的迟发效应可能随着癌症生存率的提高而增加。
在明尼苏达州奥姆斯特德县,确定接受神经毒性化疗的居民,并通过病历中多发性神经病症状的文本搜索来确定 CIPN。临床记录被查询,以收集所有受试者的基线特征、危险因素、CIPN 的体征和症状、药物、损伤以及所有受试者的国际疾病分类,第 9 版(ICD-9)诊断代码的数据。
共确定了 509 名在 2006 年至 2008 年间接触包括神经毒性化疗药物在内的所有药物的个体发生暴露。其中 268 名(52.7%)被确定患有 CIPN。从发病暴露到首次记录症状的中位时间为 71 天。患有 CIPN 的患者仅在 37 例(13.8%)中被诊断为神经病 ICD-9。疼痛症状和使用疼痛药物在 CIPN 患者中更为常见。患有 CIPN 的患者的五年生存率高于无 CIPN 的患者(55.2%对 36.1%)。在 CIPN 存活超过 5 年的患者(n=145)中,与无 CIPN 的患者相比,他们继续存在严重的损伤,并且更有可能被开阿片类药物(OR 2.0,1.06-3.69)。
我们的基于人群的研究结果与先前关于神经毒性化疗药物暴露后 2 年内 CIPN 发生率高的报告一致,以及其与显著疼痛症状学的相关性,并伴有长期阿片类药物使用。接触神经毒性化疗后的生存率提高及其长期疾病负担需要在幸存者中进一步研究。