Are we mis-estimating chemotherapy-induced peripheral neuropathy? Analysis of assessment methodologies from a prospective, multinational, longitudinal cohort study of patients receiving neurotoxic chemotherapy

Are we mis-estimating chemotherapy-induced peripheral neuropathy? Analysis of assessment methodologies from a prospective, multinational, longitudinal cohort study of patients receiving neurotoxic chemotherapy
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DOI:
10.1186/s12885-019-5302-4
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发表时间:
2019-02-08
期刊:
影响因子:
3.8
通讯作者:
Sundar, Raghav
Sundar, Raghav
中科院分区:
医学2区
文献类型:
--
作者:
Molassiotis, Alex;Cheng, Hui Lin;Sundar, Raghav

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背景关于化疗引起的周围神经病变(CIPN)的患病率和评估,文献中存在不一致。本研究探讨了CIPN的自然历史和它的特点,在接受紫杉烷和铂为基础的chemotherapy.Patients和methodsMulti-country multisite前瞻性纵向观察研究。患者在化疗开始前和化疗期间每3周进行一次评估,最多持续6个周期,并在6、9和12个月时使用基于临床医师的量表进行评估(NCI-CTCAE; WHO-CIPN标准),客观评估(棉絮试验; 10 g单丝);患者报告的结局指标(FACT/GOG-Ntx; EORTC-CIPN 20)和神经传导研究.ResultsIn总数,343例患者被招募在队列中,提供2399观察。使用不同的评估方法,CIPN患病率差异很大(14.2-53.4%)。感觉神经病变(和相关症状特征)的患病率在每种类型的化疗中也不同,紫杉醇(高达63%)和奥沙利铂(高达71.4%)在大多数评估中显示出最高的CIPN发生率和更复杂的症状特征。患病率高峰出现在6个月评估前后(高达71.4%)。运动神经毒性常见,尤其是在多西他赛亚组中(高达22.1%;通过NCI-CTCAE检测)。各量表之间的相关性为中-低相关(r(s)= 0.15,p
BackgroundThere are inconsistencies in the literature regarding the prevalence and assessment of chemotherapy-induced peripheral neuropathy (CIPN). This study explored CIPN natural history and its characteristics in patients receiving taxane- and platinum-based chemotherapy.Patients and methodsMulti-country multisite prospective longitudinal observational study. Patients were assessed before commencing and three weekly during chemotherapy for up to six cycles, and at 6,9, and 12months using clinician-based scales (NCI-CTCAE; WHO-CIPN criterion), objective assessments (cotton wool test;10g monofilament); patient-reported outcome measures (FACT/GOG-Ntx; EORTC-CIPN20), and Nerve Conduction Studies.ResultsIn total, 343 patients were recruited in the cohort, providing 2399 observations. There was wide variation in CIPN prevalence rates using different assessments (14.2-53.4%). Prevalence of sensory neuropathy (and associated symptom profile) was also different in each type of chemotherapy, with paclitaxel (up to 63%) and oxaliplatin (up to 71.4%) showing the highest CIPN rates in most assessments and a more complex symptom profile. Peak prevalence was around the 6-month assessment (up to 71.4%). Motor neurotoxicity was common, particularly in the docetaxel subgroup (up to 22.1%; detected by NCI-CTCAE). There were relatively moderately-to-low correlations between scales (r(s)=0.15,p