Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Germany.
Department of Pediatric Neurology, Psychosomatics and Pain Therapy, Klinikum Stuttgart-Olgahospital, Germany; German Pain Center, Children's Pain Therapy & Paediatric Palliative Care, University of Witten, Herdecke, Germany.
Eur J Paediatr Neurol. 2018 May;22(3):457-469. doi: 10.1016/j.ejpn.2017.12.019. Epub 2018 Jan 5.
Chemotherapy-induced Peripheral Neuropathy (CIPN) of large-fibers affects up to 20% of survivors of pediatric acute lymphoblastic leukemia (ALL). We aimed to describe small-fiber toxicity and pain sensitization in this group.
In a cross-sectional, bicentric study we assessed 46 survivors of pediatric ALL (Mean age: 5.7 ± 3.5 years at diagnosis, median 2.5 years after therapy; males: 28).
≥6 years of age, ≥3 months after last administration of Vincristine, and cumulative dose of Vincristine 12 mg/m. We used a reduced version of the Pediatric-modified Total Neuropathy Score (Ped-mTNS) as bedside test and Quantitative Sensory Testing (QST) for assessment of small- and large-fiber neuropathy as well as pain sensitization. We employed Nerve Conduction Studies (NCS) as the most accurate tool for detecting large-fiber neuropathy.
Fifteen survivors (33%) had abnormal rPed-mTNS values (≥4 points) and 5 survivors (11%) reported pain. In QST, the survivor group showed significant (p < 0.001) inferior large-fiber function and pain sensitization when compared to healthy matched peers. We identified deficits of vibration in 33 (72%) and tactile hypoesthesia in 29 (63%), hyperalgesia to blunt pressure in 19 (41%), increased mechanical pain sensitivity in 12 (26%) and allodynia in 16 (35%) of 46 survivors. Only 7 survivors (15%) had pathologic NCS.
QST is a sensitive tool that revealed signs of large-fiber neuropathy in two thirds, small-fiber neuropathy and pain sensitization in one third of survivors. Prospective studies using QST in pediatric oncology may help to elucidate the pathophysiology of small-fiber neuropathy and pain sensitization as well as their relevance for quality of survival.
大纤维化疗诱导的周围神经病(CIPN)影响多达 20%的儿童急性淋巴细胞白血病(ALL)幸存者。我们旨在描述这一组的小纤维毒性和疼痛敏化。
在一项横断面、双中心研究中,我们评估了 46 名儿童 ALL 幸存者(诊断时平均年龄为 5.7±3.5 岁,治疗后中位数为 2.5 年;男性 28 名)。
年龄≥6 岁,末次长春新碱给药后≥3 个月,累积长春新碱剂量≥12mg/m。我们使用简化的儿科改良总神经病变评分(Ped-mTNS)作为床边测试,以及定量感觉测试(QST)来评估小纤维和大纤维神经病以及疼痛敏化。我们使用神经传导研究(NCS)作为检测大纤维神经病最准确的工具。
15 名幸存者(33%)的 rPed-mTNS 值异常(≥4 分),5 名幸存者(11%)报告疼痛。在 QST 中,与健康匹配的同龄人相比,幸存者组表现出明显(p<0.001)的大纤维功能和疼痛敏化降低。我们发现 33 名幸存者(72%)存在振动感觉缺失,29 名幸存者(63%)存在触觉感觉减退,19 名幸存者(41%)存在钝压性痛觉过敏,12 名幸存者(26%)存在机械性疼痛敏感性增加,16 名幸存者(35%)存在感觉异常。只有 7 名幸存者(15%)的 NCS 异常。
QST 是一种敏感的工具,它在三分之二的幸存者中发现了大纤维神经病的迹象,在三分之一的幸存者中发现了小纤维神经病和疼痛敏化的迹象。在儿科肿瘤学中使用 QST 的前瞻性研究可能有助于阐明小纤维神经病和疼痛敏化的病理生理学及其对生存质量的相关性。