Department of Pediatric Hematology and Oncology, Dr. Behçet Uz Children's Hospital, Izmir, Turkey.
Department of Pediatric Neurology, Dr. Behçet Uz Children's Hospital, Izmir, Turkey.
Neurol Sci. 2021 Sep;42(9):3681-3686. doi: 10.1007/s10072-020-04970-w. Epub 2021 Jan 13.
Vincristine (VCR), which is a key component of chemotherapy, is important for survival. VCR is associated with a well-known side effect, including neurotoxicity.
The aim of this study was to evaluate the features of vincristine-induced peripheral neuropathy (VIPN) and the effectiveness of pyridoxine plus pyridostigmine therapy in children with acute lymphoblastic leukemia.
The WHO and NCI CTCAE neurotoxicity scorings were used to evaluate VIPN at diagnosis, in the first month, and after the third month of the treatment. The clinical features of 23 patients having acute lymphoblastic leukemia with VIPN during the period of July 2013-February 2016 were prospectively evaluated.
The mean age was 72.8 ± 51.6 months, and 26.1%, 56.5%, and 17.4% were in standard, moderate, and high-risk groups, respectively. Neuropathy frequently occurred at induction (82.6%) and reinduction (17.4%) of the protocol. Drop foot (82.6%), leg pain (82.6%), and difficulty in walking (82.6%) were observed. The mean total cumulative dose of neuropathy occurrence was 5.6 ± 2.03 mg/m. Our study showed that both the WHO and NCI CTCAE scorings were significantly improved via pyridoxine plus pyridostigmine therapy.
The WHO and NCI CTCAE scorings may be used for evaluating neuropathy at diagnosis and follow-up of neurotoxicity with treatment. Pyridoxine plus pyridostigmine therapy may be an effective option in the treatment of VIPN.
长春新碱(VCR)是化疗的关键组成部分,对生存至关重要。VCR 与一种众所周知的副作用有关,包括神经毒性。
本研究旨在评估长春新碱诱导的周围神经病变(VIPN)的特征,以及吡哆醇加吡啶斯的明治疗在儿童急性淋巴细胞白血病中的疗效。
采用 WHO 和 NCI CTCAE 神经毒性评分标准,分别于诊断时、治疗第 1 个月和第 3 个月评估 VIPN。前瞻性评估 2013 年 7 月至 2016 年 2 月期间患有 VIPN 的 23 例急性淋巴细胞白血病患者的临床特征。
平均年龄为 72.8 ± 51.6 个月,分别有 26.1%、56.5%和 17.4%处于标准、中危和高危组。神经病变在方案诱导(82.6%)和再诱导(17.4%)时经常发生。足下垂(82.6%)、腿部疼痛(82.6%)和行走困难(82.6%)是常见的表现。发生神经病变的总累积剂量为 5.6 ± 2.03mg/m。本研究表明,吡哆醇加吡啶斯的明治疗可显著改善 WHO 和 NCI CTCAE 评分。
WHO 和 NCI CTCAE 评分可用于评估神经毒性治疗时的诊断和随访中的神经病变。吡哆醇加吡啶斯的明治疗可能是治疗 VIPN 的有效选择。