Maksten Eva Futtrup, Mørch Carsten Dahl, Jakobsen Lasse Hjort, Kragholm Kristian Hay, Blindum Pernille From, Simonsen Mikkel Runason, Ejskjaer Niels, Dybkær Karen, Gregersen Henrik, Madsen Jakob, El-Galaly Tarec C, Severinsen Marianne Tang
Research Section, Department of Hematology, Clinical Cancer Research Center, Aalborg University Hospital, Sdr. Skovvej 15, 9000, Aalborg, Denmark.
Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Support Care Cancer. 2025 Feb 26;33(3):225. doi: 10.1007/s00520-025-09282-3.
To assess and describe chemotherapy-induced peripheral neuropathy (CIPN), a well-known complication to cancer treatment, using different methodologies in hematological patients.
Patients scheduled for treatment with vincristine, bortezomib, or lenalidomide were included in this longitudinal observational study. The patients were examined for CIPN before treatment (baseline), before each chemotherapy cycle, one month after end of treatment, and one year after baseline using patient-reported outcomes (Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Ntx-13 (FACT/GOG-Ntx-13)) and clinician-assessed outcomes (the Common Terminology Criteria for Adverse Events (CTCAE) and the Total Neuropathy Score-clinical version (TNSc©)).
A total of 23 patients with 171 examination visits were included between 2020 and 2022. Four patients were treated with vincristine, five with bortezomib, and fourteen with bortezomib and lenalidomide combined. Defining CIPN as a ≥ 10% decrease in the FACT/GOG-Ntx-13, 11 patients (47.8%) developed CIPN during treatment and follow-up. CTCAE score for paresthesia increased from baseline throughout treatment until 1 month after the last treatment (p ≤ 0.045). Overall, the highest proportion of CIPN was present at cycle 3-4 and 1 month after last treatment.
This study describes the course of CIPN in patients treated with vincristine, bortezomib, or lenalidomide using both patient-reported and clinician-assessed outcomes. The highest proportion of CIPN was present at cycle 3-4 and 1 month after treatment, at which timepoints clinicians must be especially aware of CIPN.
Registered at Clinicaltrials.gov (Trial Registration Number: NCT04393363) on March 19, 2020.
采用不同方法评估和描述化疗引起的周围神经病变(CIPN),这是癌症治疗中一种众所周知的并发症,研究对象为血液系统疾病患者。
本纵向观察性研究纳入了计划接受长春新碱、硼替佐米或来那度胺治疗的患者。在治疗前(基线)、每个化疗周期前、治疗结束后1个月以及基线后1年,使用患者报告结局(癌症治疗功能评估/妇科肿瘤学组-Ntx-13(FACT/GOG-Ntx-13))和临床医生评估结局(不良事件通用术语标准(CTCAE)和总神经病变评分-临床版(TNSc©))对患者进行CIPN检查。
2020年至2022年期间共纳入23例患者,进行了171次检查。4例患者接受长春新碱治疗,5例接受硼替佐米治疗,14例接受硼替佐米和来那度胺联合治疗。将CIPN定义为FACT/GOG-Ntx-13降低≥10%,11例患者(47.8%)在治疗和随访期间发生CIPN。感觉异常的CTCAE评分从基线开始在整个治疗过程中升高,直至最后一次治疗后1个月(p≤0.045)。总体而言,CIPN比例最高出现在第3 - 4周期和最后一次治疗后1个月。
本研究使用患者报告和临床医生评估的结局描述了接受长春新碱、硼替佐米或来那度胺治疗的患者CIPN的病程。CIPN比例最高出现在第3 - 4周期和治疗后1个月,此时临床医生必须特别注意CIPN。
于2020年3月19日在Clinicaltrials.gov注册(试验注册号:NCT04393363)。