Zahrieh David, Satele Daniel, Smith Ellen M Lavoie, Loprinzi Charles L, Le-Rademacher Jennifer
Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN 55905, USA.
Department of Acute, Chronic, and Continuing Care, University of Alabama at Birmingham School of Nursing, Birmingham, AL 35294, USA.
Cancers (Basel). 2022 Feb 25;14(5):1212. doi: 10.3390/cancers14051212.
While oxaliplatin-induced peripheral neuropathy (OIPN) is more common and severe in patients who receive the previous standard, 6-month oxaliplatin-based treatment, we hypothesized that OIPN was still pervasive in patients who received shorter, 3-month-treatment regimens. Using six EORTC QLQ-CIPN20 questions that quantify numbness (N), tingling (T) and shooting/burning pain (P) in upper/lower distal extremities, our aim is to quantify patient-reported responses over 3 months (6 cycles) of oxaliplatin regarding symptom-specific timing, location and severity. For each question, patients were asked how each of the sensory symptoms had affected them during the preceding week, with 1 = “Not at all”, 2 = “A little”, 3 = “Quite a bit” and 4 = “Very much”. The proportional odds model for the cumulative log odds of response that allowed symptom-specific patient heterogeneity to be obtained was applied to a pooled dataset from the placebo arms of two multisite OIPN prevention trials and fit separately to the upper/lower distal extremities. For each symptom, we report the cycle-specific marginal probabilities for each response. In 141 patients, substantial patient heterogeneity in the likelihood, at a given cycle, of a more severe response for a symptom was present. Distinct patterns in the probabilities for each response over time for N and T were observed between the upper/lower distal extremities, while the probabilities of a response >1 for P was largely negligible in both locations. Despite the decrease in exposure to oxaliplatin from 6 to 3 months, OIPN was still pervasive with patients experiencing considerable N and T in the fingers (or hands) and toes (or feet).
虽然在接受以往标准的基于奥沙利铂的6个月治疗方案的患者中,奥沙利铂诱导的周围神经病变(OIPN)更为常见且严重,但我们推测在接受较短的3个月治疗方案的患者中,OIPN仍然普遍存在。我们使用欧洲癌症研究与治疗组织(EORTC)的六个QLQ-CIPN20问题来量化上下肢远端的麻木(N)、刺痛(T)和射痛/灼痛(P),目的是量化患者报告的在3个月(6个周期)奥沙利铂治疗期间症状的特定时间、位置和严重程度的反应。对于每个问题,询问患者在前一周每种感觉症状对他们的影响程度,1 = “完全没有”,2 = “有一点”,3 = “相当多”,4 = “非常严重”。将允许获得症状特异性患者异质性的反应累积对数几率的比例优势模型应用于来自两项多中心OIPN预防试验安慰剂组的汇总数据集,并分别拟合到上下肢远端。对于每种症状,我们报告每个反应的特定周期边际概率。在141名患者中,在给定周期内症状出现更严重反应的可能性存在显著的患者异质性。在上下肢远端之间观察到N和T随时间的每个反应概率的不同模式,而在两个部位P反应>1的概率在很大程度上可以忽略不计。尽管奥沙利铂的暴露时间从6个月减少到3个月,但OIPN仍然普遍存在,患者在手指(或手)和脚趾(或脚)出现相当程度的N和T。