Hershman Dawn L, Till Cathee, Wright Jason D, Awad Danielle, Ramsey Scott D, Barlow William E, Minasian Lori M, Unger Joseph
Dawn L. Hershman, Jason D. Wright, and Danielle Awad, Columbia University Medical Center, New York, NY; Cathee Till, Scott D. Ramsey, and Joseph Unger, Fred Hutchinson Cancer Research Center; William E. Barlow, University of Washington, Seattle, WA; and Lori M. Minasian, National Cancer Institute, Bethesda, MD.
J Clin Oncol. 2016 Sep 1;34(25):3014-22. doi: 10.1200/JCO.2015.66.2346. Epub 2016 Jun 20.
Neuropathy is a debilitating toxicity associated with various chemotherapy agents. We evaluated the association between common comorbid conditions and the development of peripheral neuropathy in patients treated with taxane-based chemotherapy.
We examined the Southwest Oncology Group database to identify phase II and III trials that included taxane therapy from 1999 to 2011. We linked the Southwest Oncology Group clinical records to Medicare claims data according to Social Security number, sex, and date of birth. The following disease conditions potentially associated with peripheral neuropathy were evaluated: diabetes, hypothyroidism, hypercholesterolemia, hypertension, varicella zoster, peripheral vascular disease, and autoimmune diseases. Multivariate logistic regression was used to model the odds of experiencing grade 2 to 4 neuropathy.
A total of 1,401 patients from 23 studies were included in the analysis. Patients receiving paclitaxel were more likely to experience grade 2 to 4 neuropathy compared with docetaxel (25% v 12%, respectively; OR, 2.20; 95% CI, 1.52 to 3.18; P < .001). The inclusion of a platinum agent was also associated with greater neuropathy (OR, 1.68; 95% CI, 1.18 to 2.40; P = .004). For each increase in age of 1 year, the odds of neuropathy increased 4% (P = .006). Patients with complications from diabetes had more than twice the odds of having neuropathy (OR, 2.13; 95% CI, 1.31 to 3.46; P = .002) compared with patients with no diabetes. In contrast, patients with autoimmune disease were half as likely to experience neuropathy (OR, 0.49; 95% CI, 0.24 to 1.02; P = .06). The other conditions were not associated with neuropathy.
We found that in addition to drug-related factors, age and history of diabetes were independent predictors of the development of chemotherapy-induced peripheral neuropathy. Interestingly, we also observed that a history of autoimmune disease was associated with reduced odds of neuropathy. Patients with diabetic complications may choose to avoid paclitaxel or taxane plus platinum combination therapies if other efficacious options exist.
神经病变是一种与多种化疗药物相关的使人衰弱的毒性反应。我们评估了常见合并症与接受紫杉烷类化疗患者发生周围神经病变之间的关联。
我们查阅了西南肿瘤协作组数据库,以确定1999年至2011年期间包含紫杉烷治疗的II期和III期试验。我们根据社会保险号、性别和出生日期将西南肿瘤协作组的临床记录与医疗保险理赔数据相链接。对以下可能与周围神经病变相关的疾病状况进行了评估:糖尿病、甲状腺功能减退、高胆固醇血症、高血压、水痘带状疱疹、周围血管疾病和自身免疫性疾病。采用多因素逻辑回归模型来模拟发生2至4级神经病变的几率。
分析纳入了来自23项研究的1401例患者。与多西他赛相比,接受紫杉醇治疗的患者更有可能发生2至4级神经病变(分别为25%和12%;比值比[OR]为2.20;95%置信区间[CI]为1.52至3.18;P <.001)。联合使用铂类药物也与更高的神经病变发生率相关(OR为1.68;95% CI为1.18至2.40;P = 0.004)。年龄每增加1岁,发生神经病变的几率增加4%(P = 0.006)。与无糖尿病患者相比,有糖尿病并发症的患者发生神经病变的几率高出两倍多(OR为2.13;95% CI为1.31至3.46;P = 0.002)。相比之下,有自身免疫性疾病的患者发生神经病变的可能性只有一半(OR为0.49;95% CI为0.24至1.02;P = 0.06)。其他疾病状况与神经病变无关。
我们发现,除了药物相关因素外,年龄和糖尿病史是化疗引起的周围神经病变发生的独立预测因素。有趣的是,我们还观察到自身免疫性疾病史与神经病变几率降低有关。如果存在其他有效选择,有糖尿病并发症的患者可能会选择避免使用紫杉醇或紫杉烷加铂类联合疗法。