Abrahão Renata, Cooley Julianne J P, Kahn Justine M, Brunson Ann, Alvarez Elysia M, Mahajan Anjlee, Wun Ted, Verma Rashmi, Ruddy Kathryn J, Keegan Theresa H M
Division of Hematology and Oncology, Center for Oncology Hematology Outcomes Research and Training (COHORT), University of California Davis Comprehensive Cancer Center, Sacramento, CA.
California Cancer Reporting and Epidemiologic Surveillance Program, University of California Davis Comprehensive Cancer Center, Sacramento, CA.
JCO Oncol Pract. 2025 Apr 22:OP2400748. doi: 10.1200/OP-24-00748.
Chemotherapy-induced peripheral neuropathy is a potentially debilitating adverse effect of cancer therapy that can lead to delay, reduction, or discontinuation of cancer treatment. Population-based data on peripheral neuropathy incidence among young cancer survivors are lacking.
Using a linkage between Medicaid, the California Cancer Registry, and hospitalization and emergency department data, we identified 6,028 adolescents and young adults (15-39 years) with Hodgkin lymphoma (HL), non-Hodgkin lymphoma (NHL), breast cancer, colorectal cancer, or testicular cancer and 418 children (<15 years) with HL or NHL during 2005-2017. We determined the cumulative incidence of peripheral neuropathy and its association with neurotoxic chemotherapy identified from Medicaid claims, using multivariable Cox proportional hazards regression models.
Of 6,446 patients, 1,007 were diagnosed with peripheral neuropathy. Across each cancer type, incidence was higher among patients receiving neurotoxic drugs. For example, compared with non-neurotoxic agents, 5-year cumulative incidence was higher with oxaliplatin for colorectal cancer (24.0% 6.2%) and paclitaxel for breast cancer (22.6% 5.1%). In multivariable analysis, the agents most strongly associated with peripheral neuropathy were brentuximab (±other neurotoxic drugs) for HL (hazard ratio [HR], 9.53 [95% CI, 5.95 to 15.26]); brentuximab (±vinca alkaloids; HR, 7.00 [95% CI, 4.13 to 11.87]) for NHL, paclitaxel for breast cancer (HR, 4.03 [95% CI, 3.05 to 5.31]); oxaliplatin for colorectal cancer (HR, 3.46 [95% CI, 2.23 to 5.36]); and cisplatin and etoposide for testicular cancer (HR, 2.06 [95% CI, 1.37 to 3.11]).
The high incidence of peripheral neuropathy highlights the need for frequent monitoring, new supportive care approaches, and development of novel therapeutic agents to minimize toxicity while maintaining treatment efficacy.
化疗引起的周围神经病变是癌症治疗中一种潜在的使人衰弱的不良反应,可导致癌症治疗的延迟、减少或中断。目前缺乏关于年轻癌症幸存者周围神经病变发病率的基于人群的数据。
利用医疗补助计划、加利福尼亚癌症登记处以及住院和急诊科数据之间的关联,我们确定了2005年至2017年期间6028名患有霍奇金淋巴瘤(HL)、非霍奇金淋巴瘤(NHL)、乳腺癌、结直肠癌或睾丸癌的青少年和青年(15 - 39岁)以及418名患有HL或NHL的儿童(<15岁)。我们使用多变量Cox比例风险回归模型确定周围神经病变的累积发病率及其与从医疗补助计划索赔中识别出的神经毒性化疗的关联。
在6446名患者中,1007名被诊断患有周围神经病变。在每种癌症类型中,接受神经毒性药物治疗的患者发病率更高。例如,与非神经毒性药物相比,结直肠癌使用奥沙利铂的5年累积发病率更高(24.0% 6.2%),乳腺癌使用紫杉醇的5年累积发病率更高(22.6% 5.1%)。在多变量分析中,与周围神经病变关联最密切的药物是用于HL的brentuximab(±其他神经毒性药物)(风险比[HR],9.53 [95%置信区间,5.95至15.26]);用于NHL的brentuximab(±长春花生物碱;HR,7.00 [95%置信区间,4.13至11.87]),用于乳腺癌的紫杉醇(HR,4.03 [95%置信区间,3.05至5.31]);用于结直肠癌的奥沙利铂(HR,3.46 [95%置信区间,2.23至5.36]);以及用于睾丸癌的顺铂和依托泊苷(HR,2.06 [95%置信区间,1.37至3.11])。
周围神经病变的高发病率凸显了频繁监测、新的支持性护理方法以及开发新型治疗药物的必要性,以在维持治疗效果的同时将毒性降至最低。