Sueyoshi Shintaro, Ono Takeharu, Chitose Shun-Ichi, Fukahori Mioko, Kurita Takashi, Umeno Hirohito
Department of Otolaryngology-Head and Neck Surgery, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
J Oncol Pharm Pract. 2025 Mar;31(2):195-202. doi: 10.1177/10781552231225933. Epub 2024 Jan 22.
ObjectiveCetuximab is a molecular targeted drug that targets epithelial growth factor receptors. The skin toxicity of cetuximab arising from epithelial growth factor inhibition is well known. Some patients with cetuximab therapy decided to make central venous port during the long-term intravenous treatments. Therefore, the author hypothesized that cetuximab administration might increase the risk of central venous port-related infection due to damage to skin barrier function. The main aim of the present study was to investigate the relationship between cetuximab administration and central venous port-related infection.MethodsA total of 83 patients had a central venous port placed from 2016 through 2021. We analyzed, retrospectively, the relationship between cetuximab therapy and the incidence of central venous port-related infection involving central line-associated bloodstream infection and pocket infection. Additionally, the risk factors of central venous port-related infection were examined in the population undergoing cetuximab therapy.ResultsIn total populations (83 cases), central line-associated bloodstream infection happened in five patients (6%) and pocket infection happened in six patients (7%) after central venous port placement. In the cetuximab therapy group (45 cases), there were four patients with central line-associated bloodstream infection (9%) and six with pocket infection (13%). The pocket infection happened more frequently in the cetuximab group than the other group with significant differences. Additionally, in the cetuximab group, the patients who had an interval of less than seven days between central venous port placement and cetuximab dosing, or central venous port placement preceded by cetuximab dosing had more pocket infection with significant differences.ConclusionSkin complications after the central venous port placement were related to cetuximab administration and the timing of cetuximab therapy.
目的
西妥昔单抗是一种靶向表皮生长因子受体的分子靶向药物。西妥昔单抗因抑制表皮生长因子而产生的皮肤毒性是众所周知的。一些接受西妥昔单抗治疗的患者在长期静脉治疗期间决定置入中心静脉导管。因此,作者推测西妥昔单抗给药可能会因皮肤屏障功能受损而增加中心静脉导管相关感染的风险。本研究的主要目的是调查西妥昔单抗给药与中心静脉导管相关感染之间的关系。
方法
2016年至2021年期间,共有83例患者置入了中心静脉导管。我们回顾性分析了西妥昔单抗治疗与中心静脉导管相关感染(包括中心静脉导管相关血流感染和囊袋感染)发生率之间的关系。此外,还对接受西妥昔单抗治疗的人群中中心静脉导管相关感染的危险因素进行了检查。
结果
在全部83例患者中,中心静脉导管置入后,5例患者(6%)发生了中心静脉导管相关血流感染,6例患者(7%)发生了囊袋感染。在西妥昔单抗治疗组(45例)中,有4例患者发生中心静脉导管相关血流感染(9%),6例患者发生囊袋感染(13%)。西妥昔单抗组囊袋感染的发生率高于其他组,差异有统计学意义。此外,在西妥昔单抗组中,中心静脉导管置入与西妥昔单抗给药间隔小于7天或在西妥昔单抗给药后进行中心静脉导管置入的患者囊袋感染更多,差异有统计学意义。
结论
中心静脉导管置入后的皮肤并发症与西妥昔单抗给药及西妥昔单抗治疗的时机有关。