{"title":"接受曲妥珠单抗治疗的乳腺癌患者发生输液反应的相关因素","authors":"Ryuji Yamaguchi, Masanobu Uchiyama, Motoyasu Miyazaki, Toshinobu Hayashi, Kohei Oyabu, Takafumi Nakano, Koichi Matsuo","doi":"10.21873/cdp.10387","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/aim: </strong>Trastuzumab (TRA) is a key drug in human epidermal growth factor receptor type 2 (HER2)-positive breast cancer treatment. Infusion reactions (IR) with TRA are frequently observed in practice. Although the efficacy of premedication has been previously reported, it remains uncommon. The probability of severe IR due to TRA is low; however, when it does occur, it is associated with patient discomfort and expenditure of medical resources. This study aimed to analyze the factors associated with the occurrence of IR in patients with breast cancer who received TRA.</p><p><strong>Patients and methods: </strong>We retrospectively studied 204 patients who underwent TRA for breast cancer treatment between September 2008 and June 2023, identifying factors influencing the occurrence of IR at the time of TRA administration.</p><p><strong>Results: </strong>A total of 182 patients were included in this study, and the incidence of IR was 25.8% (47/182 patients). Multiple logistic regression analysis showed that pertuzumab (PER) use, high alkaline phosphatase (ALP), and low high-density lipoprotein (HDL) cholesterol levels were associated with IR.</p><p><strong>Conclusion: </strong>IR should be considered when PER is combined with TRA. ALP and HDL cholesterol levels may be predictive markers of TRA-induced IR in patients with breast cancer.</p>","PeriodicalId":72510,"journal":{"name":"Cancer diagnosis & prognosis","volume":"4 6","pages":"722-728"},"PeriodicalIF":0.0000,"publicationDate":"2024-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11534052/pdf/","citationCount":"0","resultStr":"{\"title\":\"Factors Associated With Infusion Reactions in Patients With Breast Cancer Receiving Trastuzumab.\",\"authors\":\"Ryuji Yamaguchi, Masanobu Uchiyama, Motoyasu Miyazaki, Toshinobu Hayashi, Kohei Oyabu, Takafumi Nakano, Koichi Matsuo\",\"doi\":\"10.21873/cdp.10387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background/aim: </strong>Trastuzumab (TRA) is a key drug in human epidermal growth factor receptor type 2 (HER2)-positive breast cancer treatment. Infusion reactions (IR) with TRA are frequently observed in practice. Although the efficacy of premedication has been previously reported, it remains uncommon. The probability of severe IR due to TRA is low; however, when it does occur, it is associated with patient discomfort and expenditure of medical resources. This study aimed to analyze the factors associated with the occurrence of IR in patients with breast cancer who received TRA.</p><p><strong>Patients and methods: </strong>We retrospectively studied 204 patients who underwent TRA for breast cancer treatment between September 2008 and June 2023, identifying factors influencing the occurrence of IR at the time of TRA administration.</p><p><strong>Results: </strong>A total of 182 patients were included in this study, and the incidence of IR was 25.8% (47/182 patients). Multiple logistic regression analysis showed that pertuzumab (PER) use, high alkaline phosphatase (ALP), and low high-density lipoprotein (HDL) cholesterol levels were associated with IR.</p><p><strong>Conclusion: </strong>IR should be considered when PER is combined with TRA. ALP and HDL cholesterol levels may be predictive markers of TRA-induced IR in patients with breast cancer.</p>\",\"PeriodicalId\":72510,\"journal\":{\"name\":\"Cancer diagnosis & prognosis\",\"volume\":\"4 6\",\"pages\":\"722-728\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-11-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11534052/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer diagnosis & prognosis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21873/cdp.10387\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer diagnosis & prognosis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21873/cdp.10387","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景/目的:曲妥珠单抗(TRA)是治疗人表皮生长因子受体 2 型(HER2)阳性乳腺癌的关键药物。在实践中经常观察到使用 TRA 时出现输注反应(IR)。虽然之前已有关于预处理疗效的报道,但仍不常见。TRA导致严重输液反应的概率很低;然而,一旦发生,就会给患者带来不适并耗费医疗资源。本研究旨在分析接受 TRA 的乳腺癌患者发生 IR 的相关因素:我们对 2008 年 9 月至 2023 年 6 月间接受 TRA 治疗的 204 例乳腺癌患者进行了回顾性研究,找出了影响患者在接受 TRA 治疗时发生 IR 的因素:本研究共纳入 182 例患者,IR 发生率为 25.8%(47/182 例)。多元逻辑回归分析显示,使用百妥珠单抗(PER)、高碱性磷酸酶(ALP)和低高密度脂蛋白(HDL)胆固醇水平与IR有关:结论:PER 与 TRA 联用时应考虑 IR。ALP和高密度脂蛋白胆固醇水平可能是乳腺癌患者TRA诱发IR的预测指标。
Factors Associated With Infusion Reactions in Patients With Breast Cancer Receiving Trastuzumab.
Background/aim: Trastuzumab (TRA) is a key drug in human epidermal growth factor receptor type 2 (HER2)-positive breast cancer treatment. Infusion reactions (IR) with TRA are frequently observed in practice. Although the efficacy of premedication has been previously reported, it remains uncommon. The probability of severe IR due to TRA is low; however, when it does occur, it is associated with patient discomfort and expenditure of medical resources. This study aimed to analyze the factors associated with the occurrence of IR in patients with breast cancer who received TRA.
Patients and methods: We retrospectively studied 204 patients who underwent TRA for breast cancer treatment between September 2008 and June 2023, identifying factors influencing the occurrence of IR at the time of TRA administration.
Results: A total of 182 patients were included in this study, and the incidence of IR was 25.8% (47/182 patients). Multiple logistic regression analysis showed that pertuzumab (PER) use, high alkaline phosphatase (ALP), and low high-density lipoprotein (HDL) cholesterol levels were associated with IR.
Conclusion: IR should be considered when PER is combined with TRA. ALP and HDL cholesterol levels may be predictive markers of TRA-induced IR in patients with breast cancer.