Keum Jiyoung, Lee Hee Seung, Jo Jung Hyun, Chung Moon Jae, Park Jeong Youp, Park Seung Woo, Song Si Young, Bang Seungmin
Division of Gastroenterology, Department of Internal Medicine, Institute of Gastroenterology, Yonsei University College of Medicine, Seoul 03722, Korea.
Division of Gastroenterology, Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul 07985, Korea.
Cancers (Basel). 2022 Feb 28;14(5):1244. doi: 10.3390/cancers14051244.
FOLFIRINOX (oxaliplatin, leucovorin, irinotecan, and 5-fluorouracil) is a first-line chemotherapy for metastatic pancreatic cancer (PC). Chemotherapy-induced neutropenia is one of the most serious adverse events associated with advanced PC. Although polymorphisms are associated with the metabolism of irinotecan, their role as surrogate markers for FOLFIRINOX-induced neutropenia has not been confirmed. We investigated risk factors for FN-in particular, polymorphisms-in PC patients receiving FOLFIRINOX, using a single-center cohort registry. To investigate the association between polymorphisms and FN, we divided patients into three groups based on the predicted phenotype: extensive metabolizer (EM) vs. intermediate metabolizer (IM) vs. poor metabolizer (PM). A total of 154 patients (FN group ( = 31) vs. non-FN group ( = 123)) receiving first-line FOLFIRINOX were identified between December 2017 and July 2020. The Cox regression analysis showed that female sex (HR: 2.20; = 0.031), Eastern Cooperative Oncology Group performance status = 1 (HR: 2.83; = 0.008), IM (HR: 4.30; = 0.004), and PM (HR: 4.03; = 0.028) were statistically significant risk factors for FN. We propose that is the strongest predictive factor for FN and that this gene should be screened prior to the administration of chemotherapy.
FOLFIRINOX(奥沙利铂、亚叶酸钙、伊立替康和5-氟尿嘧啶)是转移性胰腺癌(PC)的一线化疗方案。化疗引起的中性粒细胞减少是晚期PC最严重的不良事件之一。尽管基因多态性与伊立替康的代谢有关,但其作为FOLFIRINOX诱导的中性粒细胞减少替代标志物的作用尚未得到证实。我们使用单中心队列登记研究了接受FOLFIRINOX治疗的PC患者发生中性粒细胞减少(FN)的危险因素,尤其是基因多态性。为了研究基因多态性与FN之间的关联,我们根据预测的表型将患者分为三组:广泛代谢型(EM)与中间代谢型(IM)与慢代谢型(PM)。在2017年12月至2020年7月期间,共确定了154例接受一线FOLFIRINOX治疗的患者(FN组(n = 31)与非FN组(n = 123))。Cox回归分析显示,女性(HR:2.20;P = 0.031)、东部肿瘤协作组体能状态= 1(HR:2.83;P = 0.008)、IM(HR:4.30;P = 0.004)和PM(HR:4.03;P = 0.028)是FN的统计学显著危险因素。我们提出,某基因是FN最强的预测因素,在化疗给药前应筛查该基因。 (注:原文中“polymorphisms”和“ is”处表述不太准确,推测原文可能是想表达“某些基因多态性”和“某个基因多态性”之类的意思,但按给定原文翻译如上。)