首页> 美国卫生研究院文献>Molecular and Clinical Oncology >Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan with or without molecularly-targeted drugs
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Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan with or without molecularly-targeted drugs

机译:血清铁水平是使用亚叶酸和氟尿嘧啶加奥沙利铂或亚叶酸钙或亚叶酸和氟尿嘧啶加伊立替康联合化疗的新生物标志物有或没有分子靶向药物

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摘要

Serum iron levels have been reported to increase following the administration of various anticancer drugs. An increase in serum iron levels during therapy with leucovorin and fluorouracil plus oxaliplatin (FOLFOX) or leucovorin and fluorouracil plus irinotecan (FOLFIRI) was also observed. The aim of this study was to investigate the correlation between serum iron levels and prognosis in advanced colorectal cancer (CRC) patients treated with FOLFOX/FOLFIRI ± molecularly-targeted drugs. Serum iron levels were measured prior to and at 48 h after treatment with FOLFOX/FOLFIRI ± molecularly-targeted drugs in 72 advanced CRC patients, all of whom succumbed to the disease between December, 2005 and February, 2012. No patients received radiotherapy. Taking the median rate of increase in serum iron levels as the cut-off value in each therapy, the patients were divided into cohort I (increase rate greater than the cut-off value in at least one therapy) or cohort II (increase rate less than the cut-off value in all therapies). The χ2 test and the t-test were used to compare patient characteristics between the two cohorts. Prognosis was evaluated between the two cohorts using the Kaplan-Meier method, the log-rank test and the Cox proportional hazards regression analysis. No significant bias in patient characteristics (including the frequency of chemotherapy or number of patients treated with molecularly-targeted drugs) was observed between the two cohorts. Serum iron levels were transiently elevated following treatment (P<0.001), returning to baseline within 2 weeks. Median survival time (MST) in cohort I (n=44) and cohort II (n=28) was 430 and 377 days, respectively. The MST was significantly higher in cohort I (P=0.0382). The multivariate analysis identified a small increase in serum iron levels as an independent risk factor for overall survival (OS). These results suggest that serum iron levels may be used as a new predictive factor in FOLFOX/FOLFIRI ± molecularly-targeted drug therapy. Serum iron levels may therefore prove to be a useful and convenient biomarker for OS in CRC patients.
机译:据报道,服用各种抗癌药物后血清铁水平会升高。在用亚叶酸和氟尿嘧啶加奥沙利铂(FOLFOX)或亚叶酸和氟尿嘧啶加伊立替康(FOLFIRI)治疗期间,血清铁水平也有所升高。这项研究的目的是研究用FOLFOX / FOLFIRI±分子靶向药物治疗的晚期大肠癌(CRC)患者血清铁水平与预后之间的相关性。在72名晚期CRC患者中,使用FOLFOX / FOLFIRI±分子靶向药物治疗之前和之后48小时测量了血清铁水平,所有这些患者均于2005年12月至2012年2月死于该病。没有患者接受放疗。将血清铁水平升高的中位数速率作为每种疗法的临界值,将患者分为第一组(至少一种疗法中的升高率大于临界值)或第二组(较低的增长率)高于所有疗法的临界值)。 χ 2 检验和t检验用于比较两个队列的患者特征。使用Kaplan-Meier方法,对数秩检验和Cox比例风险回归分析评估了两个队列之间的预后。在这两个队列之间,未观察到患者特征(包括化学疗法的频率或接受分子靶向药物治疗的患者数量)有明显偏倚。治疗后血清铁水平暂时升高(P <0.001),并在2周内恢复至基线。第一组(n = 44)和第二组(n = 28)的中位生存时间(MST)分别为430天和377天。在队列I中,MST显着更高(P = 0.0382)。多元分析确定血清铁水平的少量升高是整体生存(OS)的独立危险因素。这些结果表明,血清铁水平可作为FOLFOX / FOLFIRI±分子靶向药物治疗中的新预测因子。因此,血清铁水平可能被证明是CRC患者OS的有用且方便的生物标志物。

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