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首页> 外文期刊>Chinese journal of cancer >Prognostic significance of the pre-chemotherapy lymphocyte-to-monocyte ratio in patients with previously untreated metastatic colorectal cancer receiving FOLFOX chemotherapy
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Prognostic significance of the pre-chemotherapy lymphocyte-to-monocyte ratio in patients with previously untreated metastatic colorectal cancer receiving FOLFOX chemotherapy

机译:接受FOLFOX化疗的未接受治疗的转移性结直肠癌患者化疗前淋巴细胞与单核细胞比率的预后意义

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BackgroundAs a surrogate marker of systemic inflammation, the lymphocyte-to-monocyte ratio (LMR) is an independent prognostic factor for various malignancies. This study investigated the prognostic significance of the pre-chemotherapy LMR in patients with previously untreated metastatic colorectal cancer (mCRC) receiving chemotherapy. MethodsThe present study included newly diagnosed mCRC patients treated between January 2005 and December 2013 with FOLFOX chemotherapy, specifically oxaliplatin 180?mg/m2 on day 1, with leucovorin 400?mg/m2 administered as a 2-hour infusion before the administration of 5-fluorouracil 400?mg/m2 as an intravenous bolus injection, and 5-fluorouracil 2400?mg/m2 as a 46-h infusion immediately after 5-fluorouracil bolus injection. The LMR was calculated as the absolute count of lymphocytes divided by the absolute count of monocytes. COX proportional hazards analysis was performed to evaluate the association of LMR with survival outcomes. ResultsA total of 488 patients were included. Patients with high pre-chemotherapy LMR experienced significant improvements in progression-free survival (PFS, 9.2 vs. 7.6?months, P ConclusionsFor patients with previously untreated mCRC receiving FOLFOX chemotherapy, an elevated pre-chemotherapy LMR is an independent favorable prognostic factor for PFS and OS, and changes in the LMR before and after chemotherapy seem to predict the benefit of chemotherapy.
机译:背景技术作为全身性炎症的替代指标,淋巴细胞与单核细胞的比率(LMR)是各种恶性肿瘤的独立预后因素。这项研究调查了化疗前LMR对以前未经治疗的转移性结直肠癌(mCRC)接受化疗的患者的预后意义。方法:本研究包括2005年1月至2013年12月之间接受FOLFOX化疗的新诊断的mCRC患者,特别是第1天的奥沙利铂180?mg / m 2 和亚叶酸400?mg / m 2 < / sup> 2小时输注,然后静脉推注5-氟尿嘧啶400?mg / m 2 和5-氟尿嘧啶2400?mg / m 2 < 5氟尿嘧啶推注后立即进行46小时输注。 LMR计算为淋巴细胞的绝对计数除以单核细胞的绝对计数。进行了COX比例风险分析,以评估LMR与生存结局的关系。结果共纳入488例患者。接受高化疗前LMR的患者的无进展生存期显着改善(PFS,9.2 vs. 7.6?months,P结论)对于先前未接受过FOLFOX化疗的mCRC患者而言,高化疗前LMR是PFS的独立有利预后因素和OS,以及化疗前后LMR的变化似乎预示了化疗的益处。

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