首页> 外文期刊>Leukemia and lymphoma >Peripheral blood absolute lymphocyte/monocyte ratio during rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone treatment cycles predicts clinical outcomes in diffuse large B-cell lymphoma
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Peripheral blood absolute lymphocyte/monocyte ratio during rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone treatment cycles predicts clinical outcomes in diffuse large B-cell lymphoma

机译:利妥昔单抗,环磷酰胺,阿霉素,长春新碱和泼尼松治疗周期中的外周血绝对淋巴细胞/单核细胞比率预​​测弥漫性大B细胞淋巴瘤的临床结局

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摘要

A limitation of the prognostic factor peripheral blood absolute lymphocyte/monocyte ratio (ALC/AMC) at diagnosis in diffuse large B-cell lymphoma (DLBCL) is its inability to sequentially assess the host/tumor microenvironment interaction and clinical outcomes during treatment. Therefore, we studied the ALC/AMC ratio at each rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) cycle as a predictor for survival. We studied 107 consecutive patients with DLBCL diagnosed, treated only with R-CHOP and followed at the Mayo Clinic. Unsupervised hierarchical clustering identified four clusters based on the patterns of ALC/AMC ratio recovery during cycles. The most inferior survival was seen in the cluster with ALC/AMC ratio < 1.1 in all cycles. By multivariate analysis, ALC/AMC ratio < 1.1 during all cycles was an independent predictor for inferior overall survival and progression-free survival. The ALC/AMC ratio during R-CHOP cycles predicts survival and provides a platform to develop therapeutic modalities to manipulate the ALC/AMC ratio during R-CHOP cycles to improve DLBCL clinical outcomes.
机译:在弥漫性大B细胞淋巴瘤(DLBCL)诊断中,预后因素外周血绝对淋巴细胞/单核细胞比率(ALC / AMC)的局限性在于,它无法在治疗过程中顺序评估宿主/肿瘤微环境相互作用和临床结果。因此,我们研究了每个利妥昔单抗,环磷酰胺,阿霉素,长春新碱和泼尼松(R-CHOP)周期的ALC / AMC比率,以作为生存的预测指标。我们研究了107例被诊断为DLBCL的连续患者,仅接受R-CHOP治疗,然后在梅奥诊所就诊。无监督的分层聚类根据周期中ALC / AMC比率恢复的模式确定了四个聚类。在所有周期中,ALC / AMC比<1.1的簇中观察到的生存率最低。通过多变量分析,在所有周期中ALC / AMC比<1.1是总体生存期和无进展生存期的独立预测因素。 R-CHOP周期中的ALC / AMC比值可预测生存,并为开发治疗模式以在R-CHOP周期中操纵ALC / AMC比值以改善DLBCL临床结果提供平台。

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