脊髓灰质炎病毒可溶性受体在新诊断滤泡性淋巴瘤中的临床意义

IF 0.1 Q4 HEMATOLOGY
N. Nabih, A. Kamal, M. Naguib
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摘要

背景滤泡性淋巴瘤(FL)仍然是一种无法治愈的恶性肿瘤,其临床结果参差不齐,需要更好地了解疾病生物学。脊髓灰质炎病毒受体(PVR/CD155)在几种人类恶性肿瘤中显著过表达,具有独特的双重肿瘤免疫调节作用。然而,可溶性PVR(sCD155)在FL中的作用尚未完全阐明。方法采用夹心酶联免疫吸附法测定50例FL患者血清可溶性PVR(sCD155),并与20例健康对照组进行比较。此外,我们评估了它与这些患者的临床病理参数以及化疗反应的关系。结果FL患者的sCD155预处理水平显著高于对照组(P<0.001)。sCD155水平较高与侵袭性高风险临床病理参数有关,有B症状、晚期Ann Arbor III期和IV期、大体积疾病的FL患者的sCD155水平显著较高,和高危细胞遗传学(P值分别为0.01、0.048、0.028和<0.001)。此外,在50名患者中,24名(48%)患者在4-6个疗程的化疗(R-CHOP)后获得CR,26名(52%)患者没有缓解,sCD155水平较高与化疗反应不佳有关(P值<0.001)。应用受试者操作特征曲线。sCD155血清水平高于4.8 ng/ml是化疗不良反应的良好预测指标(曲线下面积:0.857,敏感性和特异性分别为88.46%和75%)。结论PVR(CD155)是一个潜在的治疗靶点,值得进一步研究,血清sCD155可作为治疗反应的生物标志物,用于预测FL的不良预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical significance of soluble form of poliovirus receptor in newly diagnosed follicular lymphoma
Background Follicular lymphoma (FL) remains an incurable malignancy with heterogeneous clinical outcomes that necessitate a better understanding of disease biology. Poliovirus receptor (PVR/CD155) is markedly overexpressed in several human malignant tumors and it has a unique dual oncoimmunoregulatory role. However, the role of the soluble form of PVR (sCD155) in FL has not been fully elucidated. Methods Soluble PVR(sCD155) were measured in the sera of 50 patients newly diagnosed with FL by sandwich enzyme-linked immunosorbent assay and compared with those of 20 healthy control participants. Moreover, we evaluated its association with the clinicopathological parameters as well as response to chemotherapy in such patients. Results Pretreatment level of sCD155 was significantly higher in patients with FL than in control participants (P<0.001). Higher levels of sCD155 were associated with aggressive high-risk clinicopathological parameters, sCD155 levels were significantly higher in FL patients with B symptoms, advanced Ann Arbor stage III and IV, bulky disease, and high-risk cytogenetic (P-value=0.01, 0.048, 0.028 and <0.001, respectively). In addition, of the 50 patients, 24 (48%) achieved CR after 4–6 courses of chemotherapy (R-CHOP), while 26 (52%) were not in remission, and higher levels of sCD155 were associated with poor response to chemotherapy (P-value<0.001). Receiver operating characteristic curve was applied. Serum level of sCD155 higher than 4.8 ng/ml is a good predictor for poor response to chemotherapy (area under the curve: 0.857, sensitivity and specificity 88.46% and 75%, respectively). Conclusion PVR (CD155) is a potential therapeutic target that warrants further investigations and serum sCD155 may be used as a biomarker of treatment response and for predicting poor outcome in FL.
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