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接受伊匹单抗治疗的IV期恶性黑色素瘤患者的治疗及反应的免疫相关性

Immunological correlates of treatment and response in stage IV malignant melanoma patients treated with Ipilimumab.

作者信息

Bjoern Jon, Juul Nitschke Nikolaj, Zeeberg Iversen Trine, Schmidt Henrik, Fode Kirsten, Svane Inge Marie

机构信息

Center for Cancer Immune Therapy, Herlev Hospital, University of Copenhagen, Herlev, Denmark; Department of Oncology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.

Center for Cancer Immune Therapy, Herlev Hospital, University of Copenhagen , Herlev, Denmark.

出版信息

Oncoimmunology. 2015 Nov 25;5(4):e1100788. doi: 10.1080/2162402X.2015.1100788. eCollection 2016 Apr.

Abstract

: Ipilimumab is effective in the treatment of metastatic malignant melanoma, but few biomarkers reliably predict treatment response. : Patients were treated with Ipilimumab for metastatic malignant melanoma. Blood and serum samples were collected before and during treatment. Mononuclear cells in peripheral blood were subjected to immune phenotypic analyses and cytokine levels were measured in serum samples. Results were correlated with clinical data. : A total of 40 patients were included in the analyses. Clinical response were associated with an increase after one series of treatment in absolute lymphocyte count (ALC) ( = 0.008), absolute T cell count ( = 0.02) and the absolute number of activated T cells in peripheral blood ( = 0.003). A high frequency of myeloid derived suppressor cells (MDSC) and a higher level of IL6 were associated with treatment failure, though not significantly. Levels of IL6 in serum above the median showed a tendency to associate with reduced survival by the 4th treatment series. Finally, treatment with Ipilimumab led to a decreased frequency of FOXP3+ regulatory T cells ( = 0.009). : Ipilimumab leads to increased ALC, T cell count and T cell activation in malignant melanoma patients responding to treatment. A high baseline frequency of myeloid-derived suppressor cells and high levels of IL6 is associated with a reduced chance of responding to therapy.

摘要

伊匹单抗在转移性恶性黑色素瘤的治疗中有效,但很少有生物标志物能可靠地预测治疗反应。患者接受伊匹单抗治疗转移性恶性黑色素瘤。在治疗前和治疗期间采集血液和血清样本。对外周血中的单核细胞进行免疫表型分析,并测定血清样本中的细胞因子水平。结果与临床数据相关。分析共纳入40例患者。临床反应与一系列治疗后绝对淋巴细胞计数(ALC)升高(P = 0.008)、绝对T细胞计数升高(P = 0.02)以及外周血中活化T细胞绝对数量升高(P = 0.003)相关。髓源性抑制细胞(MDSC)的高频率和较高水平的IL6与治疗失败相关,尽管不显著。血清中IL6水平高于中位数显示在第4个治疗周期时有生存降低的趋势。最后,伊匹单抗治疗导致FOXP3 +调节性T细胞频率降低(P = 0.009)。伊匹单抗使对治疗有反应的恶性黑色素瘤患者的ALC、T细胞计数和T细胞活化增加。髓源性抑制细胞的高基线频率和高水平的IL6与治疗反应机会降低相关。

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