首页> 美国卫生研究院文献>Oncotarget >Radiotherapy prolongs the survival of advanced non-small-cell lung cancer patients undergone to an immune-modulating treatment with dose-fractioned cisplatin and metronomic etoposide and bevacizumab (mPEBev)
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Radiotherapy prolongs the survival of advanced non-small-cell lung cancer patients undergone to an immune-modulating treatment with dose-fractioned cisplatin and metronomic etoposide and bevacizumab (mPEBev)

机译:放射疗法可延长接受剂量分级顺铂节律性依托泊苷和贝伐单抗(mPEBev)免疫调节治疗的晚期非小细胞肺癌患者的生存期

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摘要

Radiotherapy (RT), together with a direct cytolytic effect on tumor tissue, also elicits systemic immunological events, which sometimes result in the regression of distant metastases (abscopal effect). We have shown the safety and anti-tumor activity of a novel metronomic chemotherapy (mCH) regimen with dose-fractioned cisplatin, oral etoposide and bevacizumab, a mAb against the vasculo-endothelial-growth-factor (mPEBev regimen), in metastatic non-small-cell-lung cancer (mNSCLC). This regimen, designed on the results of translational studies, showed immune-modulating effects that could trigger and empower the immunological effects associated with tumor irradiation. In order to assess this, we carried out a retrospective analysis in a subset of 69 consecutive patients who received the mPEBev regimen within the BEVA2007 trial. Forty-five of these patients, also received palliative RT of one or more metastatic sites. Statistical analysis (a Log-rank test) revealed a much longer median survival in the group of patients who received RT [mCH vs mCH + RT: 12.1 +/-2.5 (95%CI 3.35-8.6) vs 22.12 +/-4.3 (95%CI 11.9-26.087) months; P=0.015] with no difference in progression-free survival. In particular, their survival correlated with the mPEBev regimen ability to induce the percentage of activated dendritic cells (DCs) (CD3-CD11b+CD15-CD83+CD80+) [Fold to baseline value (FBV) ≤1 vs >1: 4+/-5.389 (95%CI,0- 14.56) vs 56+/-23.05 (95%CI,10.8-101.2) months; P:0.049)] and central-memory- T-cells (CD3+CD8+CD45RA-CCR7+) [FBV ≤ 1 vs >1: 8+/-5.96 (95%CI,0-19.68) vs 31+/-12.3 (95%CI,6.94-55.1) months; P:0.045].These results suggest that tumor irradiation may prolong the survival of NSCLC patients undergone mPEBev regimen presumably by eliciting an immune-mediated effect and provide the rationale for further perspective clinical studies.
机译:放射疗法(RT)加上对肿瘤组织的直接细胞溶解作用,还会引发全身性免疫事件,有时会导致远处转移的消退(远隔效应)。我们已经显示了一种新型的节律化疗(mCH)方案,在剂量级分的顺铂,口服依托泊苷和贝伐单抗(一种对抗血管内皮生长因子的单抗)中的安全性和抗肿瘤活性,在转移性非小细胞肺癌(mNSCLC)。根据转化研究的结果设计的该方案显示出免疫调节作用,可以触发并增强与肿瘤照射相关的免疫学作用。为了对此进行评估,我们对BEVA2007试验中接受mPEBev方案的69位连续患者的亚组进行了回顾性分析。这些患者中有四十五名也接受了一个或多个转移部位的姑息性放疗。统计分析(对数秩检验)显示,接受RT的患者组中位生存期更长[mCH vs mCH + RT:12.1 +/- 2.5(95%CI 3.35-8.6)vs 22.12 +/- 4.3( 95%CI 11.9-26.087)个月; P = 0.015],无进展生存期无差异。特别是,它们的存活率与mPEBev方案诱导活化树突状细胞(DC)(CD3-CD11b + CD15-CD83 + CD80 +)百分比的能力有关[折叠至基线值(FBV)≤1vs> 1:4 + / -5.389(95%CI,0- 14.56)个月与56 +/- 23.05(95%CI,10.8-101.2)个月; P:0.049)和中央记忆T细胞(CD3 + CD8 + CD45RA-CCR7 +)[FBV≤1 vs> 1:8 +/- 5.96(95%CI,0-19.68)vs 31 +/- 12.3 (95%CI,6.94-55.1)个月; [P:0.045]。这些结果提示,肿瘤照射可能通过引起免疫介导的作用而延长了接受mPEBev方案的NSCLC患者的生存期,并为进一步的临床研究提供了依据。

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