首页> 外文期刊>Oncoimmunology. >CD163-positive tumor-associated macrophages and CD8-positive cytotoxic lymphocytes are powerful diagnostic markers for the therapeutic stratification of osteosarcoma patients: An immunohistochemical analysis of the biopsies fromthe French OS2006 phase 3 trial
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CD163-positive tumor-associated macrophages and CD8-positive cytotoxic lymphocytes are powerful diagnostic markers for the therapeutic stratification of osteosarcoma patients: An immunohistochemical analysis of the biopsies fromthe French OS2006 phase 3 trial

机译:CD163阳性肿瘤相关的巨噬细胞和CD8阳性细胞毒性淋巴细胞是骨肉瘤患者治疗分层的强大诊断标志:来自法国OS2006阶段3试验的活组织检查的免疫组化分析

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The French phase 3 trial (OS 2006) testing zoledronic acid, an osteoclast inhibitor, with chemotherapy and surgery did not improve the outcome of patients with osteosarcoma (OS). To understand this unexpected result, the presence of infiltrating immune cells was investigated in 124 pre-therapeutic biopsies of patients enrolled in the trial. The percentage of CD68/CD163 tumor-infiltrating macrophages (TAMs), CD8(+) lymphocytes, osteoclasts, and the PD1/PDL-1 checkpoint were assessed by immunohistochemistry. M1/M2 macrophage polarization was characterized by pSTAT1/CMAF staining. The expression of these biomarkers was correlated with clinical outcome. No statistical correlations were found with response to chemotherapy. High CD163 levels (>50% of cells per core; 43.8% of patients) were associated with CMAF nuclear expression and significantly correlated with better overall survival (p = 0.0025) and longer metastasis progression-free survival (MPFS, p = 0.0315) independently of metastatic status (p = 0.002). Only a trend was observed for patients with high CD68-positive cells (p = 0.0582). CD8(+) staining was positive in >50% of cases with a median staining of 1%. Lower CD8(+) levels were associated with metastatic disease at diagnosis and the presence of CD8-positive cells significantly correlated with improved overall survival in zoledronate-treated patients (p = 0.0415). PD1/PDL-1 staining was negative in >80% of cases and was not correlated with outcome. Finally, CD163-positive TAMs and CD8 positive cells are crucial prognostic biomarkers in OS, whereas PD1/PDL-1 checkpoint plays a minor role. For the first time, we described a correlation between CD8 positive cells and survival in zoledronate-treated patients. The immunohistochemical analysis of the microenvironment in biopsies may represent a novel tool for therapeutic stratification.
机译:法国第3阶段试验(OS 2006)测试唑妥酸,骨质体抑制剂,具有化疗和手术的疏松症抑制剂并未改善骨肉瘤患者的结果(OS)。要了解这种意外结果,研究了在患有试验中注册的124名患者的治疗性活组织检查中渗透渗透免疫细胞的存在。通过免疫组织化学评估CD68 / CD163肿瘤渗透巨噬细胞(TAMS),CD8(+)淋巴细胞,破骨细胞和PD1 / PDL-1检查点的百分比。 M1 / M2巨噬细胞极化的特征在于Pstat1 / CMAF染色。这些生物标志物的表达与临床结果相关。没有发现对化疗的反应没有统计相关性。高CD163水平(>每核的50%; 43.8%的患者)与CMAF核表达有关,与更好的整体存活(P = 0.0025)和更长的转移无进展存活(MPF,P = 0.0315)明显相关转移状态(p = 0.002)。对于高CD68阳性细胞患者仅观察到趋势(P = 0.0582)。 CD8(+)染色阳性> 50%的病例,中位数染色1%。降低CD8(+)水平与诊断中的转移性疾病有关,CD8阳性细胞的存在与唑妥替纳酸盐治疗的患者的改善总存活显着相关(P = 0.0415)。 PD1 / PDL-1染色在> 80%的病例中为阴性,并且与结果无关。最后,CD163阳性TAMS和CD8阳性细胞是OS中至关重要的预后生物标志物,而PD1 / PDL-1检查点起着次要作用。首次描述了CD8阳性细胞与唑妥替纳酸盐治疗患者的存活之间的相关性。在活组织检查中的微环境的免疫组化分析可以代表一种用于治疗分层的新型工具。

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