首页> 外文期刊>Annals of surgical oncology >High serum levels of vascular endothelial growth Factor-A and transforming growth factor-β1 before neoadjuvant chemoradiotherapy predict poor outcomes in patients with esophageal squamous cell carcinoma receiving combined modality therapy
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High serum levels of vascular endothelial growth Factor-A and transforming growth factor-β1 before neoadjuvant chemoradiotherapy predict poor outcomes in patients with esophageal squamous cell carcinoma receiving combined modality therapy

机译:新辅助放化疗前血管内皮生长因子 A 和转化生长因子 β1 血清水平高,可预测接受联合治疗的食管鳞状细胞癌患者预后不佳

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Background and Purpose: This study was aimed at using proximity ligation assay (PLA) followed by enzyme-linked immunosorbent assay (ELISA) to identify serum biomarkers that predict treatment response and survival for patients with esophageal squamous cell carcinoma (ESCC) undergoing neoadjuvant concurrent chemoradiotherapy (CCRT) followed by esophagectomy. Methods: Seventy-nine patients with ESCC receiving CCRT of taxane-based/5-fluorouracil-based chemotherapy and 40 Gy followed by surgery were enrolled. Serum samples were collected before and <1 month after CCRT. Fifteen biomarkers were analyzed using PLA. Biomarkers significantly correlating with pathological response/survival were verified by ELISA. Associations of the serum level of biomarkers and clinical factors with pathological response, disease-free survival (DFS), and overall survival (OS) were evaluated by analysis of variance and log-rank tests. Results: Thirty patients had complete response (38 ), 37 had microscopic residual disease (47 ), and 12 had macroscopic residual disease (15 ). With a median follow-up of 52.8 months, the median DFS was 43 months. Among the 15 biomarkers screened by PLA, vascular endothelial growth factor (VEGF)-A and transforming growth factor (TGF)-β1 were significantly associated with pathological response and/or DFS. These biomarkers were further analyzed by ELISA to confirm initial biomarker findings by PLA. After ELISA of these two markers, only VEGF-A levels were significantly correlated with pathological response. On multivariate analysis, patients with combined high pre-CCRT VEGF-A and TGF-β1 levels (greater than or equal to the median), independent of pathological response, had significantly worse DFS (11 months vs. median not reached; p = 0.007) and OS (16 vs. 46 months; p = 0.07). Conclusions: Pre-CCRT serum VEGF-A and TGF-β1 levels may be used to predict pathological response and survivals for ESCC patients receiving combined-modality therapy.
机译:背景和目的:本研究旨在使用邻近结扎试验 (PLA) 和酶联免疫吸附试验 (ELISA) 来鉴定预测食管鳞状细胞癌 (ESCC) 患者接受新辅助同步放化疗 (CCRT) 和食管切除术的治疗反应和生存率的血清生物标志物。方法:选取79例接受紫杉烷类/5-氟尿嘧啶化疗CCRT和40 Gy术后手术的ESCC患者。在 CCRT 之前和 <后 1 个月收集血清样本。使用PLA分析了15种生物标志物。通过ELISA验证与病理反应/生存显著相关的生物标志物。通过方差分析和对数秩检验评估血清生物标志物水平和临床因素与病理反应、无病生存期 (DFS) 和总生存期 (OS) 的关联。结果:30例患者完全缓解(38%),37例患者有显微镜下残留病灶(47%),12例患者有肉眼下残留病灶(15%)。中位随访时间为52.8个月,中位DFS为43个月。在PLA筛选的15种生物标志物中,血管内皮生长因子(VEGF)-A和转化生长因子(TGF)-β1与病理反应和/或DFS显著相关。通过ELISA进一步分析这些生物标志物,以确认PLA的初步生物标志物发现。对这两种标志物进行ELISA检测后,只有VEGF-A水平与病理反应显著相关。在多变量分析中,CCRT 前 VEGF-A 和 TGF-β1 水平(大于或等于中位数)联合较高的患者(大于或等于中位数)与病理反应无关,DFS 显著更差(11 个月 vs 未达到中位数;p = 0.007)和 OS(16 个月 vs. 46 个月;p = 0.07)。结论:CCRT前血清VEGF-A和TGF-β1水平可用于预测接受联合治疗的ESCC患者的病理反应和生存率。

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  • 来源
    《Annals of surgical oncology》 |2014年第7期|2361-2368|共8页
  • 作者单位

    Department of Radiation Oncology, Stanford University, Stanford, CA, United States, Division of;

    Department of Radiation Oncology, Stanford University, Stanford, CA, United States;

    Division of Radiation Oncology, Department of Oncology, National Taiwan University Hospital, TaipeiDepartment of Surgery, National Taiwan University Hospital, Taipei, Taiwan;

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  • 原文格式 PDF
  • 正文语种 英语
  • 中图分类 外科学;
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