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首页> 外文期刊>Cancer science. >Baseline carcinoembryonic antigen (CEA) serum levels predict bevacizumab-based treatment response in metastatic colorectal cancer
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Baseline carcinoembryonic antigen (CEA) serum levels predict bevacizumab-based treatment response in metastatic colorectal cancer

机译:基线癌胚抗原(CEA)血清水平预测转移性结直肠癌中基于贝伐单抗的治疗反应

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Carcinoembryonic antigen (CEA) affects tumorigenesis by enhancing tumor cell survival and by inducing tumor angiogenesis. This study aimed to evaluate baseline CEA serum levels to predict bevacizumab-based therapy effect and survival in patients with metastatic colorectal cancer (mCRC). Two hundred and ninety eight mCRC patients receiving chemotherapy plus either bevacizumab or cetuximab were analyzed in a retrospective study. Disease control (DC), progression-free survival (PFS), and overall survival were assessed and related to pretreatment CEA serum levels. Patients with baseline CEA serum levels below the statistical median of 26.8ng/mL (group I) were compared with patients with higher CEA levels (group II). The cetuximab-based treatment cohort was analyzed for specificity assessment of CEA to predict the anti-vascular endothelial growth factor effect in mCRC. Baseline CEA serum levels inversely correlated with therapeutic response in patients receiving bevacizumab-based treatment (disease control rate, 84% vs 60%), inversely correlated with median PFS leading to a median PFS benefit of 2.1months for patients in group I when compared with group II, as well as inversely correlated with median overall survival (37.5months vs 21.4months). In an independent cohort of 129 patients treated with cetuximab-based therapy, no association of therapeutic response or PFS with CEA serum levels was found. As expected, baseline CEA levels were prognostic for mCRC. These data give first evidence that baseline serum CEA levels might constitute an important predictor for the efficacy of first-line bevacizumab-based therapy in patients with mCRC.
机译:癌胚抗原(CEA)通过增强肿瘤细胞存活率和诱导肿瘤血管生成来影响肿瘤发生。这项研究旨在评估基线CEA血清水平,以预测基于贝伐单抗的治疗效果和转移性结直肠癌(mCRC)患者的生存率。在一项回顾性研究中分析了298例接受化疗加贝伐单抗或西妥昔单抗治疗的mCRC患者。评估疾病控制(DC),无进展生存期(PFS)和总生存期,并与治疗前CEA血清水平相关。将基线CEA血清水平低于统计中位数26.8ng / mL的患者(I组)与较高CEA水平的患者(II组)进行比较。分析了基于西妥昔单抗的治疗队列对CEA的特异性评估,以预测mCRC中的抗血管内皮生长因子作用。与接受贝伐单抗治疗的患者相比,基线CEA血清水平与治疗反应呈负相关(疾病控制率,分别为84%和60%),与中位PFS呈负相关,与I组相比,中位PFS获益为2.1个月第二组,与中位总体生存率(37.5个月对21.4个月)成反比。在以西妥昔单抗为基础治疗的129名患者的独立队列中,未发现治疗反应或PFS与CEA血清水平相关。正如预期的那样,基线CEA水平可预测mCRC。这些数据首次证明基线血清CEA水平可能构成基于贝伐单抗的一线治疗对mCRC患者疗效的重要预测指标。

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