Department of Pre-clinical Dentistry, Health Sciences Faculty, Universidad Europea de Madrid, Villaviciosa de Odón, Madrid 28670, Spain.
Department of Health Sciences, Health Sciences Faculty, Universidad Europea de Madrid, Villaviciosa de Odón, Madrid 28670, Spain.
World J Gastroenterol. 2020 Apr 28;26(16):1979-1986. doi: 10.3748/wjg.v26.i16.1979.
In metastatic colorectal cancer (mCRC), the anti-vascular endothelial growth factor drug bevacizumab (BVZ) plus chemotherapy significantly improves progression-free survival compared to chemotherapy (CT) alone. This benefit is not, however, observed in all patients. While increased chemokine gene expression promoting angiogenesis has been proposed as a prognostic mCRC biomarker, few studies have examined its relationship with drug efficacy. This study sought to analyze tumor gene expression in six patients with different efficacy of BVZ-containing CT in terms of the tumor response to treatment.
We report six cases of stage IV KRAS-mutated mCRC. Patients were given first line treatment with BVZ-containing chemotherapy in University Hospital of Fuenlabrada. The six patients differed in terms of primary tumor location (right/left side), tumor burden (mostly hepatic and peritoneal disease) and clinical disease course. Before treatment onset, total RNA was isolated from paraffinated tumor biopsy specimens and gene expression quantified through conventional RT-qPCR procedures. Our main finding was that expression levels were several times higher in three patients with lower progression free survival (under 6 mo) from the start of treatment.
A higher expression of was observed in the three patients showing worse tumor response to treatment.
在转移性结直肠癌(mCRC)中,抗血管内皮生长因子药物贝伐珠单抗(BVZ)联合化疗与单独化疗相比,显著提高了无进展生存期。然而,并非所有患者都能观察到这种获益。虽然促血管生成的趋化因子基因表达增加已被提出作为 mCRC 的预后生物标志物,但很少有研究探讨其与药物疗效的关系。本研究旨在分析六位接受含 BVZ 的 CT 治疗的 mCRC 患者的肿瘤基因表达,这些患者对治疗的肿瘤反应存在差异。
我们报告了六例 KRAS 突变的 IV 期 mCRC 患者。患者在富恩拉夫拉达大学医院接受了含 BVZ 的一线化疗治疗。这六位患者在原发肿瘤位置(右侧/左侧)、肿瘤负荷(主要为肝和腹膜疾病)和临床疾病过程方面存在差异。在治疗开始前,从石蜡包埋的肿瘤活检标本中分离总 RNA,并通过常规 RT-qPCR 程序定量基因表达。我们的主要发现是,在从治疗开始起无进展生存期(<6 个月)较短的三位患者中,表达水平高出数倍。
在肿瘤对治疗反应较差的三位患者中观察到 表达水平较高。