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首页> 外文期刊>The oncologist >Genomic Profiling of HER2‐Positive Gastric Cancer: PI3K/Akt/mTOR Pathway as Predictor of Outcomes in HER2‐Positive Advanced Gastric Cancer Treated with Trastuzumab
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Genomic Profiling of HER2‐Positive Gastric Cancer: PI3K/Akt/mTOR Pathway as Predictor of Outcomes in HER2‐Positive Advanced Gastric Cancer Treated with Trastuzumab

机译:HER2阳性胃癌的基因组分析:PI3K / AKT / MTOR途径作为曲妥珠单抗治疗HER2阳性晚期胃癌的结果预测因子

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Abstract Background HER2‐positive gastric cancer (GC) affects 7%–34% of patients with GC. Trastuzumab‐based first‐line treatment has become the standard of care for HER2‐positive advanced gastric cancer (AGC). However, there are no clinically validated biomarkers for resistance to HER2‐targeted therapies. Upregulation of PI3K pathway and tyrosine kinase receptor (TKR) alterations have been noted as molecular mechanisms of resistance in breast cancer. Our study aimed to perform a molecular characterization of HER2‐positive AGC and investigate the role of PI3K/Akt/mTOR signaling pathway activation and TKR gene copy number (GCN) gains as predictive biomarkers in HER2‐positive AGC treated with trastuzumab. Patients and Methods Forty‐two HER2‐positive GC samples from patients treated with trastuzumab‐based first‐line chemotherapy were selected. DNA samples were sequenced. PTEN and MET immunohistochemistry were also performed. Results Concurrent genetic alterations were detected in 97.1% of HER2‐positive AGC. We found activation of PI3K/Akt/mTOR pathway in 52.4% of patients and TKR GCN gains in 38.1%. TKR GCN gains did not correlate with overall survival (OS) or progression‐free survival (PFS). Multivariate Cox models showed that PI3K/Akt/mTOR activation negatively affects the effectiveness of trastuzumab‐based chemotherapy in terms of OS and PFS. Conclusion Our results provide for the first time a detailed molecular profile of concurrent genetic alterations in HER2‐positive AGC. PI3K pathway activation could be used as a predictive marker of worse outcome in this patient population. In addition, gains in copy number of other TKR genes in this subgroup may also influence the survival benefit obtained with trastuzumab. Implications for Practice This article reports, for the first time, a detailed molecular profile of genomic alterations in patients with HER2‐positive advanced gastric cancer (AGC). PI3K/Akt/mTOR signaling pathway activation seems to have a differentially negative effect on overall survival and progression‐free survival in AGC treated with trastuzumab‐based chemotherapy. Combining different targeted agents could be a successful therapeutic strategy to improve the prognosis of HER2‐positive AGC.
机译:摘要背景Her2阳性胃癌(GC)影响GC患者的7%-34%。基于Trastuzumab的一线治疗已成为HER2阳性晚期胃癌(AGC)的护理标准。然而,没有临床验证的生物标志物,用于抵抗Her2靶向疗法。 PI3K途径的上调和酪氨酸激酶受体(TKR)改变已被指出作为乳腺癌抗性的分子机制。我们的研究旨在进行HER2阳性AGC的分子表征,并研究PI3K / AKT / MTOR信号传导途径激活和TKR基因拷贝数(GCN)在用曲妥珠单抗处理的HER2阳性AGC中获得预测生物标志物的作用。选择患者和方法从患有基于曲妥珠单抗的一线化疗治疗的患者的42例HER2阳性GC样本。测序DNA样品。也进行了PTEN并达到了免疫组织化学。结果在97.1%的HER2阳性AGC中检测到并发遗传改变。我们发现52.4%的患者和TKR GCN患者的PI3K / AKT / MTOR途径的激活,38.1%。 TKR GCN增益与整体存活(OS)或无进展生存(PFS)不相关。多元COX模型表明,PI3K / AKT / MTOR活化对OS和PFS方面的曲妥珠木疗法的有效性产生负面影响。结论我们的结果首次提供HER2阳性AGC中同时遗传改变的详细分子谱。 PI3K途径激活可以用作该患者群体中更糟糕的结果的预测标记。此外,该亚组中其他TKR基因的拷贝数的增加也可能影响用曲妥珠单抗获得的存活益处。对实践本文的影响是,首次报告了Her2阳性晚期胃癌(AGC)的基因组改变的详细分子谱。 PI3K / AKT / MTOR信号通路活化似乎对AGC的整体存活和无进展存活似乎具有差异差异的负面影响,所述AGC治疗基于曲妥珠猴的化疗治疗。结合不同的靶向药物可能是提高HER2阳性AGC预后的成功治疗策略。

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