中东结直肠癌患者KRAS突变的频率和临床影响

J. Zekri, S. Karim, A. Al-Shehri, M. Mahrous, T. Darwish, H. E. Taani
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引用次数: 2

摘要

背景:结直肠癌(CRC)是世界范围内和中东地区(ME)重大的医疗负担。KRAS突变在晚期结直肠癌治疗中对表皮生长因子受体(EGFR)抑制剂产生耐药性。关于来自ME的KRAS突变率的数据是分散和稀缺的。我们的目标是收集和回顾所有评估来自ME的CRC患者KRAS突变频率的大规模研究。方法:使用关键词KRAS、K-ras、结直肠癌、Middle East以及ME国家名称进行Pubmed和谷歌Scholar检索。超过90名患者的研究被纳入该综述。结果:11项研究纳入了90多例患者。在所有11项研究中,KRAS突变率从13%到56%不等。五项研究单独或作为亚组分析的一部分报道了M1期KRAS突变率。在这些研究中,在8-45%的病例中发现了突变。KRAS突变分别在3项、2项和1项研究中与女性、M1期和高CEA相关。结论:与ME不同的研究中报道的KRAS突变率存在广泛的变异性。这可能是由于研究中的患者数量较少以及缺乏KRAS突变的集中检测。为了确定KRAS突变率的准确性,需要在ME人群中进行更大规模和更协调的研究。
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Frequency and Clinical Impact of KRAS Mutations in Patients with Colorectal Cancer from the Middle East
Background : Colorectal cancer (CRC) is a significant healthcare burden worldwide and in the Middle East (ME). KRAS mutation confers resistance to epidermal growth factor receptor (EGFR) inhibitors in the treatment of advanced CRC. Data regarding the rate of KRAS mutation from the ME are scattered and scarce. We aim to collect and review all sizable studies evaluating the frequency of KRAS mutations in CRC patients from the ME. Method : A Pubmed and Google Scholar search was conducted using keywords including KRAS, K-ras, colorectal cancer and Middle East, along with names of each ME country. Studies including over 90 patients were included in the review. Result : Eleven studies containing more than 90 patients were identified. Among all eleven studies, KRAS mutation rate ranged from 13 to 56%. Five studies reported KRAS mutation rate in M1 stage either exclusively or as part of subgroup analysis. In these studies, mutations were found in 8-45% of cases. KRAS mutations were associated with female gender, M1 stage and high CEA in 3, 2, and 1 studies respectively. Conclusion : There is a broad range of variability in KRAS mutation rate reported in different studies from the ME. This may have been due to small number of patients in the studies and lack of centralized testing for KRAS mutations. Larger and more coordinated studies from the ME population are required to ascertain the accuracy of KRAS mutation rate.
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