Payandeh Mehrdad, Shazad Babak, Sadeghi Masoud, Shahbazi Maryam
Cancer Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran E-mail :
Asian Pac J Cancer Prev. 2016;17(4):1729-32. doi: 10.7314/apjcp.2016.17.4.1729.
In the patients with metastatic colorectal cancer (mCRC), RAS testing is the first step to identify those that could benefit from anti-EGFR therapy. This study examined associations between KRAS mutations and clinicopathological and survival data in Iranian patients with mCRC. Between 2008 to2015 in a retrospective study, 83 cases of mCRC were referred to the Clinic of Medical Oncology. The mean follow-up was 45 months that there were 27 deaths. The 3 patients that did not complete follow-up were censored from the study. KRAS and NRAS were analyzed using allele-specific PCR primers and pyrosequencing in exons 2, 3 and 4. Multivariate survival analysis using Cox's regression model was used for affecting of variables on overall survival (OS). The mean age at diagnosis for patients was 57.7 (range, 18 to 80 years) and 61.4% were male. There was no significant different between prognostic factors and KRAS mutation with wild-type. Also, There was no significant different between KRAS mutation and KRAS wild-type for survival, but there was a significant different between KRAS 12 and 13 mutations for survival (HR 0.13, 95% CI 0.03-0.66, P=0.01). In conclusion, the prevalence of KRAS mutations in CRC patients was below 50% but higher than in other studies in Iran. As in many studies, patients with KRAS 12 mutations had better OS thn those with KRAS 13 mutation. In addition to KRAS testing, other biomarkers are needed to determine the best treatment for patients with mCRC.
在转移性结直肠癌(mCRC)患者中,RAS检测是识别那些可能从抗表皮生长因子受体(EGFR)治疗中获益患者的第一步。本研究探讨了伊朗mCRC患者中KRAS突变与临床病理及生存数据之间的关联。在2008年至2015年的一项回顾性研究中,83例mCRC患者被转诊至肿瘤内科诊所。平均随访时间为45个月,有27例死亡。3例未完成随访的患者被排除在研究之外。使用等位基因特异性PCR引物和焦磷酸测序法对KRAS和NRAS的第2、3和4外显子进行分析。采用Cox回归模型进行多因素生存分析,以确定各变量对总生存期(OS)的影响。患者诊断时的平均年龄为57.7岁(范围为18至80岁),男性占61.4%。预后因素与KRAS突变型和野生型之间无显著差异。此外,KRAS突变型和野生型在生存率方面无显著差异,但KRAS第12和13位密码子突变在生存率方面存在显著差异(风险比0.13,95%可信区间0.03 - 0.66,P = 0.01)。总之,CRC患者中KRAS突变的发生率低于50%,但高于伊朗的其他研究。与许多研究一样,KRAS第12位密码子突变的患者总生存期优于KRAS第13位密码子突变的患者。除了KRAS检测外,还需要其他生物标志物来确定mCRC患者的最佳治疗方案。