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本文引用的文献

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Clinicopathological characteristics and prognostic impact of colorectal cancers with NRAS mutations.NRAS 突变型结直肠癌的临床病理特征及预后影响
Oncol Rep. 2014 Jul;32(1):50-6. doi: 10.3892/or.2014.3165. Epub 2014 May 6.
2
BRAF mutation is associated with distinct clinicopathological characteristics in colorectal cancer: a systematic review and meta-analysis.BRAF 突变与结直肠癌的独特临床病理特征相关:系统评价和荟萃分析。
Colorectal Dis. 2013 Dec;15(12):e711-8. doi: 10.1111/codi.12427.
3
KRAS mutational status in Japanese patients with colorectal cancer: results from a nationwide, multicenter, cross-sectional study.日本结直肠癌患者 KRAS 基因突变状态:一项全国性、多中心、横断面研究的结果。
Jpn J Clin Oncol. 2013 Jul;43(7):706-12. doi: 10.1093/jjco/hyt062. Epub 2013 May 8.
4
Prognostic relevance of KRAS and BRAF mutations in Japanese patients with colorectal cancer.结直肠癌日本患者 KRAS 和 BRAF 突变的预后相关性。
Int J Clin Oncol. 2013 Dec;18(6):1042-8. doi: 10.1007/s10147-012-0501-x. Epub 2012 Nov 29.
5
The prognostic value of BRAF mutation in colorectal cancer and melanoma: a systematic review and meta-analysis.BRAF 突变在结直肠癌和黑色素瘤中的预后价值:系统评价和荟萃分析。
PLoS One. 2012;7(10):e47054. doi: 10.1371/journal.pone.0047054. Epub 2012 Oct 9.
6
Effect of oxaliplatin, fluorouracil, and leucovorin with or without cetuximab on survival among patients with resected stage III colon cancer: a randomized trial.奥沙利铂、氟尿嘧啶和亚叶酸联合或不联合西妥昔单抗治疗可切除的 III 期结肠癌患者的生存影响:一项随机试验。
JAMA. 2012 Apr 4;307(13):1383-93. doi: 10.1001/jama.2012.385.
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Predictive and prognostic roles of BRAF mutation in stage III colon cancer: results from intergroup trial CALGB 89803.BRAF 突变在 III 期结肠癌中的预测和预后作用:CALGB 89803 组间试验的结果。
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8
Molecular profile and copy number analysis of sporadic colorectal cancer in Taiwan.台湾散发性结直肠癌的分子谱和拷贝数分析。
J Biomed Sci. 2011 Jun 7;18(1):36. doi: 10.1186/1423-0127-18-36.
9
DNA mismatch repair status and colon cancer recurrence and survival in clinical trials of 5-fluorouracil-based adjuvant therapy.基于氟尿嘧啶的辅助治疗临床试验中 DNA 错配修复状态与结肠癌复发和生存的关系。
J Natl Cancer Inst. 2011 Jun 8;103(11):863-75. doi: 10.1093/jnci/djr153. Epub 2011 May 19.
10
Mutations in BRAF correlate with poor survival of colorectal cancers in Chinese population.在中国人群中,BRAF 突变与结直肠癌患者的不良预后相关。
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KRAS和BRAF突变在根治性切除的结直肠癌中的预后价值。

Prognostic value of KRAS and BRAF mutations in curatively resected colorectal cancer.

作者信息

Kadowaki Shigenori, Kakuta Miho, Takahashi Shuhei, Takahashi Akemi, Arai Yoshiko, Nishimura Yoji, Yatsuoka Toshimasa, Ooki Akira, Yamaguchi Kensei, Matsuo Keitaro, Muro Kei, Akagi Kiwamu

机构信息

Shigenori Kadowaki, Akira Ooki, Kensei Yamaguchi, Division of Gastroenterology, Saitama Cancer Center, Saitama 362-0806, Japan.

出版信息

World J Gastroenterol. 2015 Jan 28;21(4):1275-83. doi: 10.3748/wjg.v21.i4.1275.

DOI:10.3748/wjg.v21.i4.1275
PMID:25632202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4306173/
Abstract

AIM

To investigate the prognostic role of KRAS and BRAF mutations after adjustment for microsatellite instability (MSI) status in Japanese colorectal cancer (CRC) population.

METHODS

We assessed KRAS and BRAF mutations and MSI status in 813 Japanese patients with curatively resected, stage I-III CRC and examined associations of these mutations with disease-free survival (DFS) and overall survival (OS) using uni- and multivariate Cox proportional hazards models.

RESULTS

KRAS and BRAF mutations were detected in 312 (38%) of 812 and 40 (5%) of 811 tumors, respectively. KRAS mutations occurred more frequently in females than in males (P=0.02), while the presence of BRAF mutations was significantly associated with the female gender (P=0.006), proximal tumor location (P<0.001), mucinous or poorly differentiated histology (P<0.001), and MSI-high tumors (P<0.001). After adjusting for relevant variables, including MSI status, KRAS mutations were associated with poorer DFS (HR=1.35; 95%CI: 1.03-1.75) and OS (HR=1.46; 95%CI: 1.09-1.97). BRAF mutations were poor prognostic factors for DFS (HR=2.20; 95%CI: 1.19-4.06) and OS (HR=2.30; 95%CI: 1.15-4.71). Neither the BRAF by MSI interaction test nor the KRAS by MSI interaction test yielded statistically significant results for DFS and OS.

CONCLUSION

KRAS and BRAF mutations are associated with inferior survival, independent of MSI status, in Japanese patients with curatively resected CRC.

摘要

目的

在日本结直肠癌(CRC)人群中,研究校正微卫星不稳定性(MSI)状态后KRAS和BRAF突变的预后作用。

方法

我们评估了813例接受根治性切除的Ⅰ-Ⅲ期日本CRC患者的KRAS和BRAF突变以及MSI状态,并使用单因素和多因素Cox比例风险模型检查这些突变与无病生存期(DFS)和总生存期(OS)的相关性。

结果

在812例肿瘤中的312例(38%)和811例肿瘤中的40例(5%)中分别检测到KRAS和BRAF突变。KRAS突变在女性中比在男性中更频繁发生(P=0.02),而BRAF突变的存在与女性性别(P=0.006)、肿瘤近端位置(P<0.001)、黏液性或低分化组织学(P<0.001)以及MSI高的肿瘤(P<0.001)显著相关。在校正包括MSI状态在内的相关变量后,KRAS突变与较差的DFS(HR=1.35;95%CI:1.03-1.75)和OS(HR=1.46;95%CI:1.09-1.97)相关。BRAF突变是DFS(HR=2.20;95%CI:1.19-4.06)和OS(HR=2.30;95%CI:1.15-4.71)的不良预后因素。BRAF与MSI的相互作用试验以及KRAS与MSI的相互作用试验在DFS和OS方面均未产生具有统计学意义的结果。

结论

在接受根治性切除的日本CRC患者中,KRAS和BRAF突变与较差的生存率相关,且与MSI状态无关。