期刊文献+

KRAS和BRCA1/2基因突变状态对卵巢上皮癌患者预后的影响 被引量:1

The effect of KRASand BRCA1/2 gene mutation status on the prognosis of patients with epithelial ovarian cancer
下载PDF
导出
摘要 目的探讨KRAS和BRCA1/2基因突变状态对评估卵巢上皮癌患者预后的临床价值。方法基因测序分析KRAS和BRCA1/2基因的多态性,采用Cox比例风险回归模型和Kaplan Meier生存分析法进行分析KRAS和BRCA1/2基因突变状态与化疗疗效及预后的相关性。结果 KRAS基因多态性与顺铂+紫杉醇化疗敏感性无相关性,对患者的无进展生存期及总生存期并不产生影响;与野生型BRCA2基因携带患者相比,BRCA1/2基因突变患者对顺铂+紫杉醇化疗相对较好的反应性,有望获得相对较好的生存期。结论BRCA1/2基因突变状态预示对顺铂+紫杉醇化疗相对敏感,患者能获得相对较好的生存期,BRCA1/2基因有可能作为一种生物标记物指导卵巢上皮癌的个性化化疗。 [Objective ] To investigate the clinic;d valueof KRAS and BRCA1/2 gene mutation status in assessing the prognosis of patients with epithelial ovarian cancer. [Methods] The polymorphism of KRAS and BRCA1/2 gene sequencing was studied using Cox proportional hazards regression model and Kaplan Meier survival analysis method was used to analyzethe correlation between KRAS and BRCA1/2 gene mutation status and chemotherapy efficacy and prognosis. [ Results ] There was no correlatior between the KRAS gene polymorphism and susceptibility to cis- platin plus paclitaxel chemotherapy, which did not affect the progression free survival and overall survival of pa- tients; Compared with the wild type BRCA2 gene patients carried, BRCA1/2 gene mutation in patients with cisplatin plus paclitaxel chemotherapy were in relatively good re-activity, who was expected to be relatively good survival. [Conclusion] BRCA1/2 gene mutations that are relatively sensitive to cisplatin plus paclitaxel chemotherapy, pa- tients can get relatively good survival, BRCA1/2 gene may serve as a biomarker for individualized chemotherapy guidance of epithelial ovarian cancer.
出处 《中国现代医学杂志》 CAS CSCD 北大核心 2014年第22期31-34,共4页 China Journal of Modern Medicine
关键词 KRAS BRCA1 2 卵巢上皮癌 预后 KRAS BRCA1/2 epithelial ovarian cancer prognosis
  • 相关文献

参考文献24

  • 1HIGGINS MJ, BASELGA J. Targeted therapies for breast cancer [J]. The Journal of Clinical Investigation, 2011, 121(10): 3797- 3803.
  • 2HANAHAN D, WEINBERG RA. The hallmarks of eaneer[J]. Cell, 2000, 100(1): 57-70.
  • 3ARDIGHIERI L, ZEPPERNICK F, HANNIBAL CG, et al. Muta- tional analysis of BRAF and KRAS in ovarian serous borderline (atypical proliferative) tumours and associated peritoneal implants [J]. The Journal of Pathology, 2014, 232(1): 16-22.
  • 4REUTER CWM, MORGAN MA, BERGMANN L. Targeting the Ras signaling pathway: a rational, mechanism-based treatment for hematologic malignancies[J]. Blood, 2000, 96(5): 1655-1669.
  • 5KING MC, MARKS JH, MANDELL JB. Breast and ovarian can- cer risks due to inherited mutations in BRCA1 and BRCA2[J]. Scienee, 2003, 302(5645): 643-646.
  • 6BROHET RM, VELTHUIZEN ME, HOGERVORST FBL, et al. Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BR- CA2 Dutch founder mutations[J]. Journal of Medical C:netics, 2014, 51(2): 98-107.
  • 7BOLTON KL, CHENEVIX-TRENCH G, GOH C, et at. Associa- tion between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer[J]. Jama, 2012, 307 (4): 382-389.
  • 8Cancer Genome Atlas Research Network. Inte graled genomic analyses of ovarian carcinoma[J]. Nature, 2011, 474(7353): 609- 615.
  • 9GALLAGHER D J, KONNER JA, BELL-MCGUINN KM, et al. Survival in epithelial ovarian cancer: a multivariate analysis in- corporating BRCA mutalion status and platinum sensitivity [J]. Annals of Oneology, 2011, 22(5): 1127-1132.
  • 10KRIVAK TC, DARCY KM, TIAN C, et al. Relationship be- tween ERCC1 polymorphisms, disease progression, and survival in the Gynecologic Oncology Group Phase 1I Trim of intraperi- toneal versus intravenous cisplatin and paclitaxel for stage m epithelial ovarian cancer[J]. Journal of Clinical Oncology, 2008, 26(21): 3598-3606.

同被引文献13

  • 1Jung KW, Won YJ, Kong HJ, et al. Cancer statistics in incidence, mortality, survival and prevalence in 2010[J]. Research and Treatment, 2013, 45(1): 1-14.
  • 2Siegel R, Desantis C, Jemal A. Colorectal cancer statistics, Korea: Cancer 2014[J].CA, 2014, 64(2): 104-117.
  • 3Demes M, Seheil-Bertram S, Bartseh H, et al. Signature of mi- erosatellite instability, KRAS and BRAF gene mutations in Ger- man patients with locally advanced rectal adenoeareinoma before and after neoadjuvant 5-FU radioehemotherapy[J]. Journal of Gastrointestinal Oneology, 2013, 4(2): 182-192.
  • 4Southward K, Hutehins G, Handley K, et al. K-ras mutation is a negative prognostic marker, and does not preclude benefit from 5-fu in stage l]/m eoloreetal cancer[C]. Journal of Pathology, 2011, 224: $4.
  • 5National Cancer Institute. Common Terminology Criteria for Ad- verse Events (CTCAE) Version 4.02[S/OL]. (2009-09-15) [2011- 12-30].
  • 6Schubbert S, Shannon K, Bollag G. Hyperactive ras in develop mental disorders and cancer[J]. Nature Reviews Cancer, 2007, 7(4): 295-308.
  • 7Etienne-Grimaldi MC, Formento JL, Franeoual M, et al. K-Ras mutations and treatment outcome in eolorectal cancer patients re- ceiving exclusive fluoropyrimidine therapy[J]. Clinical Cancer Re- search, 2008, 14(15): 4830-4835.
  • 8Carsten B, Igor B, Anatoly M, et al. Fluorouracil, leucovorin, and oxaliplatin with and without eetuximab in the first-line treatment of metastatic eoloreetal cancer[J]. Journal of Clinical Ontology, 2009, 27(5): 663-671.
  • 9Li M, Liang Z, Sun X, et al. A polymeric prodrug of 5-fluo- rouracil-l-acetic acid using a multi-hydroxyl polyethylene glycol derivative as the drug carrier[J]. PLoS One, 2014, 9(11): e112888.
  • 10Mori K, Hasegawa M, Nishida M, et al. Expression levels of thymidine phosphorylase and dihydropyrimidine dehydrogenase in various human tumor tissues[J]. International Journal of Oncology, 2000, 17(1): 33-41.

引证文献1

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部