CN108070651A - 一种评估crc复发风险的诊断分析/预后分析方法 - Google Patents
一种评估crc复发风险的诊断分析/预后分析方法 Download PDFInfo
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Abstract
一种评估CRC复发风险的诊断分析/预后分析方法,包括FGF18纤维母细胞生长因子18,PGR孕酮受体,ERBB2 v‑erb‑b2成红细胞的白血病病毒性致癌基因同系物2,神经/恶性胶质瘤衍生的致癌基因同系物(禽鸟),MKI67增殖标记Ki‑67,BCL2 B‑细胞慢性淋巴细胞性白血病/淋巴瘤2,INHBA人类抑制素,beta A。本发明精确地判定活组织检查或者手术切除的肿瘤组织是否的确是结肠直肠癌,以及哪些患者癌症复发的几率高,然后根据判定结果选择根据患者肿瘤基因构造量身定制最有效的方案进行化学疗法。
Description
本发明涉及医疗评估方面,尤其涉及一种评估CRC复发风险的诊断分析/预后分析方法。
背景技术
直肠结肠癌(简称CRC)是最常见的恶性肿瘤之一,全世界每年新增120万新病例,每年约有70万人死亡。在发达国家CRC的死亡率和发病率一直在下降,这主要归功于早期筛查,但在发展中国家(包括中国)CRC的发病率处于增长趋势。在中国CRC的发病率在过去数十年里每年上升近4%1,2。值得注意的是,CRC患者的生存几率主要取决于诊断时肿瘤处于哪个阶段,在美国,所有CRC患者中只有40%的患者是在病灶处于原位时诊断出来的1,5。约有50%处于晚期的患者在得出最初诊断后五年内死亡,大多数死亡原因都是由于肿瘤转移,尤其是肝转移。因此,早期诊断和对已经转移的肿瘤新颖有效的治疗对于改善CRC患者的健康状况非常关键。
本发明就是本着方便使用人员,让使用人员可方便操作的目的,应运而生。
发明内容
本发明是通过以下技术方案实现:
一种评估CRC复发风险的诊断分析/预后分析方法,包括FGF18纤维母细胞生长因子18,PGR孕酮受体, ERBB2 v-erb-b2成红细胞的白血病病毒性致癌基因同系物2,神经/恶性胶质瘤衍生的致癌基因同系物(禽鸟), MKI67增殖标记Ki-67, BCL2 B-细胞慢性淋巴细胞性白血病/淋巴瘤2, INHBA人类抑制素,beta A
作为本发明的进一步优化方案,所述使用了149种主要浸润性乳腺肿瘤完整的人类基因组基因表达谱。
作为本发明的进一步优化方案,所述通过评估七种概率性分类器(包括复合协变量、线性判别、1-近邻法、3-近邻法、最近图心、支持向量机以及贝叶斯复合协变量算法)改进乳腺癌风险分类模型。
与现有的技术相比,本发明的有益效果是:本发明精确地判定活组织检查或者手术切除的肿瘤组织是否的确是结肠直肠癌,以及哪些患者癌症复发的几率高,然后根据判定结果选择根据患者肿瘤基因构造量身定制最有效的方案进行化学疗法。
具体实施方式
为了使本发明的目的、技术方案及优点更加清楚明白,以下结合实施例,对本发明进行进一步详细说明。应当理解,此处所描述的具体实施例仅仅用以解释本发明,并不用于限定本发明。
一种评估CRC复发风险的诊断分析/预后分析方法,包括FGF18纤维母细胞生长因子18, PGR孕酮受体, ERBB2 v-erb-b2成红细胞的白血病病毒性致癌基因同系物2,神经/恶性胶质瘤衍生的致癌基因同系物(禽鸟), MKI67增殖标记Ki-67, BCL2 B-细胞慢性淋巴细胞性白血病/淋巴瘤2, INHBA人类抑制素,beta A
作为本发明的进一步优化方案,所述使用了149种主要浸润性乳腺肿瘤完整的人类基因组基因表达谱。
作为本发明的进一步优化方案,所述通过评估七种概率性分类器(包括复合协变量、线性判别、1-近邻法、3-近邻法、最近图心、支持向量机以及贝叶斯复合协变量算法)改进乳腺癌风险分类模型。
以上所述仅为本发明的较佳实施例而已,并不用以限制本发明,凡在本发明的精神和原则之内所作的任何修改、等同替换和改进等,均应包含在本发明的保护范围之内。
Claims (3)
1.一种评估CRC复发风险的诊断分析/预后分析方法,包括FGF18纤维母细胞生长因子18, PGR孕酮受体, ERBB2 v-erb-b2成红细胞的白血病病毒性致癌基因同系物2,神经/恶性胶质瘤衍生的致癌基因同系物(禽鸟), MKI67增殖标记Ki-67, BCL2 B-细胞慢性淋巴细胞性白血病/淋巴瘤2, INHBA人类抑制素,beta A。
2.根据权利要求1所述的一种评估CRC复发风险的诊断分析/预后分析方法,其特征在于:使用了149种主要浸润性乳腺肿瘤完整的人类基因组基因表达谱。
3.根据权利要求1所述的一种评估CRC复发风险的诊断分析/预后分析方法,其特征在于:通过评估七种概率性分类器(包括复合协变量、线性判别、1-近邻法、3-近邻法、最近图心、支持向量机以及贝叶斯复合协变量算法)改进乳腺癌风险分类模型。
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CA2631720A1 (en) * | 2005-12-09 | 2007-09-13 | The Board Of Trustees Of The University Of Arkansas | Antineoplasics activities of ellipticine and its derivatives |
US8163896B1 (en) * | 2002-11-14 | 2012-04-24 | Rosetta Genomics Ltd. | Bioinformatically detectable group of novel regulatory genes and uses thereof |
CN102858985A (zh) * | 2009-07-24 | 2013-01-02 | 西格马-奥尔德里奇有限责任公司 | 基因组编辑方法 |
CN102971001A (zh) * | 2009-08-14 | 2013-03-13 | 阿勒根公司 | 使用生长因子再靶向内肽酶治疗癌症的方法 |
CN103517921A (zh) * | 2010-12-21 | 2014-01-15 | Abbvie公司 | IL-1-α和-β双特异性双重可变结构域免疫球蛋白及其用途 |
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US8163896B1 (en) * | 2002-11-14 | 2012-04-24 | Rosetta Genomics Ltd. | Bioinformatically detectable group of novel regulatory genes and uses thereof |
CA2631720A1 (en) * | 2005-12-09 | 2007-09-13 | The Board Of Trustees Of The University Of Arkansas | Antineoplasics activities of ellipticine and its derivatives |
CN102858985A (zh) * | 2009-07-24 | 2013-01-02 | 西格马-奥尔德里奇有限责任公司 | 基因组编辑方法 |
CN102971001A (zh) * | 2009-08-14 | 2013-03-13 | 阿勒根公司 | 使用生长因子再靶向内肽酶治疗癌症的方法 |
CN103517921A (zh) * | 2010-12-21 | 2014-01-15 | Abbvie公司 | IL-1-α和-β双特异性双重可变结构域免疫球蛋白及其用途 |
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