Suppr超能文献

[靶向药物相关分子生物标志物表达在卵巢透明细胞癌中的临床意义]

[Clinical significance of targeting drug-based molecular biomarkers expression in ovarian clear cell carcinoma].

作者信息

Li M J, Li H R, Cheng X, Bi R, Tu X Y, Liu F, Chen L H

机构信息

Department of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2017 Dec 25;52(12):835-843. doi: 10.3760/cma.j.issn.0529-567x.2017.12.008.

Abstract

To assess the expression level of targeting drug-based molecular biomarkers in ovarian clear cell carcinoma (OCCC) tissues and its clinical significance. A total of 63 OCCC patients included 40 primary OCCC and 23 recurrent OCCC for secondary cytoreductive surgery (SCS), who had received primary surgeries at Fudan University Shanghai Cancer Center between January, 2008 and December, 2015 were enrolled, and immunohistochemistry SP method was used to test human epidermal growth factor receptor (EGFR), human epidermal growth factor receptor-2 (HER2), aurora kinase A (AURKA), breast cancer susceptibility gene 1 (BRCA1), BRCA2 and programmed death-ligand 1 (PD-L1)protein expression in paraffin-embedded tissues. The positive rates of EGFR, HER2, AURKA,BRCA1, BRCA2 and PD-L1 in primary and recurrent tumor tissues were respectively 20% (8/40) vs 30% (7/23) , 22% (9/40) vs 35% (8/23) , 38% (15/40) vs 35% (8/23) , 42% (17/40) vs 39% (9/23) , 20% (8/40) vs 22% (5/23) , 25% (10/40) vs 17% (4/23) , and there were no significant differences between primary and recurrent OCCC (all 0.05). χ(2)-test or Fisher exact analysis revealed that HER2 expression in recurrent tumor tissues had a relationship with chemoresistance (0.05), while the expression of other biomarkers showed no significant relationship with chemoresistance (all 0.05). Further, Kaplan-Meier survival analysis showed that patients with HER2 and AURKA-positive expression had a significantly shorter progression-free survival time in primary OCCC (4 months vs 10 months, log-rank test, 0.05 for HER2; and 4 months vs 10 months, 0.05 for AURKA); and a shorter overall survival time after SCS in recurrent OCCC (10 months vs 44 months, 0.05 for HER2; and 13 months vs 43 months, 0.05 for AURKA). However, multivariate Cox proportional hazards regression analysis indicated that none of these 6 biomarkers was independent risk factor of progression-free survival time of primary OCCC or overall survival time after SCS for recurrent OCCC (0.05). HER2 and AURKA could serve as prognostic factors in ovarian clear cell carcinoma.

摘要

评估靶向药物相关分子生物标志物在卵巢透明细胞癌(OCCC)组织中的表达水平及其临床意义。纳入2008年1月至2015年12月期间在复旦大学附属肿瘤医院接受初次手术的63例OCCC患者,其中包括40例原发性OCCC和23例接受二次肿瘤细胞减灭术(SCS)的复发性OCCC,采用免疫组织化学SP法检测石蜡包埋组织中人表皮生长因子受体(EGFR)、人表皮生长因子受体2(HER2)、极光激酶A(AURKA)、乳腺癌易感基因1(BRCA1)、BRCA2和程序性死亡配体1(PD-L1)蛋白的表达。原发性和复发性肿瘤组织中EGFR、HER2、AURKA、BRCA1、BRCA2和PD-L1的阳性率分别为20%(8/40)对30%(7/23)、22%(9/40)对35%(8/23)、38%(15/40)对35%(8/23)、42%(17/40)对39%(9/23)、20%(8/40)对22%(5/23)、25%(10/40)对17%(4/23),原发性和复发性OCCC之间差异均无统计学意义(均P>0.05)。χ²检验或Fisher确切概率法分析显示,复发性肿瘤组织中HER2表达与化疗耐药有关(P=0.05),而其他生物标志物的表达与化疗耐药无明显关系(均P>0.05)。此外,Kaplan-Meier生存分析显示,原发性OCCC中HER2和AURKA阳性表达的患者无进展生存期显著缩短(HER2:4个月对10个月,对数秩检验,P=0.05;AURKA:4个月对10个月,P=0.05);复发性OCCC中SCS后总生存期缩短(HER2:10个月对44个月,P=0.05;AURKA:13个月对43个月,P=0.05)。然而,多因素Cox比例风险回归分析表明,这6种生物标志物均不是原发性OCCC无进展生存期或复发性OCCC SCS后总生存期的独立危险因素(均P>0.05)。HER2和AURKA可作为卵巢透明细胞癌的预后因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验