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基于人群资料构建肾肉瘤样癌Nomogram预后模型
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作者 李浩 贾占奎 +1 位作者 李健 彭浩 《现代泌尿外科杂志》 CAS 2020年第11期998-1002,1042,共6页
目的基于人群资料构建肾肉瘤样癌预后预测模型,进行个体化预后评估。方法筛选2004至2016年美国Surveillance、Epidemiology及End Results数据库中的984例肾肉瘤样癌患者作为研究对象,采用单因素和多因素Fine and Gray和Cox比例风险回归... 目的基于人群资料构建肾肉瘤样癌预后预测模型,进行个体化预后评估。方法筛选2004至2016年美国Surveillance、Epidemiology及End Results数据库中的984例肾肉瘤样癌患者作为研究对象,采用单因素和多因素Fine and Gray和Cox比例风险回归模型确定肾肉瘤样癌的独立预后风险因素,并用Nomogram构建预测模型,同时运用Calibration检测预测一致性。结果所有患者进行了根治性肾切除术,中位总生存期为11个月,多因素竞争风险模型回归分析提示肿瘤直径(HR=1.03,95%CI:1.01~1.06,P<0.001)、肿瘤T分期(T3相对T1;HR=1.56,95%CI:1.17~2.08,P<0.001)、N分期(HR=1.70,95%CI:1.43~2.04,P<0.001)、M分期(HR=2.09,95%CI:1.78~2.46,P<0.001)是肉瘤样癌预后的独立预测因素。根据其结果建立Nomogram模型,该模型预测能力较好(C-index=0.763)。结论成功构建肉瘤样癌肿瘤特异性死亡风险预后预测模型,为该类疾病提供个体化预后预测信息,有一定临床实际应用价值;同时该研究存在一定的局限性,需要外部数据进行验证。 展开更多
关键词 肾肉瘤样癌 SEER数据库 NOMOGRAM 预测模型 人群资料
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儿童与成人单纯性睾丸卵黄囊瘤临床特点对比分析 被引量:1
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作者 于顺利 罗彬杰 +5 位作者 翟天元 周乃春 金志波 贾占奎 杨锦建 顾朝辉 《中华男科学杂志》 CAS CSCD 北大核心 2019年第2期144-149,共6页
目的:通过对比儿童与成人单纯睾丸卵黄囊瘤的特点,提高睾丸卵黄囊瘤的诊疗水平。方法:选取2008年5月至2018年7月病理确诊的单纯性睾丸卵黄囊瘤75例患者为研究对象,其中64例患者年龄<18岁设为儿童组,11例患者年龄≥18岁设为成人组。... 目的:通过对比儿童与成人单纯睾丸卵黄囊瘤的特点,提高睾丸卵黄囊瘤的诊疗水平。方法:选取2008年5月至2018年7月病理确诊的单纯性睾丸卵黄囊瘤75例患者为研究对象,其中64例患者年龄<18岁设为儿童组,11例患者年龄≥18岁设为成人组。回顾性分析所有患者的临床资料,比较两组患者临床表现、实验室检查、病理学表现、临床分期、治疗方案及预后。结果:儿童组年龄6个月至5岁[(1.38±0.89)岁],肿瘤大小0.9~6.0(2.48±1.12) cm;成人组年龄25~49岁,中位年龄34(29,46)岁,肿瘤大小3.5~6.3(5.16±1.32) cm;两组最常见的就诊原因为患侧睾丸无痛性肿大,4例(6.3%)儿童,5例(45.5%)成人以睾丸疼痛就诊。儿童与成人组肿瘤直径及首诊表现差异有统计学意义(P<0.05)。所有患者均行根治性高位精索离断式睾丸切除术,儿童组24例行化疗,1例行腹膜后淋巴结清扫术(RPLND);成人组5例行化疗,3例行RPLND。所有患者术前甲胎蛋白(AFP)均不同程度升高。病理结果示肿瘤细胞小,核仁明显,胞质多空泡,形态不规则,细胞排列疏松,细胞内外可见透明小体。10例患者失访,余65例随访10~78(52.00±23.78)个月;儿童组2例单纯转移,3例单纯复发,3例复发伴转移,5例死亡;成人组5例单纯转移,1例单纯复发,1例复发伴转移,4例死亡。结论:成人与儿童睾丸卵黄囊瘤在临床表现、生物学行为、治疗、预后等方面有很大区别。儿童睾丸卵黄囊瘤患者多为临床I期,首选根治性睾丸切除术,预后良好;成人患者恶性程度较高,易复发和转移,预后较差,应联合根治性睾丸切除术、RPLND及化疗等治疗方式。 展开更多
关键词 睾丸肿瘤 卵黄囊瘤 内胚窦瘤 成人 儿童
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Apoptosis of non-tumor cells contributes to increased serum cytochrome c level in a neuroblastoma xenograft model 被引量:1
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作者 Zhang Da Yu Jie-kai +7 位作者 Yang Fu-quan Wang Lei Zhang Guo-feng Meng Qing-lei Mu Xin Ma Wei jia zhan-kui Wang jia-xiang 《Chinese Medical Journal》 SCIE CAS CSCD 2012年第2期316-320,共5页
Background Neuroblastoma (NB) is one of the most common malignant solid tumors of childhood.It is still not clear whether the apoptosis of tumor cells or the non-tumor cells contributes to the increase of concentrat... Background Neuroblastoma (NB) is one of the most common malignant solid tumors of childhood.It is still not clear whether the apoptosis of tumor cells or the non-tumor cells contributes to the increase of concentration of cytochrome c (Cyt c) in the serum of the cancer patients.The aim of this research was to identify the source of the Cyt c in the serum when the tumor grows up by subcutaneous inoculation of human NB cells into nude mice.Methods We subcutaneously inoculated human NB cells (KP-N-NS) into nude mice and collected the sera of tumor-bearing mice (n=14) and control mice (n=25) 4 weeks later in order to screen for and identify differentially expressed proteins in the serum.Differentially expressed proteins in the serum were screened by surface-enhanced laser desorption/ionization-time-of-fiight (SELDI-TOF) mass spectrometry.Results The relative intensity of a protein having a mass-to-charge ratio (m/z) of 11 609 was 3338.37±3410.85 in the tumor group and 59.84±40.74 in the control group,indicating that the expression level of this protein in the tumor group was 55.8 times higher than that in the control group.Serum proteins were separated and purified by high-performance liquid chromatography (HPLC).Liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) was performed to produce peptide mass fingerprints (PMFs).Spectrum analysis and a database search revealed that the highly expressed protein (m/z=11605.4) from the serum of tumor-bearing mice was the mouse Cyt c.Conclusions Increased concentration of Cyt c in the serum of tumor-bearing nude mice might be partially attributed to the secretion of this protein by non-tumor cells. 展开更多
关键词 NEUROBLASTOMA cytochrome c APOPTOSIS protein array analysis
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Discovery and identification of serum biomarkers of Wilms' tumor in mice using proteomics technology
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作者 jia zhan-kui WANG jia-xiang +5 位作者 YANG Jin-iian XUE Rui ZHANG Da WANG Guan-nan MA Sheng-li DUAN Zhen-feng 《Chinese Medical Journal》 SCIE CAS CSCD 2012年第10期1727-1732,共6页
Background Wilms' tumor (nephroblastoma) is a cancer of the kidneys that occurs typically in children and rarely in adults. Early diagnosis is very important for the treatment and prognosis of the disease. The aim ... Background Wilms' tumor (nephroblastoma) is a cancer of the kidneys that occurs typically in children and rarely in adults. Early diagnosis is very important for the treatment and prognosis of the disease. The aim of our study was to discover and identify potential non-invasive and convenient biomarkers for the diagnosis of Wilms' tumor. Methods Nude mice were used to construct a Wilms' tumor model by injecting nephroblastoma cells into their bilateral abdomen. We collected 94 serum samples from mice consisting of 45 samples with Wilms' tumor and 49 controls. The serum proteomic profiles of the samples were analyzed via surface-enhanced laser desorption/ionization time-of-flight mass spectrometry. The candidate biomarkers were purified by high-performance liquid chromatography, identified by liquid chromatography-mass spectrometry, and validated using ProteinChip immunoassays. Results We finally retrieved two differential proteins (mlz 4509.2; 6207.9), which were identified as apolipoprotein A-II and polyubiquitin, respectively. The expression of apolipoprotein A-II was higher in the Wilms' tumor group than in the control group (P 〈0.01). By contrast, the expression of polyubiquitin was lower in the Wilms' tumor group than in the control group. Conclusion Apolipoprotein A-II and polyubiquitin may be used as potential biomarkers for nephroblastoma in children, and the analysis of apolipoprotein A-II may help diagnose and treat Wilms' tumor. 展开更多
关键词 PROTEOMICS Wilms tumor biomarker
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