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p53和ki67表达作为T1期移行细胞膀胱癌癌症相关生存的预后因素

p53 and ki67 expression as prognostic factors for cancer-related survival in stage T1 transitional cell bladder carcinoma.

作者信息

Rodríguez-Alonso Andrés, Pita-Fernández Salvador, González-Carreró Joaquín, Nogueira-March José Luis

机构信息

Urology Service, Xeral-Cíes Hospital, Vigo, Spain.

出版信息

Eur Urol. 2002 Feb;41(2):182-8; discussion 188-9. doi: 10.1016/s0302-2838(01)00038-0.


DOI:10.1016/s0302-2838(01)00038-0
PMID:12074407
Abstract

OBJECTIVE: To determine prognostic factors for survival in bladder transitional cell carcinoma (TCC), and the prognostic value of p53 and ki67. MATERIAL AND METHODS: A study was made of patients with stage T1 primary bladder TCC (n = 175). The immunohistochemical study was carried out using DO7 and MIB-1 monoclonal antibodies, for p53 and ki67, respectively. Kaplan-Meier methodology was used for the survival analysis, and the log-rank test was applied in order to determine accumulated probability rates of survival. Moreover, Cox's multivariate regression analysis was also used to establish the variables associated with survival. Receiver operating characteristic (ROC) curves were also drawn, with the aim of determining the prognostic capacity of p53 and ki67. RESULTS: The average follow-up period was 7.3 years. Cancer-related survival rates at 5 and 10 years were 89.51 and 80.68%, respectively. The increase in p53 and ki67 expressions paralleled the histological grade, both markers showing significant inter-group differences (P = 0.0000). The variables which modified cancer-related survival significantly in the univariate analysis were the following: tumour multifocality, solid microscopic morphology, large cell nucleus and a high expression of p53 and ki67. Independent cancer-related survival variables were: age, tumour size of >3 cm, a solid microscopic growth pattern and expression of p53. CONCLUSIONS: The expression of p53, increase in age, tumour size of >3 cm and microscopic growth pattern are independent predictors for cancer-related survival. A positive correlation was observed, indicating that, the higher the expression of p53, the greater the probability of death.

摘要

目的:确定膀胱移行细胞癌(TCC)生存的预后因素,以及p53和ki67的预后价值。 材料与方法:对175例T1期原发性膀胱TCC患者进行了研究。分别使用DO7和MIB-1单克隆抗体对p53和ki67进行免疫组化研究。采用Kaplan-Meier方法进行生存分析,并应用对数秩检验来确定累积生存率。此外,还使用Cox多因素回归分析来确定与生存相关的变量。绘制受试者工作特征(ROC)曲线,以确定p53和ki67的预后能力。 结果:平均随访期为7.3年。5年和10年的癌症相关生存率分别为89.51%和80.68%。p53和ki67表达的增加与组织学分级平行,两种标志物在组间均显示出显著差异(P = 0.0000)。单因素分析中显著改变癌症相关生存的变量如下:肿瘤多灶性、实体显微镜形态、大细胞核以及p53和ki67的高表达。独立的癌症相关生存变量为:年龄、肿瘤大小>3 cm、实体显微镜生长模式和p53表达。 结论:p53表达、年龄增加、肿瘤大小>3 cm和显微镜下生长模式是癌症相关生存的独立预测因素。观察到正相关,表明p53表达越高,死亡概率越大。

相似文献

[1]
p53 and ki67 expression as prognostic factors for cancer-related survival in stage T1 transitional cell bladder carcinoma.

Eur Urol. 2002-2

[2]
[Multivariate analysis of recurrence and progression in stage T1 transitional-cell carcinoma of the bladder. Prognostic value of p53 and Ki67].

Actas Urol Esp. 2003-2

[3]
Evaluation of P53 protein overexpression, Ki67 proliferative activity and mitotic index as markers of tumour recurrence in superficial transitional cell carcinoma of the bladder.

Eur Urol. 2000-9

[4]
Multivariate analysis of survival, recurrence, progression and development of mestastasis in T1 and T2a transitional cell bladder carcinoma.

Cancer. 2002-3-15

[5]
Prognostic value of MCM2 immunoreactivity in stage T1 transitional cell carcinoma of the bladder.

Eur Urol. 2003-2

[6]
Prognostic factors in stage T1 grade 3 bladder cancer survival: the role of G1-S modulators (p53, p21Waf1, p27kip1, Cyclin D1, and Cyclin D3) and proliferation index (ki67-MIB1).

Eur Urol. 2004-5

[7]
p53 expression predicts progression and poor survival in T1 bladder tumours.

Eur Urol. 2000-6

[8]
Prognostic value of the combined expression of tumor-associated trypsin inhibitor (TATI) and p53 in patients with bladder cancer undergoing radical cystectomy.

Cancer Biomark. 2019

[9]
Evaluation of overexpression of p53 tumor suppressor protein in superficial and invasive transitional cell bladder cancer: comparison with DNA ploidy.

Urology. 1995-9

[10]
Apoptosis, proliferation and p53, cyclin D1, and retinoblastoma gene expression in relation to radiation response in transitional cell carcinoma of the bladder.

Int J Radiat Oncol Biol Phys. 2001-4-1

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[3]
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[6]
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[7]
Prognostic value of ki67 in BCG-treated non-muscle invasive bladder cancer: a meta-analysis and systematic review.

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[8]
Impact of the Ki-67 labeling index and p53 expression status on disease-free survival in pT1 urothelial carcinoma of the bladder.

Transl Androl Urol. 2017-12

[9]
ESR1, ERBB2, and Ki67 mRNA expression predicts stage and grade of non-muscle-invasive bladder carcinoma (NMIBC).

Virchows Arch. 2016-11

[10]
Role of morphometry and proliferative parameters in grading of urothelial neoplasms.

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