Hasanzadeh Malihe, Sharifi Nourieh, Esmaieli Habibollah, Daloee Mahdi Sharife, Tabari Azadeh
Department of Gynecology Oncology, Women's Health Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
J Obstet Gynaecol Res. 2013 Feb;39(2):572-7. doi: 10.1111/j.1447-0756.2012.01981.x. Epub 2012 Aug 26.
Considering that Ki-67 is a proliferative marker in molar pregnancies and the possible progression of these kinds of pregnancies to gestational trophoblastic neoplasia (GTN), we decided to evaluate the rate of expression of this marker in patients with uneventful hydatidiform moles and GTN. Moreover, we determined the predictive value of this factor for the progression of molar pregnancies to GTN.
In two groups of patients, including 30 patients with uneventful molar pregnancies and 30 patients with GTN, an immunohistochemical staining technique using the Envision method was performed. To evaluate nuclear immunoreactivity of trophoblastic cells for Ki67 on paraffin sections obtained from molar pregnancy products, the percentage of the stained cells was used. Semi-quantitative evaluation was also performed. Data were analyzed using Mann-Whitney tests and receiver operating characteristic curve analysis.
The expression of Ki67 in cytotrophoblastic and syncytiotrophoblastic cells of patients with GTN was significantly more than for patients with an uneventful molar pregnancy (P<0.05). We considered a 12.5% cut-off value for Ki67 in cytotrophoblastic cells and a sensitivity of 90%, specificity 93%, positive predictive value of 93.1% and negative predictive value of 90.3% were obtained. Similarly, considering a cut-off value of 6% for Ki67 in syncytiotrophoblastic cells, results of 90% were obtained for all diagnostic indices.
Our findings suggest that expression of the Ki67 oncogene in trophoblastic cells in patients with GTN are found far more frequently than in patients with an uneventful molar pregnancy, and demonstrate a high predictive value of progression to GTN.
鉴于Ki-67是葡萄胎妊娠中的增殖标志物,且这类妊娠可能进展为妊娠滋养细胞肿瘤(GTN),我们决定评估该标志物在葡萄胎妊娠结局良好患者及GTN患者中的表达率。此外,我们还确定了该因素对葡萄胎妊娠进展为GTN的预测价值。
对两组患者进行研究,其中一组为30例葡萄胎妊娠结局良好的患者,另一组为30例GTN患者,采用Envision法进行免疫组织化学染色技术检测。为评估从葡萄胎妊娠产物石蜡切片中滋养层细胞对Ki67的核免疫反应性,采用染色细胞百分比进行评估。同时进行半定量评估。数据采用Mann-Whitney检验和受试者工作特征曲线分析。
GTN患者的细胞滋养层细胞和合体滋养层细胞中Ki67的表达显著高于葡萄胎妊娠结局良好的患者(P<0.05)。我们将细胞滋养层细胞中Ki67的临界值设定为12.5%,其敏感性为90%,特异性为93%,阳性预测值为93.1%,阴性预测值为90.3%。同样,将合体滋养层细胞中Ki67的临界值设定为6%时,所有诊断指标的结果均为90%。
我们的研究结果表明,GTN患者滋养层细胞中Ki67癌基因的表达远比葡萄胎妊娠结局良好的患者更为常见,且显示出对进展为GTN具有较高的预测价值。