Department of Molecular Oncology, Cancer Institute (WIA), Chennai, India.
BMC Cancer. 2009 Oct 15;9:365. doi: 10.1186/1471-2407-9-365.
Cervical cancer is the most common cancer among Indian women. The current recommendations are to treat the stage IIB, IIIA, IIIB and IVA with radical radiotherapy and weekly cisplatin based chemotherapy. However, Radiotherapy alone can help cure more than 60% of stage IIB and up to 40% of stage IIIB patients.
Archival RNA samples from 15 patients who had achieved complete remission and stayed disease free for more than 36 months (No Evidence of Disease or NED group) and 10 patients who had failed radical radiotherapy (Failed group) were included in the study. The RNA were amplified, labelled and hybridized to Stanford microarray chips and analyzed using BRB Array Tools software and Significance Analysis of Microarray (SAM) analysis. 20 genes were selected for further validation using Relative Quantitation (RQ) Taqman assay in a Taqman Low-Density Array (TLDA) format. The RQ value was calculated, using each of the NED sample once as a calibrator. A scoring system was developed based on the RQ value for the genes.
Using a seven gene based scoring system, it was possible to distinguish between the tumours which were likely to respond to the radiotherapy and those likely to fail. The mean score +/- 2 SE (standard error of mean) was used and at a cut-off score of greater than 5.60, the sensitivity, specificity, Positive predictive value (PPV) and Negative predictive value (NPV) were 0.64, 1.0, 1.0, 0.67, respectively, for the low risk group.
We have identified a 7 gene signature which could help identify patients with cervical cancer who can be treated with radiotherapy alone. However, this needs to be validated in a larger patient population.
宫颈癌是印度女性中最常见的癌症。目前的建议是对 IIB 期、IIIA 期、IIIB 期和 IVA 期采用根治性放疗和每周顺铂为基础的化疗。然而,单独放疗可以帮助治愈超过 60%的 IIB 期和多达 40%的 IIIB 期患者。
本研究纳入了 15 名完全缓解且无疾病超过 36 个月(无疾病证据或 NED 组)和 10 名根治性放疗失败的患者(失败组)的存档 RNA 样本。RNA 被扩增、标记并与斯坦福微阵列芯片杂交,然后使用 BRB 阵列工具软件和微阵列信号分析(SAM)分析进行分析。选择了 20 个基因进行进一步验证,使用 Taqman 低密度阵列(TLDA)格式的相对定量(RQ)Taqman 测定法。使用每个 NED 样本作为校准物计算 RQ 值。基于基因的 RQ 值开发了一种评分系统。
使用基于七个基因的评分系统,可以区分对放疗有反应的肿瘤和可能失败的肿瘤。使用均值 +/- 2 SE(均值的标准误差),在截断值大于 5.60 时,低风险组的敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV)分别为 0.64、1.0、1.0、0.67。
我们已经确定了一个 7 基因标志物,可以帮助识别可以单独接受放疗的宫颈癌患者。然而,这需要在更大的患者群体中进行验证。