Hayashi Masamichi, Wu Gaosong, Roh Jong-Lyel, Chang Xiaofei, Li Xiufeng, Ahn Julie, Goldsmith Marla, Khan Zubair, Bishop Justin, Zhang Zhe, Zhou Xian Chong, Richmon Jeremy, Agrawal Nishant, Koch Wayne M
Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Cancer. 2015 Jun 15;121(12):1957-65. doi: 10.1002/cncr.29303. Epub 2015 Mar 13.
Securing negative surgical margins is a critical goal for head and neck surgery. Local recurrence develops even in some patients who have histologically negative surgical margins. Minimal residual tumor cells may lead to locoregional recurrence despite clear histologic margins reported at the time of resection of head and neck squamous cell carcinoma (HNSCC). To identify subclinical residual disease, the authors analyzed deep margin imprint samples collected on 1-layer nitrocellulose sheets.
Bisulfite-treated DNA samples from 73 eligible patients were amplified by quantitative methylation-specific polymerase chain reaction (QMSP) targeting 6 genes (deleted in colorectal cancer [DCC], endothelin receptor type B [EDNRB], homeobox protein A9 [HOXA9], kinesin family member 1A [KIF1A], nidogen-2 [NID2], and N-methyl D-aspartate receptor subtype 2B [NR2B]). QMSP values were dichotomized as positive or negative. Associations between the QMSP status of deep margin samples and clinical outcomes were evaluated.
Two-gene methylation combinations among the genes DCC, EDNRB, and HOXA9 were associated with decreased locoregional recurrence-free survival, recurrence-free survival, and overall survival. The methylated gene combination of EDNRB and HOXA9 in margin imprints was the most powerful predictor of poor locoregional recurrence-free survival (hazard ratio [HR], 3.31; 95% confidence interval [CI], 1.30-8.46; P = .012) independent of standard histologic factors. In addition, methylation of both EDNRB and HOXA9 indicated a trend toward reduced recurrence-free survival (HR, 2.74; 95% CI, 0.90-8.33; P = .075) and reduced OS (HR, 5.78; 95% CI, 0.75-44.7; P = .093) in multivariable analysis.
A panel of gene methylation targets in deep surgical margin imprints provides a potential predictive marker of postoperative locoregional recurrence. Intraoperative use of molecular margin imprint analysis may assist surgeons in obtaining rigorously negative surgical margins and improve the outcome of head and neck surgery.
确保手术切缘阴性是头颈外科手术的关键目标。即使在一些手术切缘组织学检查为阴性的患者中也会发生局部复发。尽管在头颈部鳞状细胞癌(HNSCC)切除时报告切缘组织学检查清晰,但微小残留肿瘤细胞仍可能导致局部区域复发。为了识别亚临床残留疾病,作者分析了在单层硝酸纤维素膜上收集的深部切缘印记样本。
对73例符合条件的患者经亚硫酸氢盐处理的DNA样本,采用定量甲基化特异性聚合酶链反应(QMSP)扩增靶向6个基因(结直肠癌缺失基因[DCC]、内皮素B型受体[EDNRB]、同源盒蛋白A9[HOXA9]、驱动蛋白家族成员1A[KIF1A]、巢蛋白-2[NID2]和N-甲基-D-天冬氨酸受体2B亚型[NR2B])。QMSP值分为阳性或阴性。评估深部切缘样本的QMSP状态与临床结局之间的关联。
DCC、EDNRB和HOXA9基因中的双基因甲基化组合与局部区域无复发生存率、无复发生存率和总生存率降低相关。切缘印记中EDNRB和HOXA9的甲基化基因组合是局部区域无复发生存率差的最有力预测指标(风险比[HR],3.31;95%置信区间[CI],1.30 - 8.46;P = 0.012),独立于标准组织学因素。此外,在多变量分析中,EDNRB和HOXA9均甲基化表明无复发生存率降低(HR,2.74;95% CI,0.90 - 8.33;P = 0.075)和总生存率降低(HR,5.78;95% CI,0.75 - 44.7;P = 0.093)的趋势。
深部手术切缘印记中的一组基因甲基化靶点可提供术后局部区域复发的潜在预测标志物。术中使用分子切缘印记分析可能有助于外科医生获得严格的阴性手术切缘并改善头颈外科手术的结局。