Ferris Robert L, Xi Liqiang, Raja Siva, Hunt Jennifer L, Wang Jun, Gooding William E, Kelly Lori, Ching Jesus, Luketich James D, Godfrey Tony E
Department of Otolaryngology and Immunology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Cancer Res. 2005 Mar 15;65(6):2147-56. doi: 10.1158/0008-5472.CAN-04-3717.
Clinical staging of cervical lymph nodes from patients with squamous cell carcinoma of the head and neck (SCCHN) has only 50% accuracy compared with definitive pathologic assessment. Consequently, both clinically positive and clinically negative patients frequently undergo neck dissections that may not be necessary. To address this potential overtreatment, sentinel lymph node (SLN) biopsy is currently being evaluated to provide better staging of the neck. However, to fully realize the potential improvement in patient care afforded by the SLN procedure, a rapid and accurate SLN analysis is necessary. We used quantitative reverse transcription-PCR (QRT-PCR) to screen 40 potential markers for their ability to detect SCCHN metastases to cervical lymph nodes. Seven markers were identified with good characteristics for identifying metastatic disease, and these were validated using a set of 26 primary tumors, 19 histologically positive lymph nodes, and 21 benign nodes from patients without cancer. Four markers discriminated between positive and benign nodes with accuracy >97% but only one marker, pemphigus vulgaris antigen (PVA), discriminated with 100% accuracy in both the observed data and a statistical bootstrap analysis. A rapid QRT-PCR assay for PVA was then developed and incorporated into a prototype instrument capable of performing fully automated RNA isolation and QRT-PCR. The automated analysis with PVA provided perfect discrimination between histologically positive and benign lymph nodes and correctly identified two lymph nodes with micrometastatic tumor deposits. These assays were completed (from tissue to result) in approximately 30 minutes, thus demonstrating the feasibility of intraoperative staging of SCCHN SLNs by QRT-PCR.
与最终病理评估相比,头颈部鳞状细胞癌(SCCHN)患者颈部淋巴结的临床分期准确性仅为50%。因此,临床阳性和临床阴性患者都经常接受可能不必要的颈部清扫术。为了解决这种潜在的过度治疗问题,目前正在对头颈部前哨淋巴结(SLN)活检进行评估,以提供更好的颈部分期。然而,要充分实现SLN手术为患者护理带来的潜在改善,快速准确的SLN分析是必要的。我们使用定量逆转录PCR(QRT-PCR)筛选了40种潜在标志物,以检测其检测SCCHN转移至颈部淋巴结的能力。确定了7种具有良好转移性疾病识别特征的标志物,并使用一组26例原发性肿瘤、19例组织学阳性淋巴结和21例来自无癌患者的良性淋巴结进行了验证。4种标志物区分阳性和良性淋巴结的准确率>97%,但只有一种标志物,即寻常型天疱疮抗原(PVA),在观察数据和统计自举分析中区分准确率均为100%。然后开发了一种针对PVA的快速QRT-PCR检测方法,并将其整合到一台能够进行全自动RNA分离和QRT-PCR的原型仪器中。使用PVA进行的自动分析能够完美区分组织学阳性和良性淋巴结,并正确识别出两个有微转移肿瘤沉积物的淋巴结。这些检测(从组织到结果)大约在30分钟内完成,从而证明了通过QRT-PCR对头颈部鳞状细胞癌前哨淋巴结进行术中分期的可行性。
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