Brennan J A, Mao L, Hruban R H, Boyle J O, Eby Y J, Koch W M, Goodman S N, Sidransky D
Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2195.
N Engl J Med. 1995 Feb 16;332(7):429-35. doi: 10.1056/NEJM199502163320704.
Surgical oncologists rely heavily on the histopathological assessment of surgical margins to ensure total excision of the tumor in patients with head and neck cancer. However, current techniques may not detect small numbers of cancer cells at the margins of resection or in cervical lymph nodes.
We used molecular techniques to determine whether clonal populations of infiltrating tumor cells harboring mutations of the p53 gene could be detected in histopathologically negative surgical margins and cervical lymph nodes of patients with squamous-cell carcinoma of the head and neck.
We identified 25 patients with primary squamous-cell carcinoma of the head and neck containing a p53 mutation who appeared to have had complete tumor resection on the basis of a negative histopathological assessment. In 13 of these 25 patients, molecular analysis was positive for a p53 mutation in at least one tumor margin. In 5 of 13 patients with positive margins by this method (38 percent), the carcinoma has recurred locally, as compared with none of 12 patients with negative margins (P = 0.02 by the log-rank test). Furthermore, molecular analysis identified neoplastic cells in 6 of 28 lymph nodes (21 percent) that were initially negative by histopathological assessment.
Among specimens initially believed to be negative by light microscopy, a substantial percentage of the surgical margins and lymph nodes from patients with squamous-cell carcinoma of the head and neck contained p53 mutations specific for the primary tumor. Patients with these positive margins appear to have a substantially increased risk of local recurrence. Molecular analysis of surgical margins and lymph nodes can augment standard histopathological assessment and may improve the prediction of local tumor recurrence.
外科肿瘤学家在很大程度上依赖手术切缘的组织病理学评估,以确保头颈癌患者的肿瘤被完全切除。然而,目前的技术可能无法检测到切除边缘或颈部淋巴结中的少量癌细胞。
我们使用分子技术来确定在头颈鳞状细胞癌患者的组织病理学阴性手术切缘和颈部淋巴结中,是否能检测到携带p53基因突变的浸润性肿瘤细胞的克隆群体。
我们确定了25例患有p53突变的原发性头颈鳞状细胞癌患者,基于组织病理学阴性评估,这些患者似乎已实现肿瘤完全切除。在这25例患者中的13例中,分子分析显示至少一个肿瘤切缘的p53突变呈阳性。通过这种方法切缘呈阳性的13例患者中有5例(38%)出现了局部复发,相比之下,12例切缘阴性的患者均未复发(对数秩检验P=0.02)。此外,分子分析在28个淋巴结中的6个(21%)中检测到肿瘤细胞,这些淋巴结最初组织病理学评估为阴性。
在最初通过光学显微镜检查被认为阴性的标本中,相当比例的头颈鳞状细胞癌患者的手术切缘和淋巴结含有原发性肿瘤特有的p53突变。这些切缘呈阳性的患者局部复发风险似乎大幅增加。手术切缘和淋巴结的分子分析可以加强标准的组织病理学评估,并可能改善对局部肿瘤复发的预测。