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在组织学阴性淋巴结中检测到K12-ras突变作为II期结直肠癌预后不良的指标。

Detection of mutated K12-ras in histologically negative lymph nodes as an indicator of poor prognosis in stage II colorectal cancer.

作者信息

Belly R T, Rosenblatt J D, Steinmann M, Toner J, Sun J, Shehadi J, Peacock J L, Raubertas R F, Jani N, Ryan C K

机构信息

Ortho-Clinical Diagnostics, Molecular Diagnostics Unit, 100 Indigo Creek Drive, Rochester, NY 14626, USA.

出版信息

Clin Colorectal Cancer. 2001 Aug;1(2):110-6. doi: 10.3816/CCC.2001.n.011.

DOI:10.3816/CCC.2001.n.011
PMID:12445369
Abstract

Stage II colorectal carcinoma is characterized by negative lymph node pathology as determined by conventional microscopic examination. These patients generally do not receive adjuvant therapy although 20%-30% will die from metastatic disease. To determine whether K-ras mutations at codon 12 could be used as a sensitive indicator of occult lymph node metastasis in stage II colon carcinoma, a retrospective study was performed using restriction endonuclease-mediated selective polymerase chain reaction (REMS-PCR) amplification. Of 106 colonic tumors analyzed, 46 were identified as positive for a K12-ras mutation in the primary tumor. Multiple lymph node samples from 38 of these 46 patients were examined by a sensitive nested PCR protocol for the presence of a K12-ras mutation. Of these 38 patients, 14 had 1 or more positive lymph nodes by PCR (37%) and 24 were negative for the mutation (63%). Of the 14 patients with a K12-ras mutation detected in lymph nodes, 8 died of the disease within 5 years (57%) compared to only 4 of the 24 patients with ras-negative lymph nodes (17%). The difference in time to death from disease, stratified using K12-ras status of lymph nodes, was statistically significant (P = 0.036; log-rank test). These results suggest K-ras mutation status of lymph nodes in patients with stage II colon cancer might identify a subgroup of patients who are more likely to develop recurrent and/or metastatic disease and benefit from adjuvant therapy. Larger studies are indicated to determine whether detection of K-ras mutation positivity in histologically negative lymph nodes portends a poor prognosis and to determine whether more aggressive use of adjuvant therapy is warranted.

摘要

II期结直肠癌的特征是通过传统显微镜检查确定淋巴结病理为阴性。这些患者通常不接受辅助治疗,尽管20%-30%会死于转移性疾病。为了确定密码子12处的K-ras突变是否可作为II期结肠癌隐匿性淋巴结转移的敏感指标,采用限制性内切酶介导的选择性聚合酶链反应(REMS-PCR)扩增进行了一项回顾性研究。在分析的106例结肠肿瘤中,46例被确定为原发肿瘤K12-ras突变阳性。对这46例患者中38例的多个淋巴结样本采用敏感的巢式PCR方案检测K12-ras突变的存在。在这38例患者中,14例通过PCR检测有1个或更多阳性淋巴结(37%),24例突变阴性(63%)。在淋巴结中检测到K-ras突变的14例患者中,8例在5年内死于该疾病(57%),而在24例ras阴性淋巴结患者中只有4例(17%)。根据淋巴结的K12-ras状态分层,疾病死亡时间的差异具有统计学意义(P = 0.036;对数秩检验)。这些结果表明,II期结肠癌患者淋巴结的K-ras突变状态可能识别出更易发生复发和/或转移性疾病并可能从辅助治疗中获益的患者亚组。需要进行更大规模的研究来确定在组织学阴性的淋巴结中检测到K-ras突变阳性是否预示预后不良,以及是否有必要更积极地使用辅助治疗。

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