医学
克拉斯
危险系数
结直肠癌
内科学
肿瘤科
原发性肿瘤
比例危险模型
队列
胃肠病学
癌症
置信区间
转移
作者
Georgios Antonios Margonis,Neda Amini,Stefan Buettner,Yuhree Kim,Jane Wang,Nikolaos Andreatos,Doris Wagner,Kazunari Sasaki,Andrea Beer,Carsten Kamphues,Daisuke Morioka,Inger Marie Løes,Katsunori Imai,Jin He,Timothy M. Pawlik,Klaus Kaczirek,George A. Poultsides,Per Eystein Lønning,Richard A. Burkhart,Itaru Endo
出处
期刊:Annals of Surgery
[Lippincott Williams & Wilkins]
日期:2019-08-05
卷期号:273 (6): 1165-1172
被引量:38
标识
DOI:10.1097/sla.0000000000003504
摘要
OBJECTIVE: To examine the prognostic impact of tumor laterality in colon cancer liver metastases (CLM) after stratifying by Kirsten rat sarcoma 2 viral oncogene homolog (KRAS) mutational status. BACKGROUND: Although some studies have demonstrated that patients with CLM from a right sided (RS) primary cancer fare worse, others have found equivocal outcomes of patients with CLM with RS versus left-sided (LS) primary tumors. Importantly, recent evidence from unresectable metastatic CRC suggests that tumor laterality impacts prognosis only in those with wild-type tumors. METHODS: Patients with rectal or transverse colon tumors and those with unknown KRAS mutational status were excluded from analysis. The prognostic impact of RS versus LS primary CRC was determined after stratifying by KRAS mutational status. RESULTS: 277 patients had a RS (38.6%) and 441 (61.4%) had a LS tumor. Approximately one-third of tumors (28.1%) harbored KRAS mutations. In the entire cohort, RS was associated with worse 5-year overall survival (OS) compared with LS (39.4% vs 50.8%, P = 0.03) and remained significantly associated with worse OS in the multivariable analysis (hazard ratio 1.45, P = 0.04). In wild-type patients, a worse 5-year OS associated with a RS tumor was evident in univariable analysis (43.7% vs 55.5%, P = 0.02) and persisted in multivariable analysis (hazard ratio 1.49, P = 0.01). In contrast, among patients with KRAS mutated tumors, tumor laterality had no impact on 5-year OS, even in the univariable analysis (32.8% vs 34.0%, P = 0.38). CONCLUSIONS: This study demonstrated, for the first time, that the prognostic impact of primary tumor side differs according to KRAS mutational status. RS tumors were associated with worse survival only in patients with wild-type tumors.
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