Division of Pulmonology and Critical Care Medicine, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Division of Pulmonary Medicine and Allergy, Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Republic of Korea.
Lung Cancer. 2019 Mar;129:28-34. doi: 10.1016/j.lungcan.2018.12.027. Epub 2018 Dec 28.
Patients with lung adenocarcinoma (ADC) are at higher risk of the development of brain metastasis (BM), and genetic alterations are associated with BM.
A total of 598 patients with lung ADC in our institution between January 2014 and December 2014 were reviewed retrospectively. We evaluated the incidence of BM by stage and genetic alterations.
Of the 598 patients, 97 (16.2%) had BM, which occurred across all stages. The incidence of BM showed a tendency to increase as the stage increased (p < 0.001, trend test). Although patients with EGFR mutations had BM across all stages, those with ALK or K- mutations had BM only in stage III and IV diseases. Regardless of types of mutations, the incidence of BM showed a tendency to increase as the T or N staging increased (p < 0.001 for each of EGFR, ALK, and K-RAS mutations, trend test). Whereas BM incidence showed a tendency to increase as the M staging increased in patients with EGFR-mutant lung ADC (p < 0.001, trend test), there was no linear trend between M staging and ALK (p = 0.469, trend test) or K-RAS mutations (p = 0.066, trend test). After adjusting covariables, EGFR mutations were associated with BM in never-smokers (adjusted OR = 2.07, 95% CI = 1.02-4.34) and K-RAS mutations were risk factors for BM in males (adjusted OR = 3.86, 95% CI = 1.01-14.43).
BM occurred in approximately 16% of lung ADC patients, including 3% with stage I diseases. Whereas EGFR-mutant lung ADC had BM across all stages, ALK- or K-RAS-mutant lung ADC had BM only in advanced stages. EGFR mutations were risk factors for BM among never-smokers and K-RAS mutations were risk factors among males.
肺腺癌(ADC)患者发生脑转移(BM)的风险较高,且遗传改变与 BM 相关。
回顾性分析了 2014 年 1 月至 2014 年 12 月我院收治的 598 例肺 ADC 患者。我们根据分期和遗传改变评估 BM 的发生率。
598 例患者中,97 例(16.2%)发生 BM,且发生于各分期。随着分期的增加,BM 的发生率呈上升趋势(p<0.001,趋势检验)。尽管 EGFR 突变患者各分期均有 BM,但 ALK 或 K-RAS 突变患者仅在 III 期和 IV 期疾病中有 BM。无论突变类型如何,随着 T 或 N 分期的增加,BM 的发生率呈上升趋势(EGFR、ALK 和 K-RAS 突变的趋势检验 p<0.001)。而在 EGFR 突变型肺 ADC 患者中,随着 M 分期的增加,BM 的发生率呈上升趋势(p<0.001,趋势检验),但 ALK(p=0.469,趋势检验)或 K-RAS 突变(p=0.066,趋势检验)与 M 分期之间无线性关系。调整协变量后,在从不吸烟者中,EGFR 突变与 BM 相关(调整 OR=2.07,95%CI=1.02-4.34),在男性中,K-RAS 突变是 BM 的危险因素(调整 OR=3.86,95%CI=1.01-14.43)。
BM 发生于约 16%的肺 ADC 患者中,包括 3%的 I 期疾病患者。EGFR 突变型肺 ADC 各分期均有 BM,而 ALK 或 K-RAS 突变型肺 ADC 仅在晚期发生 BM。EGFR 突变是从不吸烟者发生 BM 的危险因素,K-RAS 突变是男性发生 BM 的危险因素。