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基于真实世界肺腺癌脑转移患者的预后因素分析

Prognostic Factors of Real-World Lung Adenocarcinoma Patients with Brain Metastases

  • 摘要:
    目的 通过对129例肺腺癌(LUAD)脑转移患者的临床资料进行回顾性分析,寻找其预后不良相关指标。
    方法 回顾性分析了2018年5月—2023年5月就诊于兰州大学第一医院、符合入组标准的129例LUAD脑转移患者的临床资料,通过查阅患者电子病历、电话咨询等方式进行随访,随防至2024年5月。单因素生存分析采用Kaplan-Meier法并绘制生存曲线,将有意义的结果纳入多因素Cox回归模型,进一步明确影响LUAD脑转移患者生存的不良预后因素。
    结果 病理学形态、KPS评分、脑转移数目、有无基因变异、基因变异的个数和形式、是否为EGFR变异、Cyfra-211、NLR水平等因素均与患者的生存预后显著相关(P<0.05)。Cox回归多因素结果表明病理学形态、KPS评分、脑转移数目、初诊时NLR比值、有无基因变异等因素是LUAD脑转移患者预后的独立影响因素(P<0.05)。对不同治疗亚组的生存情况进行分析,发现联合治疗可明显提高患者的中位生存期,差异有统计学意义(P=0.034)。
    结论 实体型和复杂腺体结构、KPS<80分、脑转移数目≥3、初诊时NLR水平升高、有基因变异是LUAD脑转移患者的独立预后不良因素;联合治疗可明显延长患者的生存期。

     

    Abstract:
    Objective To identify the indicators associated with poor prognosis by retrospectively analyzing the clinical data of 129 patients with lung adenocarcinoma (LUAD) complicated by brain metastases (BMs).
    Methods We retrospectively assessed the clinical data of 129 LUAD patients with BMs who met the inclusion criteria. Follow-up was conducted through electronic medical record review and telephone consultations. Univariate survival analysis was performed using the Kaplan-Meier method with corresponding survival curves. Statistically significant variables identified in the univariate analysis were subsequently incorporated into a multivariate Cox proportional hazards regression model to further identify independent adverse prognostic factors affecting the survival of LUAD patients with BMs.
    Results The following factors were significantly associated with patient survival prognosis (P<0.05): pathological morphology, KPS score, number of BMs, presence of genetic variations, quantity of genetic variations, type of genetic variations, EGFR mutation status, Cyfra-211, and neutrophil-to-lymphocyte ratio (NLR) at initial diagnosis. Multivariate Cox regression analysis revealed that pathological morphology, KPS score, number of BMs, NLR at initial diagnosis, and presence of genetic variations served as independent prognostic factors for LUAD patients with BMs (P<0.05). Further analysis of the survival conditions of different treatment subgroups revealed that combined therapy could significantly increase the median survival period of patients, and the difference was statistically significant (P=0.034).
    Conclusion Solid and complex glandular structures, KPS score <80, ≥3 BMs, elevated NLR levels at initial diagnosis, and the presence of genetic alterations are identified as independent poor prognostic factors for LUAD patients with BMs. Combination therapy can significantly prolong the survival of patients.

     

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