Zhang Yu, Wen Yuxin, Fan Peiyang, Li Fangfang, Li Muye, Wang Zhiyuan, Wang Xiaofang, Mao Zichen, Li Yanxun, Yao Yuchen, Bian Li
Department of Pathology, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
School of Basic Medical Sciences, Kunming Medical University, Kunming, Yunnan, China.
Discov Oncol. 2025 Sep 30;16(1):1780. doi: 10.1007/s12672-025-03621-w.
Brain metastases (BM) in non-small cell lung cancer (NSCLC) are associated with a poor prognosis. Identifying relevant genomic alterations can facilitate the targeting of therapies. We conducted a systematic review and meta-analysis to assess the prevalence and incidence of these alterations in NSCLC patients.
PubMed, Embase and WOS were searched, from January 2000 to February 2024 using "lung", "met" and "incidence" as search phrases. We obtained data on the prevalence at diagnosis and the annual incidence of new BM in patients with EGFR, ALK, KRAS, and other genetic alterations. The pooled prevalence and incidence rates were calculated using a random effects model. This study is registered with PROSPERO (CRD42023491178).
A total of 120 articles were included in the analysis. Prevalence data were derived from 94 studies (17,458 patients), while incidence data were obtained from 95 studies (13,323 patients). The pooled prevalence of BM at diagnosis was found to be 28.8% (95% [CI]: 0.263-0.313). This prevalence was highest among patients who were ALK-positive (31.6%) or had EGFR-positive (29.4%). The incidence rates were observed to be 0.086 in the EGFR group (95% CI 0.045-0.131), 0.062 in the ALK group (95% CI 0.003-0.122), 0.057 in the KRAS group (95% CI 0.000-0.188), 0.064 in the ROS1 group (95% CI 0.000-0.162), and 0.055 in the RET group (95% CI 0.000-0.224).
Comprehensive meta-analyses indicate prevalence and incidence of BM are higher in patients with specific genomic alterations and advanced disease. Brain imaging and targeted therapies for brain penetrance are important.
非小细胞肺癌(NSCLC)脑转移(BM)与预后不良相关。识别相关的基因组改变有助于靶向治疗。我们进行了一项系统评价和荟萃分析,以评估NSCLC患者中这些改变的患病率和发病率。
检索了2000年1月至2024年2月期间的PubMed、Embase和WOS,使用“肺”“转移”和“发病率”作为检索词。我们获得了诊断时的患病率以及表皮生长因子受体(EGFR)、间变性淋巴瘤激酶(ALK)、 Kirsten大鼠肉瘤病毒癌基因(KRAS)和其他基因改变患者中新发BM的年发病率数据。使用随机效应模型计算合并患病率和发病率。本研究已在国际前瞻性系统评价注册库(PROSPERO)注册(注册号:CRD42023491178)。
共有120篇文章纳入分析。患病率数据来自94项研究(17458例患者),而发病率数据来自95项研究(13323例患者)。诊断时BM的合并患病率为28.8%(95%置信区间[CI]:0.263 - 0.313)。这种患病率在ALK阳性(31.6%)或EGFR阳性(29.4%)的患者中最高。观察到EGFR组的发病率为0.086(95% CI 0.045 - 0.131),ALK组为0.062(95% CI 0.003 - 0.122),KRAS组为0.057(95% CI 0.000 - 0.188),ROS1组为0.064(95% CI 0.000 - 0.162),RET组为0.055(95% CI 0.000 - 0.224)。
综合荟萃分析表明,特定基因组改变和晚期疾病患者的BM患病率和发病率更高。脑成像和具有脑穿透性的靶向治疗很重要。