Sharie Ahmed H Al, Jadallah Rami K, Al-Bataineh Mahmoud Z, Obeidat Lana E, Lataifeh Hanin, Tarad Mahmoud I, Khasawneh Mustafa Q, Almdallal Walaa, El-Elimat Tamam, Alali Feras Q
Department of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
King Abdullah University Hospital, Irbid, Jordan.
Cancer Control. 2025 Jan-Dec;32:10732748251325587. doi: 10.1177/10732748251325587. Epub 2025 Mar 24.
IntroductionLung adenocarcinoma is the leading cause of cancer-related mortality worldwide. Understanding the clinicopathological profiles and genomic drivers of its metastatic patterns is a crucial step for risk stratification. Herein, we investigated the clinicogenomic features of bone metastases in lung adenocarcinoma and their prognostic value.MethodsA retrospective cohort study with a total of 4064 patients with various metastatic patterns of lung adenocarcinoma were included, obtaining relevant clinical data and genomic profiles. Patients were categorized based on the presence or absence of bone metastases. A comparative analysis of both groups in terms of demographics, disease status, somatic mutations, and microsatellite instability was carried out. Significantly different variables were tested for their association with bone metastases. Cox regression analyses were utilized to identify independent survival prognostic variables in the bone metastases sub-cohort.ResultsGender, concomitant metastases (to adrenal gland, nervous system, lymph nodes, liver, lung, mediastinum, pleura, and skin), and aberrations in , , , and were associated with bone metastases in lung adenocarcinoma. Survival analyses within the bone metastases sub-cohort have illustrated the following variables to possess poor prognostic signature including age > 75, female gender, White ethnicity, distant metastases (adrenal gland, central nervous system, intra-abdominal, and liver), (wild type), (mutant), (mutant), (mutant), and (mutant).ConclusionKey clinical and genomic factors associated with lung adenocarcinoma bone metastases have been highlighted, providing exploratory insights into high-risk individuals. Future studies should be directed to validate these prognostic variables in larger, more diverse cohorts to enhance generalizability.
引言
肺腺癌是全球癌症相关死亡的主要原因。了解其转移模式的临床病理特征和基因组驱动因素是风险分层的关键步骤。在此,我们研究了肺腺癌骨转移的临床基因组特征及其预后价值。
方法
纳入一项回顾性队列研究,共纳入4064例具有各种转移模式的肺腺癌患者,获取相关临床数据和基因组图谱。根据是否存在骨转移对患者进行分类。对两组在人口统计学、疾病状态、体细胞突变和微卫星不稳定性方面进行比较分析。对显著不同的变量测试其与骨转移的相关性。利用Cox回归分析确定骨转移亚组中的独立生存预后变量。
结果
性别、伴随转移(至肾上腺、神经系统、淋巴结、肝脏、肺、纵隔、胸膜和皮肤)以及 、 、 和 的异常与肺腺癌骨转移相关。骨转移亚组内的生存分析表明,以下变量具有不良预后特征,包括年龄>75岁、女性、白种人、远处转移(肾上腺、中枢神经系统、腹腔内和肝脏)、 (野生型)、 (突变型)、 (突变型)、 (突变型)和 (突变型)。
结论
已突出显示了与肺腺癌骨转移相关的关键临床和基因组因素,为高危个体提供了探索性见解。未来的研究应致力于在更大、更多样化的队列中验证这些预后变量,以提高普遍性。