Nie Weihao, Jiang Yiheng, Yao Luhan, Zhu Xinqing, Al-Danakh Abdullah Y, Liu Wenlong, Chen Qiwei, Yang Deyong
Department of Urology, First Affiliated Hospital of Dalian Medical University, Dalian, 116021, China.
School of Information and Communication Engineering, Dalian University of Technology, Dalian, China.
Heliyon. 2024 Oct 23;10(23):e39327. doi: 10.1016/j.heliyon.2024.e39327. eCollection 2024 Dec 15.
Bladder cancer (BCa) is a heterogeneous malignancy characterized by distinct immune subtypes, primarily due to differences in tumor-infiltrating immune cells and their functional characteristics. Therefore, understanding the tumor immune microenvironment (TIME) landscape in BCa is crucial for prognostic prediction and guiding precision therapy. In this study, we integrated 10 machine learning algorithms to develop an immune-related machine learning signature (IRMLS) and subsequently created a deep learning model to detect the IRMLS subtype based on pathological images. The IRMLS proved to be an independent prognostic factor for overall survival (OS) and demonstrated robust and stable performance (p < 0.01). The high-risk group exhibited an immune-inflamed phenotype, associated with poorer prognosis and higher levels of immune cell infiltration. We further investigated the cancer immune cycle and mutation landscape within the IRMLS model, confirming that the high-risk group is more sensitive to immune checkpoint immunotherapy (ICI) and adjuvant chemotherapy with cisplatin (p = 2.8e-10), docetaxel (p = 8.8e-13), etoposide (p = 1.8e-07), and paclitaxel (p = 6.2e-13). In conclusion, we identified and validated a machine learning-based molecular characteristic, IRMLS, which reflects various aspects of the BCa biological process and offers new insights into personalized precision therapy for BCa patients.
膀胱癌(BCa)是一种异质性恶性肿瘤,其特征在于不同的免疫亚型,主要是由于肿瘤浸润免疫细胞及其功能特征的差异。因此,了解BCa中的肿瘤免疫微环境(TIME)格局对于预后预测和指导精准治疗至关重要。在本研究中,我们整合了10种机器学习算法来开发一种免疫相关的机器学习特征(IRMLS),随后创建了一个深度学习模型,用于基于病理图像检测IRMLS亚型。IRMLS被证明是总生存期(OS)的独立预后因素,并表现出强大而稳定的性能(p < 0.01)。高危组表现出免疫炎症表型,与较差的预后和更高水平的免疫细胞浸润相关。我们进一步研究了IRMLS模型内的癌症免疫循环和突变格局,证实高危组对免疫检查点免疫疗法(ICI)和顺铂(p = 2.8e-10)、多西他赛(p = 8.8e-13)、依托泊苷(p = 1.8e-07)和紫杉醇(p = 6.2e-13)辅助化疗更敏感。总之,我们识别并验证了一种基于机器学习的分子特征IRMLS,它反映了BCa生物学过程的各个方面,并为BCa患者的个性化精准治疗提供了新的见解。