接受一线系统疗法的晚期非小细胞肺癌患者的特异部位反应和抗药性模式

Cancers Pub Date : 2024-06-04 DOI:10.3390/cancers16112136
Lauren Julia Brown, J. Ahn, Bo Gao, Harriet Gee, Adnan Nagrial, Eric Hau, Inês Pires da Silva
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引用次数: 0

摘要

晚期 NSCLC 患者对免疫检查点抑制剂(ICIs)化疗或不化疗的反应各不相同。在NSCLC中,转移部位的分布和对全身治疗组合反应的影响仍鲜为人知。在一项针对接受一线系统治疗的不可切除的 III/IV 期 NSCLC 患者的回顾性队列研究中,我们试图评估转移部位与反应和进展模式之间的关联。我们在两家癌症治疗中心研究了有关人口统计学、肿瘤特征(包括转移部位、大小和体积)、治疗和预后的数据。研究终点包括器官部位特异性反应率、客观反应率(ORR)、无进展生存期(PFS)和总生存期(OS)。共有 285 名患者参与了分析。在一项多变量分析中,骨转移患者的ORR、PFS和OS均有所降低。骨转移患者也更容易出现原发耐药。有骨转移或肝转移的患者在接受 ICIs 与化疗或不接受化疗的情况下,OS 较短,而单独接受化疗的患者则不短,这表明耐药性的产生有免疫学基础。对这些部位的肿瘤微环境进行定向评估,并深入了解器官特异性免疫疗法耐药的驱动因素,对于优化这些患者的新型联合疗法和排序至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Site-Specific Response and Resistance Patterns in Patients with Advanced Non-Small-Cell Lung Cancer Treated with First-Line Systemic Therapy
Patients with advanced NSCLC have heterogenous responses to immune checkpoint inhibitors (ICIs) with or without chemotherapy. In NSCLC, the impact of the distribution of metastatic sites and the response to systemic therapy combinations remain poorly understood. In a retrospective cohort study of patients with unresectable stage III/IV NSCLC who received first-line systemic therapy, we sought to assess the association between the site of metastases with patterns of response and progression. Data regarding demographics, tumour characteristics (including site, size, and volume of metastases), treatment, and outcomes were examined at two cancer care centres. The endpoints included organ site-specific response rate, objective response rate (ORR), progression-free survival (PFS), and overall survival (OS). Two-hundred and eighty-five patients were included in the analysis. In a multivariate analysis, patients with bone metastases had a reduced ORR, PFS, and OS. Primary resistance was also more likely in patients with bone metastases. Patients with bone or liver metastases had a shorter OS when receiving ICIs with or without chemotherapy, but not with chemotherapy alone, suggesting an immunological basis for therapeutic resistance. A directed assessment of the tumour microenvironment in these locations and a deeper understanding of the drivers of organ-specific resistance to immunotherapy are critical to optimise novel combination therapies and sequencing in these patients.
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