Department of Medical Oncology, BC Cancer, Vancouver, BC V5Z 4E6, Canada.
Department of Medical Oncology, BC Cancer, Surrey, BC V3V 1Z2, Canada.
Curr Oncol. 2024 Mar 30;31(4):1865-1875. doi: 10.3390/curroncol31040140.
Immune checkpoint inhibitors (ICIs) are increasingly used in the treatment of many tumor types, and durable responses can be observed in select populations. However, patients may exhibit significant immune-related adverse events (irAEs) that may lead to morbidity. There is limited information on whether the presence of specific germline mutations may highlight those at elevated risk of irAEs. We evaluated 117 patients with metastatic solid tumors or hematologic malignancies who underwent genomic analysis through the ongoing Personalized OncoGenomics (POG) program at BC Cancer and received an ICI during their treatment history. Charts were reviewed for irAEs. Whole genome sequencing of a fresh biopsy and matched normal specimens (blood) was performed at the time of POG enrollment. Notably, we found that MHC class I alleles in the HLA-B27 family, which have been previously associated with autoimmune conditions, were associated with grade 3 hepatitis and pneumonitis (q = 0.007) in patients treated with combination PD-1/PD-L1 and CTLA-4 inhibitors, and PD-1 inhibitors in combination with IDO-1 inhibitors. These data highlight that some patients may have a genetic predisposition to developing irAEs.
免疫检查点抑制剂 (ICIs) 在许多肿瘤类型的治疗中越来越多地被使用,并且在选择人群中可以观察到持久的反应。然而,患者可能会出现严重的免疫相关不良事件 (irAEs),这可能导致发病率增加。关于特定种系突变的存在是否可能突出那些患有 irAEs 风险升高的患者,信息有限。我们评估了 117 名患有转移性实体瘤或血液恶性肿瘤的患者,他们通过 BC 癌症的正在进行的个性化肿瘤基因组学 (POG) 计划进行了基因组分析,并在治疗期间接受了 ICI。对 irAEs 进行了图表审查。在 POG 入组时对新鲜活检和匹配的正常标本(血液)进行了全基因组测序。值得注意的是,我们发现 HLA-B27 家族中的 MHC 类 I 等位基因与自身免疫性疾病有关,与接受 PD-1/PD-L1 和 CTLA-4 抑制剂联合治疗以及 PD-1 抑制剂与 IDO-1 抑制剂联合治疗的患者的 3 级肝炎和肺炎有关(q = 0.007)。这些数据表明,一些患者可能存在发生 irAEs 的遗传易感性。