Department of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
West China School of Medicine, West China Hospital, Sichuan University, Chengdu, China.
Front Immunol. 2022 Jun 24;13:872991. doi: 10.3389/fimmu.2022.872991. eCollection 2022.
Nowadays, platinum-based therapy has been widely used as the first-line therapy of ovarian cancer. However, the effect of the tumor microenvironment on platinum-based therapy remains unclear. In this study, we aim to investigate the relationship between immune microenvironment subtypes and the prognosis of platinum-based therapy in ovarian cancer.
We integrated 565 ovarian cancer samples from two datasets and obtained the immune subtypes (ISs) by consistent clustering of 1190 immune-related gene expressions. The proportional hazards regression model was used to assess the relationship between ISs and the prognosis of platinum-based adjuvant therapy including progression-free survival (PFS) and overall survival (OS). The prognostic contribution of ISs was validated in three additional cohorts. Non-parametric tests were used to assess genomic characteristics, the proportion of immune cells, and immune-related signature differences among ISs.
We identified and validated five ISs associated with different clinical outcomes of the platinum-based adjuvant therapy in ovarian cancer patients. These differences were only found in OS rather than PFS. An immune subtype had the worst OS. Those patients mainly derived from the mesenchymal subtype had the lowest tumor purity with a high leukocyte fraction as well as stromal fraction and had the highest TGF-β response signaling. By contrast, an immune subtype characterized by immunoreactive status with the highest CD8+T cell infiltration and elevated IFN-γ response signaling had the best prognosis. Other subtypes with more diverse immunologic features such as lowest macrophage regulation signaling showed intermediate prognoses. Notably, the contribution of ISs to OS was independent of the clinical response to platinum-based drugs.
Our analysis revealed the association between different immune characteristics and platinum-based adjuvant therapy, indicating the combination of ISs and chemotherapy could optimize the treatment strategy of OC patients.
目前,铂类药物治疗已广泛应用于卵巢癌的一线治疗。然而,肿瘤微环境对铂类药物治疗的影响尚不清楚。本研究旨在探讨卵巢癌免疫微环境亚型与铂类药物治疗预后的关系。
我们整合了两个数据集的 565 个卵巢癌样本,并通过对 1190 个免疫相关基因表达的一致聚类获得了免疫亚型(IS)。比例风险回归模型用于评估 IS 与铂类辅助治疗的预后(包括无进展生存期(PFS)和总生存期(OS))之间的关系。在另外三个队列中验证了 ISs 的预后贡献。非参数检验用于评估 IS 之间的基因组特征、免疫细胞比例和免疫相关特征的差异。
我们鉴定并验证了与卵巢癌患者铂类辅助治疗不同临床结局相关的五个 IS。这些差异仅在 OS 中发现,而在 PFS 中未发现。一种免疫亚型的 OS 最差。这些患者主要来自间充质亚型,肿瘤纯度最低,白细胞分数、基质分数高,TGF-β反应信号最强。相比之下,具有免疫反应状态特征、CD8+T 细胞浸润最高、IFN-γ反应信号升高的免疫亚型预后最佳。其他具有更多免疫特征的亚型,如巨噬细胞调节信号最低,预后中等。值得注意的是,ISs 对 OS 的贡献独立于对铂类药物的临床反应。
我们的分析揭示了不同免疫特征与铂类辅助治疗之间的关联,表明 ISs 与化疗的联合应用可以优化 OC 患者的治疗策略。