Houston Methodist Research Institute, Houston, Texas.
Immune Monitoring core, Houston Methodist Research Institute, Houston, Texas.
Cancer Res Commun. 2022 Aug 29;2(8):884-893. doi: 10.1158/2767-9764.CRC-22-0057. eCollection 2022 Aug.
Tumors accumulated with infiltrated immune cells (hot tumors) have a higher response rate to immune checkpoint blockade, when compared with those with minimal T-cell infiltration (cold tumors). We report here that patients with lung cancer with different racial backgrounds harbored distinct immune cell profiles in the tumor microenvironment. Compared with African Americans (AA), Caucasian Americans (CA) exhibited increased immune cell infiltration and vasculature, and increased survival. Changes of survival and immune profile were most pronounced among active smokers and nonsmokers, compared with former smokers and total patients. Neighborhood analysis showed that immune cells accumulated around cancer cells in CAs but not AAs. Our findings reveal intrinsic biological differences between AA and CA patients with lung cancer, suggesting that treatment plans should be tailored for patients with different racial backgrounds.
We report biological racial differences among patients with lung cancer where Caucasians present a hot tumor microenvironment compared with cold tumor in AAs. Treatment plans should be customized to maximize therapeutic outcomes.
背景:与 T 细胞浸润最小的肿瘤(冷肿瘤)相比,浸润免疫细胞的肿瘤(热肿瘤)对免疫检查点阻断的反应率更高。我们在此报告,具有不同种族背景的肺癌患者在肿瘤微环境中存在不同的免疫细胞特征。与非裔美国人(AA)相比,白种人(CA)表现出更高的免疫细胞浸润和血管生成,以及更高的生存率。与前吸烟者和所有患者相比,在吸烟者和不吸烟者中,生存和免疫特征的变化最为显著。邻里分析显示,在 CA 中,免疫细胞聚集在癌细胞周围,但在 AA 中没有。我们的研究结果揭示了肺癌 AA 和 CA 患者之间的内在生物学差异,表明治疗计划应针对不同种族背景的患者进行个体化。
意义:我们报告了肺癌患者之间的生物学种族差异,与 AA 中的冷肿瘤相比,CA 患者的肿瘤微环境呈现为热肿瘤。治疗计划应定制以最大限度地提高治疗效果。