Institut Gustave Roussy, Villejuif, France.
Institut National de la Santé Et de la Recherche Médicale (INSERM) U1015, Equipe Labellisée-Ligue Nationale contre le Cancer, Villejuif, France.
EMBO Mol Med. 2021 Jan 11;13(1):e12850. doi: 10.15252/emmm.202012850. Epub 2020 Dec 29.
Decision making in immuno-oncology is pivotal to adapt therapy to the tumor microenvironment (TME) of the patient among the numerous options of monoclonal antibodies or small molecules. Predicting the best combinatorial regimen remains an unmet medical need. Here, we report a multiplex functional and dynamic immuno-assay based on the capacity of the TME to respond to ex vivo stimulation with twelve immunomodulators including immune checkpoint inhibitors (ICI) in 43 human primary tumors. This "in sitro" (in situ/in vitro) assay has the potential to predict unresponsiveness to anti-PD-1 mAbs, and to detect the most appropriate and personalized combinatorial regimen. Prospective clinical trials are awaited to validate this in sitro assay.
免疫肿瘤学中的决策对于根据患者肿瘤微环境(TME)选择众多单克隆抗体或小分子药物的治疗方案至关重要。预测最佳联合治疗方案仍然是一个未满足的医疗需求。在这里,我们报告了一种基于 TME 对十二种免疫调节剂(包括免疫检查点抑制剂(ICI))的体外刺激反应能力的多功能和动态免疫分析方法,该方法在 43 个人类原发性肿瘤中进行。这种“原位”(in situ/in vitro)分析方法有可能预测对抗 PD-1 mAb 的无反应性,并检测最合适和个性化的联合治疗方案。期待进行前瞻性临床试验来验证这种原位分析方法。