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Chemoradioimmunotherapy of inoperable stage III non-small cell lung cancer: immunological rationale and current clinical trials establishing a novel multimodal strategy

机译:III阶段不可操作的非小细胞肺癌的化学咪唑疗法:免疫理由和现行临床试验,建立一种新型多模态策略

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Immune-checkpoint inhibitors (ICI) have dramatically changed the landscape of lung cancer treatment. Preclinical studies investigating combination of ICI with radiation show a synergistic improvement of tumor control probability and have resulted in the development of novel therapeutic strategies. For advanced non-small cell lung cancer (NSCLC), targeting immune checkpoint pathways has proven to be less toxic with more durable treatment response than conventional chemotherapy. In inoperable Stage III NSCLC, consolidation immune checkpoint inhibition with the PD-L1 inhibitor durvalumab after completion of concurrent platinum-based chemoradiotherapy resulted in remarkable improvement of progression-free and overall survival. This new tri-modal therapy has become a new treatment standard. Development of predictive biomarkers and improvement of patient selection and monitoring is the next step in order to identify patients most likely to derive maximal benefit from this new multimodal approach. In this review, we discuss the immunological rationale and current trials investigating chemoradioimmunotherapy for inoperable stage III NSCLC.
机译:免疫检查点抑制剂(ICI)显着改变了肺癌治疗的景观。研究ICI与辐射组合的临床前研究表明肿瘤控制概率的协同改善,并导致新颖的治疗策略的发展。对于先进的非小细胞肺癌(NSCLC),靶向免疫检查点途径已被证明具有比常规化疗更耐用的治疗响应毒性更低。在III阶段III阶段III阶段III阶段,在完成同时铂的化学疗法完成后,通过PD-L1抑制剂Durvalumab进行固结免疫检查点抑制导致无进展和整体存活的显着提高。这种新的三种模式治疗已成为一种新的治疗标准。预测生物标志物的发展和患者选择和监测的改善是下一步,以识别最有可能从这种新的多式联法方法获得最大益处的患者。在本综述中,我们讨论了对III阶段III NSCLC无法操作的阶段III阶段的ChemoRadioImMunurapy的免疫学理论和目前试验。

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