晚期癌症免疫检查点抑制剂失效后的应对措施:专家意见和综述。

Expert review of respiratory medicine Pub Date : 2023-07-01 Epub Date: 2023-10-27 DOI:10.1080/17476348.2023.2268509
Alberto Giuseppe Agostara, Laura Roazzi, Federica Villa, Rebecca Romano', Daniele Piscazzi, Francesca Martinelli, Gabriele Ciarlo, Sara Oresti, Francesca Travaglini, Alessandro Marando, Andrea Sartore Bianchi, Laura Giannetta, Giulio Cerea, Salvatore Siena, Elio Gregory Pizzutilo, Diego Signorelli
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摘要

简介:免疫检查点抑制剂(IO)显著改善了非致癌成瘾性癌症(NSCLC)患者的预后,成为晚期疾病的一线药物。然而,耐药性仍然是一个重大的临床挑战,限制了它们的有效性。涵盖领域:在此,我们讨论了IO治疗后进展的NSCLC患者的标准和创新治疗方法,讨论了新出现的耐药性机制和正在进行的克服这些机制的努力。为了提供对此事的完整概述,我们在PubMed、EMBASE(医学数据库摘录)和Cochrane图书馆等知名数据库中进行了全面的文献检索,并对clinicaltrials.gov上正在进行的主要研究进行了研究,尤其是在治疗失败的时间和进行性疾病的负担方面,应结合患者的临床情况,指导最佳的后续治疗。IO的长期反应者可能受益于IO在进展之外的持续,并结合其他治疗。早期进展的患者应在临床条件保留的情况下进行抢救性CT治疗。最后,对于在相当长的时间内对IO有反应并随后出现寡进展的患者,可以采用多模式方法进行治疗,以最大限度地提高免疫疗法的效益。
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What to do after immune-checkpoint inhibitors failure in advanced non-small cell lung cancer: an expert opinion and review.

Introduction: Immune-checkpoint inhibitors (IO) have significantly improved outcomes of patients with non-oncogene-addicted non-small cell lung cancer (NSCLC), becoming the first-line agents for advanced disease. However, resistance remains a significant clinical challenge, limiting their effectiveness.

Areas covered: Hereby, we addressed standard and innovative therapeutic approaches for NSCLC patients experiencing progression after IO treatment, discussing the emerging resistance mechanisms and the ongoing efforts to overcome them. In order to provide a complete overview of the matter, we performed a comprehensive literature search across prominent databases, including PubMed, EMBASE (Excerpta Medica dataBASE), and the Cochrane Library, and a research of the main ongoing studies on clinicaltrials.gov.

Expert opinion: The dynamics of progression to IO, especially in terms of time to treatment failure and burden of progressive disease, should guide the best subsequent management, together with patient clinical conditions. Long-responders to IO might benefit from continuation of IO beyond-progression, in combination with other treatments. Patients who experience early progression should be treated with salvage CT in case of preserved clinical conditions. Finally, patients who respond to IO for a considerable timeframe and who later present oligo-progression could be treated with a multimodal approach in order to maximize the benefit of immunotherapy.

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