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Practical challenges in patients with stage III NSCLC receiving checkpoint inhibitors after chemoradiation

机译:在放化疗后接受检查点抑制剂的III期NSCLC患者的实际挑战

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摘要

NSCLC accounts for 80% of all lung cancer diagnoses, and approximately a third of patients present with locally advanced (stage III) disease [ ]. The optimal therapy for fit patients with unresectable and/or inoperable stage III disease has evolved over the last three decades from radiation alone to sequential chemoradiation (CRT) to concurrent CRT followed by checkpoint inhibitor therapy (CPI). The recently reported PACIFIC trial generated a paradigm shift in the treatment of such patients, with a 3-year overall survival (OS) of 57% for patients receiving consolidation durvalumab compared with 43.5% for those receiving placebo [ ]. Similar outcomes were reported with consolidation pembrolizumab in a Hoosier Cancer Research Network (HCRN) Phase II Trial [ ]. In this article, we explore key clinical challenges that arise when treating patients with consolidation CPI after CRT for patients with stage III NSCLC; namely, the management of CPI-related pneumonitis, timing of consolidation CPI and their role in patients with PD-L1 TPS <1% and distinguishing local progression versus pseudoprogression.
机译:NSCLC占所有肺癌诊断的80%,大约三分之一的患者患有局部晚期(III期)疾病[]。在过去的三十年中,针对患有无法切除和/或无法手术的III期疾病的患者的最佳治疗方法已经从单纯放射治疗,顺序放化疗(CRT)到同时进行的CRT继之以检查点抑制剂治疗(CPI)。最近报道的PACIFIC试验在此类患者的治疗方面产生了范式转变,接受巩固性durvalumab治疗的患者的3年总生存率(OS)为57%,而接受安慰剂的患者为33.5%。在Hoosier癌症研究网络(HCRN)的II期临床试验中报道了巩固性pembrolizumab的相似结果[]。在本文中,我们探讨了III期NSCLC患者接受CRT后合并CPI的患者时所面临的主要临床挑战。即,与CPI相关的肺炎的治疗,巩固CPI的时机及其在PD-L1 TPS <1%的患者中的作用,并区分局部进展与假进展。

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