Current status of immune checkpoint inhibition in early-stage NSCLC

医学 肿瘤科 耐受性 杜瓦卢马布 放射治疗 内科学 肺癌 免疫疗法 无容量 化疗 放化疗 免疫检查点 阶段(地层学) 癌症 不利影响 古生物学 生物
作者
Johan Vansteenkiste,Els Wauters,Bart Reymen,Christoph Ackermann,Solange Peters,Dirk De Ruysscher
出处
期刊:Annals of Oncology [Elsevier BV]
卷期号:30 (8): 1244-1253 被引量:116
标识
DOI:10.1093/annonc/mdz175
摘要

Immune checkpoint inhibition (ICI) immunotherapy has revolutionized the approach to metastatic non-small-cell lung cancer (NSCLC). In particular, antibodies blocking the inhibitory immune checkpoints programmed death 1 (PD-1) and its ligand (PD-L1) are associated with higher response rates, improved overall survival and better tolerability as compared with conventional cytotoxic chemotherapy. Recently, ICI has moved from the second-line to the first-line setting for many patients with non-oncogene-addicted NSCLC, either alone or in combination with chemotherapy. The next logical step is to examine this therapy in patients with non-metastatic NSCLC to improve long-term overall survival and cure rates. For patients with unresectable stage III NSCLC, ICI with durvalumab after concurrent chemoradiotherapy has brought a major improvement in 2-year progression-free and overall survival, which holds promise for an improved cure rate. As the relapse pattern in patients with completely resected early-stage NSCLC is predominantly systemic, high expectations rest on the integration of ICI therapy in their treatment approach. A large number of studies with adjuvant or neo-adjuvant ICI are ongoing and will be discussed here. The advent of stereotactic ablative radiotherapy has brought a valid alternative treatment of patients unfit for or not willing to undergo surgery. Data on combining systemic therapy and stereotactic ablative radiotherapy are virtually non-existent, but there is a strong biological rationale to combine radiotherapy and ICI therapy. Early findings in small feasibility studies are promising and now need to be explored in well-designed phase III trials.
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