Radiation therapy for extensive-stage small-cell lung cancer in the era of immunotherapy

医学 放射治疗 肿瘤科 免疫疗法 杜瓦卢马布 内科学 肺癌 临床试验 化疗 阿替唑单抗 癌症 无容量
作者
Yaru Tian,Ji Ma,Xuquan Jing,Xiaoyang Zhai,Yuying Li,Zhijun Guo,Jinming Yu,Hui Zhu
出处
期刊:Cancer Letters [Elsevier BV]
卷期号:541: 215719-215719 被引量:48
标识
DOI:10.1016/j.canlet.2022.215719
摘要

Unlike non-small-cell lung cancer (NSCLC), the progression of small-cell lung cancer (SCLC) is slow. Extensive-stage SCLC (ES-SCLC) is a serious threat to human health, with a 5-year survival rate of <7%. Chemotherapy has been the first-line treatment for the past 30 years. The anti-PD-L1 checkpoint blockades durvalumab and atezolizumab have greatly prolonged overall survival and have become the standard first-line therapy for ES-SCLC since the CASPIAN and IMpower133 trials. In the era of chemotherapy, radiation therapy (RT), including thoracic radiation therapy (TRT) and brain radiation therapy (BRT), has shown clinical effects in randomized and retrospective studies on ES-SCLC. RT-immunotherapy has shown exciting synergistic effects in NSCLC. For ES-SCLC, the clinical effects of combining TRT/BRT with immunotherapy have not yet been systematically explored. In this review, we found that studies on RT-immunotherapy in ES-SCLC are relatively few and limited to early phase studies focusing on toxicity. The efficacy and safety profiles of early phase studies encourage prospective clinical trials. In this review, we discuss the best population, optimum TRT dose, proper TRT time, and strategies for reducing radiation-induced neurotoxicity. Furthermore, we suggest that biomarkers and patient performance status should be fully assessed before RT-immunotherapy treatment. Prospective trials are needed to provide more evidence for RT-immunotherapy applications in ES-SCLC.
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