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系统评价新辅助免疫治疗非小细胞肺癌患者的疗效。

Systematic Review of Neoadjuvant Immunotherapy for Patients With Non-Small Cell Lung Cancer.

机构信息

Department of Cardiothoracic Surgery, Royal Prince Alfred Hospital, Sydney University, Sydney, Australia; Chris O'Brien Lifehouse Hospital, Sydney, Australia.

Department of Cardiothoracic Surgery, Royal Prince Alfred Hospital, Sydney University, Sydney, Australia.

出版信息

Semin Thorac Cardiovasc Surg. 2021 Autumn;33(3):850-857. doi: 10.1053/j.semtcvs.2020.12.012. Epub 2021 Jan 12.

Abstract

There is a paucity of robust clinical evidence for the role of neoadjuvant immunotherapy in patients with resectable non-small cell lung cancer. The primary aim of the study was to identify the available data on the feasibility, safety and efficacy of neoadjuvant immunotherapy. A systematic review was conducted using electronic databases. Relevant studies were identified according to predefined selection criteria. Five relevant publications on 4 completed trials were identified. In most studies, >90% of patients were able to undergo surgery within the planned timeframe after neoadjuvant immunotherapy. There was a high incidence of open thoracotomy procedures, either planned or converted from a planned minimally invasive approach. Mortality ranged from 0 to 5%, but none of the reported deaths were considered directly treatment-related. Morbidities were reported according to adverse events related to neoadjuvant systemic therapy, and postoperative surgical complications. Survival outcomes were limited due to short follow-up periods. Major pathologic response ranged from 40.5 to 56.7%, whilst complete pathologic response of the primary tumor ranged from 15 to 33%. Radiological responses were reported according to RECIST criteria and fluorodeoxyglucose-avidity. This systematic review reported safe perioperative outcomes of patients who underwent resection following neoadjuvant immunotherapy. However, there was a relatively high incidence of open thoracotomy procedures, partly due to the technical challenges associated with increased fibrosis and inflammation of tissue, as well as the more advanced stages of disease in patients enrolled in the studies. Future studies should focus on identifying predictors of pathological response.

摘要

新辅助免疫治疗在可切除的非小细胞肺癌患者中的作用缺乏强有力的临床证据。本研究的主要目的是确定新辅助免疫治疗的可行性、安全性和有效性的现有数据。使用电子数据库进行了系统评价。根据预设的选择标准确定了相关研究。确定了 4 项已完成试验的 5 篇相关出版物。在大多数研究中,>90%的患者在新辅助免疫治疗后能够在计划的时间内进行手术。开胸手术的发生率很高,无论是计划中的还是从计划的微创方法转换而来的。死亡率从 0 到 5%不等,但报告的死亡均与治疗无关。根据与新辅助全身治疗相关的不良事件和术后手术并发症报告了发病率。由于随访时间短,生存结果受到限制。主要病理缓解率为 40.5%至 56.7%,而原发性肿瘤的完全病理缓解率为 15%至 33%。根据 RECIST 标准和氟脱氧葡萄糖活性报告了影像学反应。本系统评价报告了接受新辅助免疫治疗后行切除术患者的安全围手术期结果。然而,开胸手术的发生率相对较高,部分原因是与组织纤维化和炎症增加以及研究中入组患者疾病更晚期相关的技术挑战。未来的研究应侧重于确定病理反应的预测因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/8273189/5349736a34d8/nihms-1696403-f0002.jpg

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