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肿瘤比例评分>90%的非小细胞肺癌可能会增加免疫检查点抑制剂一线治疗中严重免疫相关不良事件的风险:一项回顾性单中心研究。

Non-small cell lung cancer with tumor proportion score > 90% could increase the risk of severe immune-related adverse events in first-line treatments with immune checkpoint inhibitors: A retrospective single-center study.

机构信息

Department of Thoracic Oncology, National Hospital Organization Osaka Toneyama Medical Center, Toyonaka City, Japan.

出版信息

Thorac Cancer. 2022 Sep;13(17):2450-2458. doi: 10.1111/1759-7714.14576. Epub 2022 Jul 12.

DOI:10.1111/1759-7714.14576
PMID:35820673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9436681/
Abstract

BACKGROUND

Since 2015, immune checkpoint inhibitors have been a clinical treatment strategy for patients with advanced or recurrent non-small cell lung cancer (NSCLC). However, the relationship between immune-related adverse event (irAE) risk factors and patient clinical characteristics is unclear. This study aimed to evaluate the relationship between irAE risk and the clinical characteristics of patients with NSCLC.

METHODS

We included patients with advanced or recurrent NSCLC with known programmed death-ligand 1 expression levels treated with immune checkpoint inhibitors. We retrospectively examined the medical records of 260 patients with NSCLC (March 2016-November 2020) and analyzed the relationship between the patient clinical characteristics and irAEs.

RESULTS

Our retrospective analysis revealed that tumor proportion score (TPS) ≥ 90% and adenocarcinoma histology were independent risk factors for irAEs (odds ratio: 3.750 95% confidence interval [CI]: 1.58-8.89 and 0.424 95% CI: 0.19-0.97, respectively) in first-line treatment. However, in patients receiving second- or later-line treatments, no clinical characteristics were identified as risk factors for irAEs. Furthermore, no difference was observed in the response rates to first-line treatments between the TPS ≥ 90% and TPS < 90% groups (74% vs. 71%, p = 0.83). In later-line treatments, the TPS ≥ 90% group had a better response rate than the TPS < 90% group (55% vs. 17%, p < 0.05). However, no significant differences in overall survival were observed in either of the groups.

CONCLUSIONS

TPS ≥ 90% and adenocarcinoma histology were independent risk factors for irAEs in previously untreated patients with advanced or recurrent NSCLC. Therefore, patients at high risk of irAEs require additional monitoring.

摘要

背景

自 2015 年以来,免疫检查点抑制剂已成为晚期或复发性非小细胞肺癌(NSCLC)患者的临床治疗策略。然而,免疫相关不良事件(irAE)风险因素与患者临床特征之间的关系尚不清楚。本研究旨在评估 irAE 风险与 NSCLC 患者临床特征之间的关系。

方法

我们纳入了接受免疫检查点抑制剂治疗的已知程序性死亡配体 1 表达水平的晚期或复发性 NSCLC 患者。我们回顾性检查了 260 例 NSCLC 患者(2016 年 3 月至 2020 年 11 月)的病历,并分析了患者临床特征与 irAEs 之间的关系。

结果

我们的回顾性分析显示,肿瘤比例评分(TPS)≥90%和腺癌组织学是一线治疗中发生 irAEs 的独立危险因素(优势比:3.750,95%置信区间[CI]:1.58-8.89 和 0.424,95%CI:0.19-0.97)。然而,在接受二线或更后线治疗的患者中,没有临床特征被确定为 irAEs 的危险因素。此外,TPS≥90%和 TPS<90%两组之间的一线治疗反应率无差异(74%比 71%,p=0.83)。在更后线治疗中,TPS≥90%组的反应率优于 TPS<90%组(55%比 17%,p<0.05)。然而,两组的总生存均无显著差异。

结论

TPS≥90%和腺癌组织学是非小细胞肺癌患者发生 irAEs 的独立危险因素。因此,高 irAE 风险的患者需要额外的监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e13/9436681/6a21f3406ef1/TCA-13-2450-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e13/9436681/82a856e072f8/TCA-13-2450-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e13/9436681/6a21f3406ef1/TCA-13-2450-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e13/9436681/82a856e072f8/TCA-13-2450-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e13/9436681/6a21f3406ef1/TCA-13-2450-g003.jpg

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