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durvalumab 维持治疗在不可切除局部晚期非小细胞肺癌同期放化疗后肺损伤的预测因素。

Predictors of lung injury during durvalumab maintenance therapy following concurrent chemoradiotherapy in unresectable locally advanced non-small cell lung carcinoma.

机构信息

Respiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.

Department of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

出版信息

Thorac Cancer. 2023 Sep;14(25):2601-2607. doi: 10.1111/1759-7714.15042. Epub 2023 Aug 2.

DOI:10.1111/1759-7714.15042
PMID:37533115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10481134/
Abstract

BACKGROUND

Based on the results of the PACIFIC trial, maintenance with durvalumab has emerged as the standard treatment following concurrent chemoradiotherapy in patients with unresectable locally advanced non-small cell lung carcinoma (NSCLC). However, adverse events attributed to durvalumab, especially lung injuries, including immune-related adverse events, and radiation pneumonitis, are concerning. This study retrospectively investigated the factors related to lung injury in patients receiving the PACIFIC regimen.

METHODS

Patients with unresectable locally advanced NSCLC who received durvalumab maintenance therapy following concurrent chemoradiotherapy at Yokohama City University Medical Centre between July 2018 and March 2022 were included. Clinical data, volume of normal lung receiving 20 or 5 Gy or more (V20 or V5), planning target volume (PTV), and relative lung parenchyma volume in emphysematous lung receiving 20 or 5 Gy or more (RLPV20 or 5; V20 or V5/100-percentage of low-attenuation volume) were evaluated.

RESULTS

Performance status (PS), V20, V5, PTV, RLPV20, and RLPV5 were significantly higher in the lung injury group in the univariate analysis. Furthermore, RLPV20 was the most significant factor in the lung injury group in the multivariate analysis comprising PS, PTV, V20, and RLPV20.

CONCLUSION

RLPV20 and RLPV5 are useful in estimating lung inflammation. RLPV20 could be considered the most reliable risk factor for maintenance therapy with durvalumab following concurrent chemoradiotherapy in patients with unresectable locally advanced NSCLC.

摘要

背景

基于 PACIFIC 试验的结果,在不可切除的局部晚期非小细胞肺癌(NSCLC)患者中,durvalumab 的维持治疗已成为同步放化疗后的标准治疗。然而,durvalumab 引起的不良反应,特别是肺部损伤,包括免疫相关不良事件和放射性肺炎,令人担忧。本研究回顾性调查了接受 PACIFIC 方案治疗的患者肺部损伤相关因素。

方法

纳入 2018 年 7 月至 2022 年 3 月在横滨市立大学医学中心接受同步放化疗后接受 durvalumab 维持治疗的不可切除的局部晚期 NSCLC 患者。评估临床数据、接受 20 或 5Gy 或更高剂量照射的正常肺体积(V20 或 V5)、计划靶区(PTV)和接受 20 或 5Gy 或更高剂量照射的肺气肿肺相对肺实质体积(RLPV20 或 5;V20 或 V5/低衰减体积百分比)。

结果

在单因素分析中,肺损伤组的表现状态(PS)、V20、V5、PTV、RLPV20 和 RLPV5 显著更高。此外,在包括 PS、PTV、V20 和 RLPV20 在内的多因素分析中,RLPV20 是肺损伤组的最显著因素。

结论

RLPV20 和 RLPV5 可用于估计肺部炎症。RLPV20 可被认为是不可切除的局部晚期 NSCLC 患者接受同步放化疗后接受 durvalumab 维持治疗的最可靠的危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b441/10481134/ff68a6c1dedf/TCA-14-2601-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b441/10481134/741276468d92/TCA-14-2601-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b441/10481134/b91bcb7c3bf6/TCA-14-2601-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b441/10481134/ff68a6c1dedf/TCA-14-2601-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b441/10481134/741276468d92/TCA-14-2601-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b441/10481134/b91bcb7c3bf6/TCA-14-2601-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b441/10481134/ff68a6c1dedf/TCA-14-2601-g003.jpg

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