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放化疗后序贯度伐利尤单抗治疗局部晚期非小细胞肺癌患者放射性肺炎的剂量学预测因素。

Dosimetric predictors of pneumonitis in locally advanced non-small cell lung cancer patients treated with chemoradiation followed by durvalumab.

机构信息

Departments of Radiation Oncology and Biostatistics & Information, Mayo Clinic, 200 1st St SW, Rochester, MN, USA.

Departments of Biostatistics & Information, Mayo Clinic, 200 1st St SW, Rochester, MN, USA.

出版信息

Lung Cancer. 2022 Aug;170:58-64. doi: 10.1016/j.lungcan.2022.06.003. Epub 2022 Jun 13.

Abstract

OBJECTIVES

The incidence and predictors of pneumonitis for patients with unresectable, locally advanced non-small cell lung cancer (NSCLC) in the era of consolidation durvalumab have yet to be fully elucidated. In this large single institution analysis, we report the incidence of and factors associated with grade 2 + pneumonitis in NSCLC patients treated with the PACIFIC regimen.

MATERIALS AND METHODS

We identified all patients treated at our institution with definitive CRT followed by durvalumab from 2018 to 2021. Clinical documentation and imaging studies were reviewed to determine grade 2 + pneumonitis events, which required the following: 1) pulmonary symptoms warranting prolonged steroid taper, oxygen dependence, and/or hospital admission and 2) radiographic findings consistent with pneumonitis.

RESULTS

One-hundred ninety patients were included. The majority received 60 Gray (Gy) in 30 fractions with concurrent carboplatin and paclitaxel. Median number of durvalumab cycles received was 12 (IQR: 4-22). At a median follow-up of 14.8 months, 50 (26.3%) patients experienced grade 2 + pneumonitis with a 1-year cumulative incidence of 27.8% (95% CI: 21.9-35.4). Seventeen (8.9%) patients experienced grade 3 + pneumonitis and 4 grade 5 (2.1%). Dosimetric predictors of pneumonitis included ipsilateral and total lung volume receiving 5 Gy or greater (V5Gy), V10Gy, V20Gy, V40Gy, and mean dose and contralateral V40Gy. Heart V5Gy, V10Gy, and mean dose were also significant variables. Overall survival estimates at 1 and 3 years were 87.4% (95% CI: 82.4-92.8) and 60.3% (95% CI: 47.9-74.4), respectively.

CONCLUSION

We report a risk of pneumonitis higher than that seen on RTOG 0617 and comparable to the PACIFIC study. Multiple lung and heart dosimetric factors were predictive of pneumonitis.

摘要

目的

在巩固 durvalumab 治疗时代,尚未充分阐明不可切除局部晚期非小细胞肺癌 (NSCLC) 患者发生肺炎的发生率和预测因素。在这项大型单机构分析中,我们报告了 PACIFIC 方案治疗 NSCLC 患者中 2+级肺炎的发生率和相关因素。

材料和方法

我们确定了 2018 年至 2021 年在我们机构接受确定性 CRT 加 durvalumab 治疗的所有患者。临床记录和影像学研究被回顾以确定 2+级肺炎事件,这些事件需要以下情况:1)需要延长类固醇减量、氧依赖和/或住院治疗的肺部症状,以及 2)与肺炎一致的影像学表现。

结果

190 例患者入组。大多数患者接受 60 Gy 分 30 次照射,同时给予卡铂和紫杉醇。接受 durvalumab 治疗的中位数周期数为 12(IQR:4-22)。中位随访 14.8 个月时,50 例(26.3%)患者发生 2+级肺炎,1 年累积发生率为 27.8%(95%CI:21.9-35.4)。17 例(8.9%)患者发生 3+级肺炎,4 例(2.1%)发生 5 级肺炎。肺炎的剂量学预测因素包括同侧和全肺接受 5 Gy 或更大(V5Gy)、V10Gy、V20Gy、V40Gy、平均剂量和对侧 V40Gy。心脏 V5Gy、V10Gy 和平均剂量也是重要的变量。1 年和 3 年的总生存率估计值分别为 87.4%(95%CI:82.4-92.8)和 60.3%(95%CI:47.9-74.4)。

结论

我们报告的肺炎风险高于 RTOG 0617 所见,与 PACIFIC 研究相当。多个肺和心脏剂量学因素与肺炎相关。

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