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免疫治疗时代肺癌的确定性调强质子再照射

Definitive intensity modulated proton re-irradiation for lung cancer in the immunotherapy era.

作者信息

Janopaul-Naylor James R, Cao Yichun, McCall Neal S, Switchenko Jeffrey M, Tian Sibo, Chen Haijian, Stokes William A, Kesarwala Aparna H, McDonald Mark W, Shelton Joseph W, Bradley Jeffrey D, Higgins Kristin A

机构信息

Winship Cancer Institute, Department of Radiation Oncology, Emory University School of Medicine, Atlanta, GA, United States.

Biostatistics Shared Resource, Winship Cancer Institute, Emory University, Atlanta, GA, United States.

出版信息

Front Oncol. 2023 Jan 17;12:1074675. doi: 10.3389/fonc.2022.1074675. eCollection 2022.

Abstract

INTRODUCTION

As immunotherapy has improved distant metastasis-free survival (DMFS) in Non-Small Cell Lung Cancer (NSCLC), isolated locoregional recurrences have increased. However, management of locoregional recurrences can be challenging. We report our institutional experience with definitive intent re-irradiation using Intensity Modulated Proton Therapy (IMPT).

METHOD

Retrospective cohort study of recurrent or second primary NSCLC or LS-SCLC treated with IMPT. Kaplan-Meier method and log-rank test were used for time-to-event analyses.

RESULTS

22 patients were treated from 2019 to 2021. After first course of radiation (median 60 Gy, range 45-70 Gy), 45% received adjuvant immunotherapy. IMPT re-irradiation began a median of 28.2 months (8.8-172.9 months) after initial radiotherapy. The median IMPT dose was 60 GyE (44-60 GyE). 36% received concurrent chemotherapy with IMPT and 18% received immunotherapy after IMPT. The median patient's IMPT lung mean dose was 5.3 GyE (0.9-13.9 GyE) and 5 patients had cumulative esophagus max dose >100 GyE with 1-year overall survival (OS) 68%, 1-year local control 80%, 1-year progression free survival 45%, and 1-year DMFS 60%. Higher IMPT (HR 1.4; 95% CI 1.1-1.7, p=0.01) and initial radiotherapy mean lung doses (HR 1.3; 95% CI 1.0-1.6, p=0.04) were associated with worse OS. Two patients developed Grade 3 pneumonitis or dermatitis, one patient developed Grade 2 pneumonitis, and seven patients developed Grade 1 toxicity. There were no Grade 4 or 5 toxicities.

DISCUSSION

Definitive IMPT re-irradiation for lung cancer can prolong disease control with limited toxicity, particularly in the immunotherapy era.

摘要

引言

随着免疫疗法改善了非小细胞肺癌(NSCLC)的无远处转移生存期(DMFS),孤立的局部区域复发有所增加。然而,局部区域复发的管理可能具有挑战性。我们报告了我们机构使用调强质子治疗(IMPT)进行根治性再照射的经验。

方法

对接受IMPT治疗的复发性或第二原发性NSCLC或LS-SCLC进行回顾性队列研究。采用Kaplan-Meier方法和对数秩检验进行事件发生时间分析。

结果

2019年至2021年期间治疗了22例患者。在第一疗程放疗后(中位剂量60 Gy,范围45-70 Gy),45%的患者接受了辅助免疫治疗。IMPT再照射在初始放疗后中位28.2个月(8.8-172.9个月)开始。IMPT的中位剂量为60 GyE(44-60 GyE)。36%的患者在IMPT期间接受了同步化疗,18%的患者在IMPT后接受了免疫治疗。患者的IMPT肺部平均剂量中位值为5.3 GyE(0.9-13.9 GyE),5例患者食管累积最大剂量>100 GyE,1年总生存期(OS)为68%,1年局部控制率为80%,1年无进展生存期为45%,1年DMFS为60%。较高的IMPT剂量(HR 1.4;95%CI 1.1-1.7,p=0.01)和初始放疗肺部平均剂量(HR 1.3;95%CI 1.0-1.6,p=0.04)与较差的OS相关。2例患者发生3级肺炎或皮炎,1例患者发生2级肺炎,7例患者发生1级毒性反应。无4级或5级毒性反应。

讨论

肺癌的根治性IMPT再照射可以在毒性有限的情况下延长疾病控制时间,尤其是在免疫治疗时代。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c199/9888533/151ef405b1c8/fonc-12-1074675-g001.jpg

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