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地塞米松预处理对肺部立体定向放疗中急性肺毒性的影响

Influence of Dexamethasone Premedication on Acute Lung Toxicity in Lung SBRT.

作者信息

Alite Fiori, Shaikh Parvez M, Mahadevan Anand

机构信息

Department of Radiation Oncology, Geisinger Cancer Institute, Danville, PA, United States.

Department of Radiation Oncology, West Virginia University, Morgantown, WV, United States.

出版信息

Front Oncol. 2022 Feb 28;12:837577. doi: 10.3389/fonc.2022.837577. eCollection 2022.

Abstract

INTRODUCTION

The cooperative group experience of thoracic sterotactic body radiation therapy (SBRT) in medically inoperable patients with early stage non-small cell lung cancer (NSCLC) historically utilized corticosteroid premedication. Patterns of care have been mixed as to whether premedication adds benefit in terms of improved lung toxicity and treatment tolerance.

METHODS

Patients treated for NSCLC from 2014 to 2017 with definitive thoracic SBRT (BED≥100) at a single institution, in a prospectively collected database were evaluated. Pretreatment clinicopathologic characteristics, including Eastern Cooperative Oncology Group (ECOG) performance status, PFT parameters of FEV1, and diffusing capacity for carbon monoxide (DLCO) were collected. Treatment and dosimetric characteristics were collected, and patients were scored as to whether dexamethasone was prescribed and utilized with each fraction. Toxicity was graded on multiple domains including lung as during and 30 days after completion of treatment using Common Terminology Criteria for Adverse Events Version 4. Univariate analysis was performed with Fisher's exact test for categorical variables and two-tailed Student's -test for continuous variables. Multivariate analysis was performed with Cox proportional hazards model to adjust for age, pretreatment DLCO, ECOG, tumor size, central versus peripheral location, and biological effective dose.

RESULTS

A total of 86 patients treated with thoracic SBRT with 54-60 Gy in 3-8 fractions met inclusion criteria, with the majority (70%) receiving 5 fractions. Of these patients, 45 (52%) received 4 mg dexamethasone premedication prior to each fraction of SBRT and 41 (48%) were treated without dexamethasone premedication. Overall acute lung toxicity was low in both groups. Between the two groups of patients, 5/45 (11%) developed grade 2 or higher lung toxicity including hospital admission in the dexamethasone premedication arm vs. 2/41 (5%) without premedication ( = 0.4370, Fisher's exact test). Freedom from acute SBRT lung toxicity was no different between dexamethasone premedication arm and no premedication (Log rank, = 0.45). On multivariate Cox proportional hazard modeling adjusting for age, ECOG, tumor size, central vs. peripheral location, pretreatment DLCO, and BED, there was no difference in freedom from acute lung toxicity without dexamethasone premedication (HR: 0.305; 95% CI: 0.033, 2.792; = 0.293).

CONCLUSIONS

In this retrospective analysis, pretreatment steroid prophylaxis with dexamethasone confers a similar acute toxicity profile and no added clinical benefit to treatment without pretreatment steroid prophylaxis.

摘要

引言

在医学上无法手术的早期非小细胞肺癌(NSCLC)患者中,胸部立体定向体部放射治疗(SBRT)的协作组经验历来采用皮质类固醇预处理。关于预处理在改善肺部毒性和治疗耐受性方面是否有益,护理模式不一。

方法

对2014年至2017年在单一机构接受确定性胸部SBRT(生物等效剂量≥100)治疗的NSCLC患者进行评估,这些患者的数据来自前瞻性收集的数据库。收集治疗前的临床病理特征,包括东部肿瘤协作组(ECOG)体能状态、第一秒用力呼气容积(FEV1)的肺功能测试参数以及一氧化碳弥散量(DLCO)。收集治疗和剂量学特征,并对患者是否在每次分割时开具并使用地塞米松进行评分。使用不良事件通用术语标准第4版对包括肺部在内的多个领域的毒性进行分级,分级时间为治疗期间及治疗完成后30天。对分类变量采用Fisher精确检验进行单因素分析,对连续变量采用双尾Student t检验进行单因素分析。采用Cox比例风险模型进行多因素分析,以调整年龄、治疗前DLCO、ECOG、肿瘤大小、中央与外周位置以及生物等效剂量。

结果

共有86例接受胸部SBRT治疗的患者符合纳入标准,剂量为54 - 60 Gy,分3 - 8次分割,大多数(70%)接受5次分割。在这些患者中,45例(52%)在每次SBRT分割前接受4 mg地塞米松预处理,41例(48%)未接受地塞米松预处理。两组的总体急性肺毒性均较低。两组患者中,地塞米松预处理组有5/45(11%)发生2级或更高等级的肺毒性,包括住院治疗,而未预处理组为2/41(5%)(P = 0.4370,Fisher精确检验)。地塞米松预处理组和未预处理组在急性SBRT肺毒性方面无差异(对数秩检验,P = 0.45)。在对年龄、ECOG、肿瘤大小、中央与外周位置、治疗前DLCO和生物等效剂量进行调整的多因素Cox比例风险模型中,未进行地塞米松预处理时,急性肺毒性的无进展生存率无差异(风险比:0.305;95%置信区间:0.033,2.792;P = 0.293)。

结论

在这项回顾性分析中,地塞米松预处理类固醇预防与未进行预处理类固醇预防相比,具有相似的急性毒性特征,且未带来额外的临床益处。

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