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早期非小细胞肺癌立体定向体部放疗后的心脏剂量与生存率

Cardiac Dose and Survival After Stereotactic Body Radiotherapy for Early-stage Non-Small-cell Lung Cancer.

作者信息

Tembhekar Amode R, Wright Cari L, Daly Megan E

机构信息

Department of Radiation Oncology, University of California, Davis, Comprehensive Cancer Center, Sacramento, CA.

Department of Radiation Oncology, University of California, Davis, Comprehensive Cancer Center, Sacramento, CA.

出版信息

Clin Lung Cancer. 2017 May;18(3):293-298. doi: 10.1016/j.cllc.2016.12.007. Epub 2016 Dec 22.

Abstract

INTRODUCTION

Recent analyses have identified cardiac dose as an important predictor of overall survival (OS) after chemoradiation for locally advanced non-small-cell lung cancer (NSCLC). However, the survival influence of the cardiac dose after stereotactic body radiotherapy (SBRT) is unknown. We performed a dose-volume histogram (DVH) analysis of patients treated with SBRT for early stage NSCLC to examine survival and cardiac toxicity.

MATERIALS AND METHODS

We reviewed the medical records of patients who had undergone SBRT for early-stage NSCLC from June 2007 to June 2015 and documented the cardiac DVH parameters, including the maximum and mean dose and percentage of volume receiving >5, >10, >20, and >30 Gy (V5, V10, V20, and V30, respectively). The biologically effective doses and 2-Gy equivalent doses were also calculated. The DVH parameters were assessed as predictors of OS using Cox regression analysis.

RESULTS

We identified 102 patients with 118 treated tumors. At a median follow-up period of 27.2 months (range, 9.8-72.5 months), the 2-year OS estimate was 70.4%. The cardiac DVH parameters were as follows: maximum dose, median, 14.2 Gy (range, 0.3-77.8 Gy); mean dose, median, 1.6 Gy (range, 0-12.6 Gy); and V5, median, 8.7% (range, 0%-96.4%). We identified no correlation between OS and any cardiac dose parameter. No patient developed acute (within 3 months) cardiac toxicity. Four patients died of cardiac causes; all had had preexisting heart disease.

CONCLUSION

In our cohort, cardiac dose was not a predictor of OS after lung SBRT, despite a subset of patients receiving high maximum cardiac doses. The findings from our limited cohort showed that high doses to small volumes of the heart appear safe. Analyses of larger patient cohorts with longer follow-up durations are needed to better delineate the safe cardiac DVH constraints for SBRT.

摘要

引言

最近的分析已确定心脏剂量是局部晚期非小细胞肺癌(NSCLC)放化疗后总生存期(OS)的重要预测指标。然而,立体定向体部放疗(SBRT)后心脏剂量对生存期的影响尚不清楚。我们对接受SBRT治疗的早期NSCLC患者进行了剂量体积直方图(DVH)分析,以研究生存期和心脏毒性。

材料与方法

我们回顾了2007年6月至2015年6月期间接受SBRT治疗的早期NSCLC患者的病历,并记录了心脏DVH参数,包括最大剂量、平均剂量以及接受>5、>10、>20和>30 Gy(分别为V5、V10、V20和V30)的体积百分比。还计算了生物等效剂量和2-Gy等效剂量。使用Cox回归分析评估DVH参数作为OS的预测指标。

结果

我们确定了102例患者,共治疗118个肿瘤。中位随访期为27.2个月(范围9.8 - 72.5个月),2年OS估计值为70.4%。心脏DVH参数如下:最大剂量,中位数为14.2 Gy(范围0.3 - 77.8 Gy);平均剂量,中位数为1.6 Gy(范围0 - 12.6 Gy);V5,中位数为8.7%(范围0% - 96.4%)。我们未发现OS与任何心脏剂量参数之间存在相关性。没有患者发生急性(3个月内)心脏毒性。4例患者死于心脏原因;所有患者均有基础心脏病。

结论

在我们的队列中,尽管部分患者接受了较高的心脏最大剂量,但心脏剂量并非肺SBRT后OS的预测指标。我们有限队列的研究结果表明,小体积心脏接受高剂量似乎是安全的。需要对更大的患者队列进行更长时间的随访分析,以更好地确定SBRT安全的心脏DVH限制。

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