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局部晚期非小细胞肺癌的根治性大分割放疗:文献系统综述

Radical-intent hypofractionated radiotherapy for locally advanced non-small-cell lung cancer: a systematic review of the literature.

作者信息

Kaster Tyler S, Yaremko Brian, Palma David A, Rodrigues George B

机构信息

Department of Radiation Oncology, Western University, London, Ontario; Faculty of Medicine, University of Ottawa, Ottawa, Ontario.

Department of Radiation Oncology, Western University, London, Ontario.

出版信息

Clin Lung Cancer. 2015 Mar;16(2):71-9. doi: 10.1016/j.cllc.2014.08.002. Epub 2014 Sep 28.

Abstract

PURPOSE

To identify survival and toxicity characteristics associated with radical-intent hypofractionated radiotherapy for the treatment of stage III non-small-cell lung cancer (NSCLC).

MATERIALS AND METHODS

Relevant studies were identified from a systematic PubMed search of articles published between January 1990 and January 2014. All studies were peer reviewed and included both retrospective and prospective studies of NSCLC patients being treated with radical hypofractionated radiotherapy. Data on overall survival (OS) and toxicity were extracted from each of the studies where available.

RESULTS

Of 685 studies initially identified by the search, a total of 33 studies were found to be relevant and were included in this systematic review. The number of fractions ranged from 15 to 35, the dose per fraction ranged from 2.3 to 3.5 Gy, and the delivered dose ranged from 45.0 to 85.5 Gy. Fifteen of the studies included concurrent chemotherapy, while 18 did not. OS was found to be associated with tumor biological effective dose, with the Pearson correlation coefficient ranging from 0.34 to 0.48. For both concurrent and nonconcurrent chemoradiotherapy acute pulmonary, late esophageal and late pulmonary incidences of toxicity ranged from 1.2% to 12.2%, but had 95% confidence intervals that included zero. The greatest incidence of toxicity was acute esophageal toxicity at 14.9% (95% confidence interval, 0.7%, 29.1%).

CONCLUSIONS

There is a moderate linear relationship between biological effective dose and OS, and greater acute esophageal toxicity with concurrent chemotherapy. Improving outcomes in stage III NSCLC may involve some form of hypofractionation in the context of systemic concurrent therapy.

摘要

目的

确定与根治性大分割放疗治疗Ⅲ期非小细胞肺癌(NSCLC)相关的生存和毒性特征。

材料与方法

通过对1990年1月至2014年1月发表在PubMed上的文章进行系统检索,确定相关研究。所有研究均经过同行评审,包括对接受根治性大分割放疗的NSCLC患者的回顾性和前瞻性研究。在可行的情况下,从每项研究中提取总生存(OS)和毒性数据。

结果

在检索最初确定的685项研究中,共发现33项相关研究并纳入本系统评价。分割次数范围为15至35次,每次分割剂量范围为2.3至3.5 Gy,总剂量范围为45.0至85.5 Gy。15项研究包括同步化疗,18项未包括。发现OS与肿瘤生物等效剂量相关,Pearson相关系数范围为0.34至0.48。对于同步和非同步放化疗,急性肺部、晚期食管和晚期肺部毒性发生率范围为1.2%至12.2%,但95%置信区间包含零。毒性发生率最高的是急性食管毒性,为14.9%(95%置信区间,0.7%,29.1%)。

结论

生物等效剂量与OS之间存在中度线性关系,同步化疗时急性食管毒性更大。改善Ⅲ期NSCLC的治疗效果可能需要在全身同步治疗的背景下采用某种形式的大分割放疗。

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