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Late course accelerated hyperfractionation radiotherapy for locally advanced esophageal squamous cell carcinoma.

Authors :
Meng MB
Jiang C
Tian LJ
Liu CL
Zhuang HQ
Chen ZJ
Song YC
Wang J
Pang QS
Zhao LJ
Yuan ZY
Wang P
Source :
Thoracic cancer [Thorac Cancer] 2013 May; Vol. 4 (2), pp. 174-185.
Publication Year :
2013

Abstract

Background: Late course accelerated hyperfractionation radiotherapy (LCAHR) is used as a standard treatment option for locally advanced esophageal squamous cell carcinoma (LAESCC) in China, but concerns remain regarding its efficacy and safety. The purpose of this paper was to evaluate the efficacy and safety of LCAHR. The comparisons examined were as follows: LCAHR versus conventional fractionation radiotherapy (CFR) and LCAHR plus chemotherapy (CT) versus LCAHR alone.<br />Methods: We searched the Cochrane Library, MEDLINE, EMBASE, CENTRAL, CBMdisc, and CNKI, as well as employing manual searches. The primary end points were survival and local control. The second end point was toxicities.<br />Results: Based on search criteria, we found 29 trials involving 3187 patients. Our results showed that LCAHR, compared with CFR, improved the survival and local control, and was, thus, more therapeutically beneficial. Further analysis revealed that LCAHR plus CT proved to be better for patients' survival and local control compared to LCAHR alone. Acute toxicities were increased rather than late toxicities.<br />Conclusions: There was a significant survival and local control benefit of LCAHR over CFR, as well as LCAHR plus CT over LCAHR alone. Considering the strength of the evidence, the results of this study indicate that this regimen would be a new promising modality worth further investigation.<br /> (© 2012 Tianjin Lung Cancer Institute and Wiley Publishing Asia Pty Ltd.)

Details

Language :
English
ISSN :
1759-7714
Volume :
4
Issue :
2
Database :
MEDLINE
Journal :
Thoracic cancer
Publication Type :
Academic Journal
Accession number :
28920199
Full Text :
https://doi.org/10.1111/j.1759-7714.2012.00166.x