Standard fractionation intensity modulated radiation therapy (IMRT) of primary and recurrent glioblastoma multiforme

被引:39
作者
Fuller, Clifton D. [1 ,2 ,3 ]
Choi, Mehee [1 ]
Forthuber, Britta [4 ]
Wang, Samuel J. [3 ]
Rajagiriyil, Nancy [5 ]
Salter, Bill J. [6 ]
Fuss, Martin [1 ,3 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Radiat Oncol, San Antonio, TX 78229 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Radiol, Grad Div Radiol Sci, San Antonio, TX 78229 USA
[3] Oregon Hlth & Sci Univ, Dept Radiat Med, Portland, OR 97201 USA
[4] Univ Innsbruck, Dept Radio Oncol, A-6020 Innsbruck, Austria
[5] Univ Texas Southwestern Med Sch, Dept Internal Med, Dallas, TX USA
[6] Univ Utah, Hlth Sci Ctr, Dept Radiat Oncol, Salt Lake City, UT USA
关键词
D O I
10.1186/1748-717X-2-26
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Intensity-modulated radiation therapy (IMRT) affords unparalleled capacity to deliver conformal radiation doses to tumors in the central nervous system. However, to date, there are few reported outcomes from using IMRT, either alone or as a boost technique, for standard fractionation radiotherapy for glioblastoma multiforme (GBM). Methods: Forty-two patients were treated with IMRT alone (72%) or as a boost (28%) after 3-dimensional conformal radiation therapy (3D-CRT). Thirty-three patients with primary disease and 9 patients with recurrent tumors were included. Thirty-four patients (81%) had surgery, with gross tumor resection in 13 patients (36%); 22 patients (53%) received chemo-radiotherapy. The median total radiation dose for all patients was 60 Gy with a range from 30.6 to 74 Gy. Standard fractions of 1.8 Gy/day to 2.0 Gy/day were utilized. Results: Median survival was 8.7 months, with 37 patients (88%) deceased at last contact. Nonparametric analysis showed no survival difference in IMRT-boost vs. IMRT-only groups. Conclusion: While technically feasible, preliminary results suggest delivering standard radiation doses by IMRT did not improve survival outcomes in this series compared to historical controls. In light of this lack of a survival benefit and the costs associated with use of IMRT, future prospective trials are needed to evaluate non-survival endpoints such as quality of life and functional preservation. Short of such evidence, the use of IMRT for treatment of GBM needs to be carefully rationalized.
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页数:7
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